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Greetings and welcome to the United States Transhumanist Party Virtual
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Enlightenment Salon. My name is Jannati Stolieroth the second and
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I am the Chairman of the US Transhumanist Party. Here
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we hold conversations with some of the world's leading thinkers
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in longevity, science, technology, philosophy, and politics. Like the philosophers
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of the Age of Enlightenment, we aim to connect every
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field of human endeavor and arrive at new insights to
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achieve longer lives, greater rationality, and the progress of our civilization. Greetings,
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ladies and gentlemen, and welcome to our US Transhumanist Party
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Virtual Enlightenment Salon. Today we have a special conversation in
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store for you about some emerging scientific research that could
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help to remove ourterial plaque by clearing the nondegradable cholesterol
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that accumulates within cells in the arterial walls. Certainly, the
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cardiovascular disease is still the leading cause of death, and
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if we want to overcome aging and death, this is
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a problem that needs to be fought with a lot
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of the available resources. So joining us today we have
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our Director of Community and Citizen Science and twenty twenty
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four US vice presidential candidate Daniel Tweed. We also have
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doctor Bill Andrews, who is our technology advisor and founder
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and CEO of Sierra Sciences. And we have our Legislative Director,
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Jason Geringer joining us as well. And our special guest
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today is doctor Matthew O'Connor, who also goes by OK.
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He is the CEO of Scientific Affairs at Cyclarity Therapeutics.
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He was awarded his master's degree in neuroscience from Northwestern
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Medical in nineteen ninety nine and his PhD and biochemistry
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from Baylor College of Medicine in two thousand and five.
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His post doctoral research includes work at UC Berkeley on
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muscle stem cells and aging. He is also the former
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vice president of Research at the Sens Research Foundation, where
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he oversaw a broad swath of research projects spanning many
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aspects of rejuvenation biotechnology, from which he authored many papers
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and patents. So Cyclarity Therapeutics and its work will be
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the focus of Matthew's presentation today, and then we'll have
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time for a discussion, some questions, a deeper dive into
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that work. So Matthew, welcome, thank you very much, and
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please feel free to begin your presentation.
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Okay, Thanks so much, Trinnedy, and thanks everyone for coming
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to speak with me today. So thanks for the kind introduction.
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As Jennity said, I co founder of Cyclarity Therapeutics and
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our technology spun out of the Sense Foundation, which is
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now emerged as the Longevity Research Institute, But a few
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years ago we moved up to the Buck Institute for
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Research on Aging up in Nevado, California, which is where
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we are headquartered now. And one main point that I
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want to make big picture about our approach and about
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our technology is that we're remediating something that we believe
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is a fundamental, basic part of the aging process, which
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is part of oxidative stress and oxidative stress to one
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of the fundamental building blocks of life, which is cholesterol.
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And so when we say that we're developing a cardiovasco
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disease drug, really we've developed a drug that tar gets
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a fundamental aging molecule, and we're targeting cardiovascular disease as
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a disease indication first, but I believe that our drug
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will have applications in many aspects of aging and aging
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biology and medicine. So to take a quick step back,
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the type of technology, the technology platform that we're using
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to develop next generation therapeutics at cyclarity is these scavenging molecules,
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and so we developed these scavenging molecules to encapsulate small
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toxic biomolecules that accumulate with age and various cells and
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tissues and then float away with them, and we settled
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on these type of molecule called cyclodextrins. Cyclodextrins are cyclic carbohydrates.
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They've been used in many aspects of industry chemistry over
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Load full transcript
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the years, but most in the last couple of decades.
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In medicine, they've been used mostly as delivery tools to
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deliver drugs as a part of drug formulations. But in
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twenty fifteen, the first cycled extro based drug was approved
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and it was acquired by merk It's now called Britian
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otherwise known as Sugarmaducks, and what it is is it's
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an antidote or reversal agent for a anesthesia agent, a paralytic,
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and so it grabs on to after when you're going
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to get surgery, you get dosed with the paralytics so
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that you don't move around during surgery, and then the
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anesthesiologist gives you Britian after they're done with the surgery,
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and the Britian sweeps through, grabs up all of the paralytic,
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pulls it out of your bloodstream and upee the Britian
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and the paralytic out and you wake up right away
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and you have no side effects from the paralytic and
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you're better off. Britain is a blockbuster drug. It's sold
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one point eight billion dollars last year, which is more
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than all of anesthesia combined. And this is the same
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type of approach that we want to take with our drugs,
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is to make things that are specific for a certain
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target that you don't need any more of. Right, you
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don't need any of that paralytic in your body after
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the surgery is done, so you just get rid of
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all of it, and the optimal amount of it to
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be in your body after the surgery is zero. So
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we developed this the cycled extra in technology, which is
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a dimerization technology where we stick to cycled extrints together.
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And that's pretty much the core of our intellectual property,
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which is the ability to encapsulate whatever it is that
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we build to target with one of our cyclic extrien dimers.
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And we've been granted serve patents in this area. So
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most of what I'll talk about today is targeting the
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oxidized form of cholesterol called seven keto cholesterol. I'll talk
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more about that in a minute. We're also working on
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targeting junk that accumulates in your eye with age and
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causes the major form of macular degeneration. We're also looking
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at nanoplastics, which is a good use case for our technology,
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as well as you know, some other things like an
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asusure reversal, which obviously there's there's many other anesthetics that
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we could build reversal agents for. So we started out
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pretty early on doing some pretty intense computational chemistry with
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cyclodextrins and as opposed to other groups, which there's many
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many groups doing computational chemistry simulations these days, not enough.
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I think it's a growing field and something that everyone
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needs to invest more in. But instead of going really
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general with computational chemistry or specializing in what most people
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specialize in, which is protein either protein protein interactions or
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ligand receptor ligand binding interactions, we focused on an only
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modeling cyclodextrins and their bonding with whatever target that we
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wanted to go after and we do increasing levels of
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sophistication of simulations until we get to the level where
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we can actually predict an affinity constant for a given
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target before we even synthesize it. And now what we're
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doing is layering on AI and machine learning so that
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we can actually take the human out of the process
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of designing the drug and let the AI iterate until
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it comes up with the ideal binding partner for whatever
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kind of molecular junk that we're trying to get rid of.
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So we did a lot of that to come up
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with our lead drug candidate, and then we synthesized a
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number of prototypes and iterated back and forth between the
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chemistry and the bench until we came up with our
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first drug that I'll tell you a little bit more
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about in a minute. But first of let me take
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a step back and talk about the free radical oxidation
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process that causes the kind of oxidized cholesterol that we're
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worried
about. So you've probably all heard free radicals. Free
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radicals have been around aging, medicine and biology for decades,
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and when you have an oxygen free radical, they can
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react with a lot of different molecules in negative ways.
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They can react with your DNA, with your mitochondria. When
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they react with regular cholesterol, which is pictured here in
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yellow in the middle, then you add a oxygen molecule on. Typically,
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so this is a non asomatic process. It's a random process,
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but it's not so random because more often than not,
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the chemistry prefers that it adds it in the seventh position,
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which means that you get seven ketocholesterol or seven KC,
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and I'll sort of use oxidizedcholesterol or a seven k
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C interchangeably in the rest of my presentation. And so
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oxidized cholesterol has been implicated in many aspects of aging,
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including aging in the eye and liver, aging and brain aging.
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Most of what I'm going to talk about today revolves
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around how it causes atheroscrosis in your blood vessels and
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how it does that. So this a lot of the
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concept behind cholesterol oxidation, how it happens and where it
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happens and when it happens, was worked out. A lot
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of it was working out in the nineties in vitro
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and in mice, but it's only in the last decade
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that we've started to see some really convincing evidence that
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oxidized cholesterol as well associated with cardiovascular disease, which with
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negative outcomes and with severity of disease. So there's a
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growing awareness of oxidized cholesterol's involvement in heart disease and atheroscrosis.
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So how does it do that? So when you get
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a alesion in your blood vessel wall, like a fatty
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streak that you start developing in your teenage years, a macrophage,
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part of your immune system, is supposed to come along
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and eat up that lesion. But when it runs into
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oxidized cholesterol, it can't digest it, and it can't it
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can't recycle it, it can't transport it back out into the bloodstream. Now,
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macrophage is a really good at recycling cholesterol. When they
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get regular cholesterol in the form of LDL, they take
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it apart and then repackage it into HDL and if
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they don't need it, and then return it back into
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circulation where it can go back to your liver for
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recycling back into the rest of the body where you
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might need more cholesterol. But with the oxidized forms of cholesterol,
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it can't do that. It can't do the reverse cholesterol transport,
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and so it just eats more and more of it.
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And this is the oxidized cholesterol as highly toxic and
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it causes the macrophage to start sequestering lipid and balloon
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up into something called the foam cell. And foam cells
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are these big blobby cells. They're kind of LIKEX and
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essence cells. But it's not caused by by the over
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division like with fibroblasts or something like you might have
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heard of, but it's caused by toxicity from things like oxidizedcholesterol.
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And foam cells build plaque. They are the driver of
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the mass of the plaque accumulation that you get, and
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it's an early and continuous stage in the plaque building process.
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What we wanted to do was ask ourselves, could we
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design a drug to specifically bind the common oxidized form
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of cholesterol, could we remove it from cells and tissues,
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and could removing that reverse the foam cell phenotype and
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potentially rescue atheroscrosis. So we built this drug, which we're
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calling udp zeror zero three, which we trained first computationally
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and then synthetically to prefer binding oxidized cholesterol and to
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ignore regular cholesterol, which you need to survive. And so
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we built this first drug and it has a very
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high affinity for the oxidized form of cholesterol and it
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leaves regular cholesterol alone. And we've done a great deal
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of work to characterize this drug and get it ready
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to be a drug. So first up here at the top,
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you have macrophages, just normal healthy macrophages grown, and then
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you give them a little bit of oxidized cholesterol and
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they bloon up into nasty looking foam cells. And then
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when we give our drug, they turn back into healthy
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macrophages without those blobby lipids in their in their cytosols.
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And your quantification of that here.
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So if you go back for a moment, I just
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want to see the quantities here. So it's ten micromolar
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sevn ketocholesterol.
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Yes, yeah, in this particular case. We've done it many
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different permutations of this, many different ways, and you can
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see how how that's working here. And so that's just
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how the macrophages look. How they look better, They look younger, right,
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they were nasty and old looking. But do they go
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back to doing their job? And the answer is yes.
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If you poison them with the oxidized cholesterol, their ability
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to eat, their ability to do phagocytosis drops, and then
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we give them our drug. The phagocytic capabilities come back
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multiple different ways with both human and mouse cells that
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we did this with. Perhaps more importantly I mentioned earlier
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reverse cholesterol transport, and that's a big part of the
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job of the macrophages in your blood vessels is to recycle,
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is to get rid of the excess cholesterol. But when
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you give them oxidized cholesterol, like over here on the left,
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the reverse cholesterol transport activity goes down to almost zero.
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And then when you give our drug, just very briefly
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for a short amount of time, it goes back up
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quite significantly, which we think means that our drug is
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restoring the ability the macrovisions to do their job not
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just in eating, but also in metabolizing cholesterol transporting cholesterol.
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And that's a pretty key aspect of atheroscrosis. So then
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we went through and did a good amount of characterization
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of the phenomenon and looked at gene expression. And I'll
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just show
a few examples from our recent publication on this.
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One is the CD forty seven, which is being targeted
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by a competitor of ours with a therapeutic antibody, which
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is kind of like in a tumor where the tumor
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evades the immune system. The foam cells do the same thing,
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so they turn up this don't eat me signal called
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CD forty seven. And what we've shown is that our
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treatment with our drug brings that back down a bit,
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so that the cells should be able to be cleared,
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the foam cells should be able to be cleared by
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other macrophages. Another, various aspects of lipid transport get done
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regulated and then go back to normal when we treat
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with our drug, and and and then various other aspects
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of inflammation of scavenging genes that are either upregulated or
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downregulated in response to the insult, which is the oxidized cholesterol,
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and then get reverted variously by treatment with our drug.
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Out of the weeds a little bit. What happens to
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animals when you give them our drug, Well, it's it's
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it's still early days with really fully investigating this, but
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this is the most exciting data that I think. I
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think generally that rodent models of cardiovascar disease of atheroscorosis
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are are pretty artificial and unrealistic, and so I don't
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really like them and I don't like working in them.
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But in in normal healthy rats, if you give them
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our drug, our drug is designed to be cleared very
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quickly and to be cleared through the urine. And that's
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exactly what we see. I'm not showing the data here,
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but actually when we dose with our drug, we see
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the target of our drug, wich is the oxidized olesterol
257
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coming out in the urine. And we see it coming
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out in the same time scale as we see our
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drug being excreted in the urine. And so this suggests
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that our drug is doing its job, and it's doing
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it very fast. And so the the animals are are
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peeing out their their oxidized cholesterol within a couple of
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hours of administration of the drug.
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Uh.
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And so this, this story that I just told you,
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was just recently published in the journal athos Crosis. And
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I should add in here that we just a professor
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in the field, without talking to us about it, wrote
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a nice commentary about our paper, and that was just
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published this past week. So we wanted to turn this
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into a clinical stage drunk, so we worked on the
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chemistry and the manufacturing. We scaled the process to kilogram
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scale manufacturing, We made large scale batches, we put it
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into single use sterile files. We had many meetings with
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regulators in many countries in the UK, in the US
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and in Australia. And then earlier this year we launched
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our Phase one clinical trial in Australia. And I'll tell
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you more about that in a minute, but first here's
279
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the leadership of our team, me and Mike Cope, co
280
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founders the company, Noah Rosenberg, the chief medical officer, and
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the clinical advisory board that he recruited to to help
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us turn our drug into into something that could go
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into people. So PK. Shaw was the main guy who
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dissected in the nineteen nineties the cholesterol oxidation process. And
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Steve Nichols is argue, the world's expert on how blaque
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is built. He's got about I think eight hundred publications
287
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on the subject and he is leading our clinical trial
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now in Australia. So we're doing what's called the traditional
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sad MAD trial, which is single ascending dose, multiple ascending
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dose trial. So we've just completed the single ascending dose
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portion of our trial and so healthy volunteers have received
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the highest dose of our drug that we intend ever
293
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to give to humans, and it's preliminarily seems to be safe.
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And now we've started in the first stage of the
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multiple ascending dose. And one innovation that we're doing is
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our
phase one trial is being run in Australia, which
297
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isn't particularly innovative. Probably a third of all phrase phase
298
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one trials are being run in Australia these days because
299
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it's a great place to run early stage clinical trials.
300
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But our trial is actually instead of being run by
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a private company, it's being run by an academic research organization,
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the Victorian Heart Institute, which is headed up by Steve Nichols,
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and he has the country's foremost heart hospital and he's
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it's just we're super lucky. This is the type of
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guy that the big drug companies call to get their
306
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drugs over the final stages, like the help You Little
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Aid drugs in phase three. He's worked on those bempaedoic
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acid he get those approved. So to have somebody like
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him taking an interest in our drug at at such
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an early stage is really we're really lucky to have him.
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So a little bit more detail about the design of
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our trial. We started out at an extraordinarily low dose
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of our drug, only one twenty fifth of what we
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were eventually intending to dose and scale it up until
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we got to where we are now. And we've just
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gotten past which is the highest dose, which is twenty
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five miligram per kilogram of the recipient. And like I said,
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we've started the multiple dose. So of course, the main
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outcome that we're looking for is safety, you know, vital signs, reactions,
320
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hearing tests, looking at the pharmacokinetics, how fast the drug
321
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is cleared from from circulation. And then what I'm most
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excited about and what the data then I'm really looking
323
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forward to seeing in the coming weeks is the pharmaco
324
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dynamics of the target engagement to see if our drug
325
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is actually grabbing the oxidized cholesterol and pulling it out
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of the human patients, out of their blood and into
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their urine. So we already have permission. Another nice thing
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about doing trials in Australia is that they're quite flexible
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with trial design and they've already given us permission once
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if our drug has proven to be safe and healthy
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young volunteers, we can go straight into a what's called
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like a Phase one B type trial in a small
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number of human patients who have coronary artery disease. They
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have plaque in their cornary artery, and we can dose
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them with our drug. We can look for that target engagement,
336
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see if they're peeing out the seven KC. And then
337
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we can look and at blood inflammation markers, which we'd
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expect to go down based on some of the data
339
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that I showed you before, and we can do non
340
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invasive imaging of their plaque using CTA aigrams, look at
341
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their plaque before and after treatment and see if if
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it improves, see if it gets reduced, see if it
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looks less than flamed, that kind of thing. Next is
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our phase two plan, which is a scaled up version
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of exactly what I just described for late stage phase one,
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which will be in about one hundred and fifty patients
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who already have a qute cornary arter disease, and we'll
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look again at the oxide cholesterol in their blood and
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the urine will look at their blood work, see if
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it improves, and do the imaging, and then of course
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we'll monitor them for heart attacks and strokes, and hopefully
352
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that gets better over the short duration of the phase
353
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two trial. So I want to take a little bit
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of a step back before I wrap up and talk.
355
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Just remind you what I said before, which is that
356
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oxided cholesterol plays a role in brain aging because where
357
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do you have the most cholesterol, the highest density of
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cluster in your body, It's in your brain. So we're
359
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looking at using our trug for various aspects of aging
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in dementia. So we're looking at al Shimer's disease, we're
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looking at stroke recovery, and like I said before, we're
362
00:26:16.839 --> 00:26:20.599
interested in macula de generation, and we've recently become interested
363
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in looking at
at liver failure. So we're we've raised
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a good amount of money so far to run our
365
00:26:29.480 --> 00:26:33.240
phase one. We're closing on a round of that now
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and then we're going to start raising money for our
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00:26:36.440 --> 00:26:40.960
phase two as so if anybody listening is interested in
368
00:26:40.960 --> 00:26:47.880
investing in Cyclarity Therapeutics, please please reach me. And we're
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expecting to make a ideal with a large pharma company
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post phase two where we would license out our drug
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UDPS year zero three and basically hand it off to
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a large pharmaceutical partner to shepherd it through phase three
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clinical trials and approval. And marketing and all of that,
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and at that point we expect to have a big
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return for our investors in three or four years. So
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this is the team of amazing people that make this
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happen at at psych Clarity here in California. But we've
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actually got a team of over one hundred collaborators and
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consultants and CROs all around the world and many too
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many to thank here. So I'll stop show my disclaimers
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00:27:47.279 --> 00:27:52.079
and I can stop here and take any questions that
382
00:27:53.119 --> 00:27:53.599
you all have.
383
00:27:54.559 --> 00:27:58.720
Yes, thank you very much Matthew for that very informative presentation,
384
00:27:58.839 --> 00:28:03.519
and we do have some questions from our panel thus far,
385
00:28:03.960 --> 00:28:08.680
So Daniel Tweet wonders, is injection of your drug UDP
386
00:28:09.279 --> 00:28:12.519
zero zero three the only administration route so far? Or
387
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are there other possibilities as well?
388
00:28:14.440 --> 00:28:17.599
There's various aspects of injection that we're looking at. So
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all the data that we have so far and all
390
00:28:21.359 --> 00:28:23.359
the work that we've done so far is intervenous. But
391
00:28:23.440 --> 00:28:29.000
we've tested it in animals subcutaneously and it works very well,
392
00:28:29.480 --> 00:28:33.799
and so we're envisioning that it will eventually be released
393
00:28:33.839 --> 00:28:38.839
as either as subcutaneous or intramuscular injection. It could be
394
00:28:40.039 --> 00:28:44.839
like a patch or a pump. It won't. It's unlikely
395
00:28:44.920 --> 00:28:46.519
to be a pill.
396
00:28:49.039 --> 00:28:54.640
Yes, thank you for that answer. And Bill has two questions.
397
00:28:54.920 --> 00:29:00.359
The first question is why CCTA instead of c I
398
00:29:00.519 --> 00:29:02.559
M T. And Bill, I'll let you elaborate on that
399
00:29:02.720 --> 00:29:08.839
question for the laypersons in the audience just a moment. Bill,
400
00:29:08.880 --> 00:29:09.960
you need to unmute.
401
00:29:12.279 --> 00:29:16.599
Why a CTN G Graham instead of a CIMT since
402
00:29:16.640 --> 00:29:19.519
you're looking at the plaque before it's ruptured.
403
00:29:23.119 --> 00:29:28.319
So the CIMT is generally done by ultrasound and CTA
404
00:29:28.440 --> 00:29:30.599
is done by X ray. Just for the audience, I
405
00:29:30.599 --> 00:29:33.839
know you know this, Bill, And you get a better
406
00:29:33.880 --> 00:29:40.759
resolution with CTA and you can look more more deeply
407
00:29:41.519 --> 00:29:47.480
into more hidden blood vessel walls as opposed to being
408
00:29:47.519 --> 00:29:53.039
somewhat restricted to more surface level blood vessels with ultrasound,
409
00:29:53.720 --> 00:29:59.920
so that the most quantitative And this isn't this is
410
00:30:00.079 --> 00:30:04.559
and all coming from me. It's mostly from a cardiologist who
411
00:30:04.920 --> 00:30:08.279
who insists that that CTA is the gold standard right
412
00:30:08.279 --> 00:30:13.279
now in terms of doing really quantitative measurements, uh, you know,
413
00:30:13.319 --> 00:30:19.279
down to the single percent different measurements in plaque thickness
414
00:30:19.599 --> 00:30:23.720
and also being able to see the fat Attenuation Index
415
00:30:24.279 --> 00:30:30.400
UH and which is how dense the plaque is, which
416
00:30:30.519 --> 00:30:33.319
which tells you a lot about the characteristics. So even
417
00:30:33.359 --> 00:30:36.359
if the plaque volume isn't changing, you can tell if
418
00:30:36.400 --> 00:30:39.200
the plaque is getting ready to rupture or if it's
419
00:30:40.000 --> 00:30:42.240
if it's getting less likely to rupture. And you can
420
00:30:42.279 --> 00:30:46.559
also tell things about the inflammation using ai UH layered
421
00:30:46.559 --> 00:30:49.920
on top of the CTA imaging these days, so there's
422
00:30:49.920 --> 00:30:51.559
a lot a lot of data you can get out
423
00:30:51.559 --> 00:30:53.759
of the ct A. The bad thing is that that
424
00:30:53.759 --> 00:30:56.279
that you're exposed to X rays and it's not as
425
00:30:56.319 --> 00:30:58.559
fast and cheap. I wish we were doing both, and
426
00:30:58.759 --> 00:31:01.480
I'd like to move into doing both at some point
427
00:31:01.519 --> 00:31:02.839
in the not too distant future.
428
00:31:03.640 --> 00:31:06.200
Okay, I was misinformed. I guess about c I t
429
00:31:06.319 --> 00:31:08.160
I know you can only do it on the karateid arteries,
430
00:31:08.799 --> 00:31:12.160
but I was thinking that people.
431
00:31:11.960 --> 00:31:16.960
Are less interested. I get into arguments with with the
432
00:31:17.000 --> 00:31:20.119
you know, vascular surgeons and such about this. They I
433
00:31:20.160 --> 00:31:22.240
think the karated is a great
place just as a
434
00:31:22.279 --> 00:31:25.440
marker to look to see if a drug like ours
435
00:31:25.480 --> 00:31:28.000
is working. But they say, oh, why do you want
436
00:31:28.039 --> 00:31:29.640
to look at the crodit It's so easy to do
437
00:31:30.559 --> 00:31:34.039
to do surgery and fix the crowded artery. Uh, so
438
00:31:34.400 --> 00:31:37.799
you know there's no there's no market for for treating
439
00:31:38.839 --> 00:31:42.359
crowded stenosis, just to you know, go after a major
440
00:31:42.440 --> 00:31:47.599
artery like like the cornary artery. And I agree with
441
00:31:47.680 --> 00:31:50.440
you that it's a really nice, easy place to look
442
00:31:50.839 --> 00:31:54.640
for plaque and see it really easily and non invasively.
443
00:31:54.880 --> 00:31:57.279
But I get kind of shouted down by the cardiologists
444
00:31:57.279 --> 00:31:58.559
when I try to make that argument.
445
00:32:00.039 --> 00:32:03.279
Okay, I was actually super impressed, So I take your
446
00:32:03.279 --> 00:32:07.880
word for PCSK nine inhibitors with statins have been shown
447
00:32:07.920 --> 00:32:11.079
to turn salt plaque into hard plaque. It's hard plaque
448
00:32:11.119 --> 00:32:13.640
can to be still filled with oxidized cholesterol. I'm not
449
00:32:13.680 --> 00:32:17.720
sure about that. And will your psyclogextrons get rid of
450
00:32:17.920 --> 00:32:21.000
oxidated cholesterol in hard plack if it is.
451
00:32:21.000 --> 00:32:26.000
Sort yeah, I don't have I have a I have
452
00:32:26.039 --> 00:32:29.839
an answer for you. I don't have a perfectly scientifically
453
00:32:29.839 --> 00:32:32.079
satisfying answer to you. I was really worried about that
454
00:32:32.160 --> 00:32:35.039
when we first developed our drug, about whether or not
455
00:32:35.079 --> 00:32:36.960
it was going to be able to penetrate plaque at all.
456
00:32:37.319 --> 00:32:41.240
And so we got samples of hardened plaque tissue from
457
00:32:41.359 --> 00:32:46.759
patients that it was taken out of surgically, and we
458
00:32:47.400 --> 00:32:51.359
soaked our drug in hardened plaque tissue and it pulled
459
00:32:51.880 --> 00:32:55.240
tons of oxidz cholesterol out of the hardened plau tissue.
460
00:32:55.279 --> 00:32:58.920
I don't know the mechanism by which it penetrates so well. Uh,
461
00:32:59.119 --> 00:33:02.799
there's there's not a good explanation for why our drug
462
00:33:02.880 --> 00:33:07.759
penetrates hardened plaque tissue well. But in our hands, you know,
463
00:33:07.920 --> 00:33:10.799
very preliminarily, it looks like it does, and so I
464
00:33:10.839 --> 00:33:15.720
am optimistic that it will in patients. But it's something
465
00:33:15.759 --> 00:33:18.039
we need to look into more. And I wish there
466
00:33:18.039 --> 00:33:22.039
were better animal models to look at that kind of question.
467
00:33:22.599 --> 00:33:24.759
Again, I was super so the other question I had
468
00:33:24.839 --> 00:33:27.160
was
just combined with the first one. I was super impressed.
469
00:33:27.200 --> 00:33:30.079
I was asking these questions because I've been led to
470
00:33:30.079 --> 00:33:32.599
believe from some clinical studies that I'm trying to get
471
00:33:32.640 --> 00:33:35.279
going that these were the top things to be doing.
472
00:33:35.720 --> 00:33:39.640
But I'm actually thinking what you're doing here might be
473
00:33:39.640 --> 00:33:44.960
better than PCSK nine inhibitors with statins for reducing plaque.
474
00:33:45.799 --> 00:33:46.079
Yeah.
475
00:33:46.160 --> 00:33:49.680
I mean the problem is that those are what's available today, right,
476
00:33:49.839 --> 00:33:55.680
So what's on the market now are LDL lowering drugs.
477
00:33:56.240 --> 00:34:01.279
Statins and PCSK nine inhibitors and the cananighbors might be
478
00:34:01.359 --> 00:34:03.920
working slightly better than status, but they're both doing basically
479
00:34:03.920 --> 00:34:07.599
the same thing, lowering your LDL cholesterol, which has you know,
480
00:34:07.720 --> 00:34:10.559
this bad reputation as being the bad cholesterol, but you
481
00:34:10.599 --> 00:34:14.840
actually need ald L cholesterol. It's how you distribute cholesterol
482
00:34:14.880 --> 00:34:16.880
through your body. Most of the cells in your body
483
00:34:16.920 --> 00:34:19.480
wouldn't have any cholesterol if it wasn't for LDL cholesterol,
484
00:34:19.480 --> 00:34:21.599
so you can't just get rid of it. That's why
485
00:34:21.599 --> 00:34:23.800
I like the oxidized cholesterol as a target, because the
486
00:34:23.800 --> 00:34:26.159
optimal amount of it and your body is zero. If
487
00:34:26.199 --> 00:34:29.320
I could like get rid of It's like lead, right,
488
00:34:29.360 --> 00:34:33.000
what's the optimal amount of lead in your body? It's zero.
489
00:34:33.119 --> 00:34:34.800
So if you could just get rid of all your
490
00:34:34.880 --> 00:34:36.920
lead and all of your oxide cholesterol, you'd just be
491
00:34:37.000 --> 00:34:40.199
better off. And so that's why I like it as
492
00:34:40.400 --> 00:34:43.519
a drug target. And I think it's it's a progression,
493
00:34:43.559 --> 00:34:47.000
it's the next generation. We're going to start seeing the
494
00:34:47.119 --> 00:34:49.159
LP little A drugs coming out I think in the
495
00:34:49.199 --> 00:34:51.440
next year or two, but those are only going to work,
496
00:34:51.440 --> 00:34:54.760
and it's basically a different kind of LDL cholesterol, and
497
00:34:55.000 --> 00:34:58.000
I think to really move the needle towards reversing disease
498
00:34:58.119 --> 00:35:01.119
rather than just slowing it down, which is basically what
499
00:35:01.199 --> 00:35:04.039
the lipid lowering drugs do, We're going to need something
500
00:35:04.599 --> 00:35:08.239
more aggressive that can reverse disease.
501
00:35:08.639 --> 00:35:10.800
So did you just say you're targeting you have something
502
00:35:10.800 --> 00:35:12.400
that's going to be targeting LP little A.
503
00:35:13.400 --> 00:35:16.440
No, no, No, I was just saying the next big
504
00:35:16.519 --> 00:35:18.920
heart disease drugs that are going to be released. I'm
505
00:35:18.960 --> 00:35:23.480
predicting because there's several big drug companies that have them
506
00:35:23.480 --> 00:35:27.639
in late stage phase three clinical trials and they seem
507
00:35:27.639 --> 00:35:30.960
to be working reasonably well. Are going to be LP
508
00:35:31.079 --> 00:35:35.480
little A lowering drugs, and we will be the next
509
00:35:35.519 --> 00:35:37.920
generation of drugs after those, I believe.
510
00:35:39.920 --> 00:35:45.079
Yes, very interesting. So that gives rise to a hypothetical
511
00:35:45.159 --> 00:35:51.400
question for me. So, if cholesterol exists in the bloodstream
512
00:35:51.480 --> 00:35:54.800
but it doesn't get oxidized, if you take care of
513
00:35:54.840 --> 00:35:59.400
all of the oxidized cholesterol, does the non oxidized cholesterol
514
00:35:59.480 --> 00:36:03.760
pose any risk of atherosclerosis or can the macrophages that
515
00:36:03.840 --> 00:36:08.639
you mentioned digest any other cholesterol to render it harmless.
516
00:36:10.159 --> 00:36:11.760
Yeah, I mean that's a big part of the job
517
00:36:11.800 --> 00:36:15.719
of the macrophage is is to collect the cholesterol and
518
00:36:16.039 --> 00:36:19.760
recycle it send it back to your liver. So that's
519
00:36:19.840 --> 00:36:24.880
what that's what should happen. The issue is that you
520
00:36:25.000 --> 00:36:30.360
always have oxygen free radicals around, so it's just it's
521
00:36:30.400 --> 00:36:33.440
like rusting. It literally is rusting, right, it's the rusting
522
00:36:33.480 --> 00:36:37.519
process of oxygen reacting in this case with cholesterol instead
523
00:36:37.519 --> 00:36:39.480
of like metal on your car or something like that.
524
00:36:39.599 --> 00:36:39.760
Right.
525
00:36:40.599 --> 00:36:44.639
But it's a similar process, and so it's going to
526
00:36:44.719 --> 00:36:49.599
keep happening. And so if you have elevated cholesterol, it's
527
00:36:49.960 --> 00:36:52.679
and you have the same amount of oxidation. If you
528
00:36:52.719 --> 00:36:55.800
increase either oxidation or cholesterol, you're going to end up
529
00:36:55.800 --> 00:37:02.360
with more oxidized cholesterol. So people with elevated cholesterol tend
530
00:37:02.559 --> 00:37:05.880
to have more oxidized cholesterol in their system. It's not
531
00:37:05.920 --> 00:37:08.559
a one to one because you can have more oxidation
532
00:37:08.639 --> 00:37:11.239
in your system for various reasons. And we don't exactly
533
00:37:11.320 --> 00:37:14.519
understand why there are people walking around with like normal
534
00:37:14.599 --> 00:37:17.800
levels of cholesterol but really high levels of oxidized cholesterol.
535
00:37:18.280 --> 00:37:22.360
And is it possible to have the opposite scenario where
536
00:37:22.360 --> 00:37:26.760
someone has high levels of cholesterol overall but low levels
537
00:37:26.760 --> 00:37:29.880
of oxidized cholesterol for whatever reason, or do we not
538
00:37:30.039 --> 00:37:33.519
observe that unless that person has been treated with something
539
00:37:33.719 --> 00:37:35.960
like UDP zero zero three.
540
00:37:36.199 --> 00:37:38.920
You know, there are people who do seem to be
541
00:37:39.039 --> 00:37:43.760
somewhat resistant to walking around with high cholesterol. I don't
542
00:37:43.760 --> 00:37:47.079
think it's well studied enough to say that they aren't
543
00:37:47.119 --> 00:37:52.960
accumulating oxidized cholesterol in various places in their bodies, whether
544
00:37:53.039 --> 00:37:55.960
or not they develop atheroschrosis at a young age like
545
00:37:56.719 --> 00:38:01.199
most of them do. I think they're probably building up
546
00:38:01.199 --> 00:38:06.039
oxized cholesterol someplace where we're not looking, like in the brain,
547
00:38:06.119 --> 00:38:09.519
which is really hard to buyopsy. You can only look
548
00:38:09.559 --> 00:38:13.440
at it pretty much after somebody dies, and other tissues
549
00:38:13.480 --> 00:38:13.920
as well.
550
00:38:15.559 --> 00:38:18.599
Yes, thank you for that answer. And Bill has a question.
551
00:38:19.119 --> 00:38:24.199
Do antioxidants reduce the levels of oxidized cholesterol or can
552
00:38:24.360 --> 00:38:25.960
some antioxidants do that?
553
00:38:28.320 --> 00:38:32.599
You know, I it's something that some groups have looked
554
00:38:32.639 --> 00:38:36.119
into a little bit. It, I mean mostly antioxidants have
555
00:38:36.280 --> 00:38:40.719
been kind of a disappointment in general in medicine and
556
00:38:40.760 --> 00:38:41.760
anti aging medicine.
557
00:38:41.800 --> 00:38:41.960
Right.
558
00:38:41.960 --> 00:38:45.119
They haven't proven to be very effective. Now, the counter
559
00:38:45.199 --> 00:38:48.079
argument to that is that we haven't built good enough
560
00:38:48.440 --> 00:38:52.079
antioxidants yet. We haven't targeted them for the right places
561
00:38:52.360 --> 00:38:56.599
or something like that. So I think there's potential room
562
00:38:56.639 --> 00:39:02.599
for that. But you can't reduce your oxygen free radicals
563
00:39:02.639 --> 00:39:08.480
to zero. You can't like completely prevent all oxygen free
564
00:39:08.519 --> 00:39:12.039
radicals from forming, no matter how many antioxidants you take.
565
00:39:12.280 --> 00:39:15.960
So that's why I follow this kind of damage repair
566
00:39:16.079 --> 00:39:25.280
philosophy philosophy approach. You know, Generally, my approach to studying
567
00:39:25.519 --> 00:39:29.599
and trying to remediate the aging process and and therapeutically
568
00:39:30.079 --> 00:39:31.960
is that I think it's the best place to intervene.
569
00:39:32.039 --> 00:39:36.599
But there is potential to see I haven't seen yet
570
00:39:36.639 --> 00:39:41.599
a
convincing study showing that that there's good antioxidant evidence
571
00:39:41.679 --> 00:39:46.159
showing reduction in oxidized cholesterol levels in a person, but
572
00:39:46.519 --> 00:39:48.480
I don't think it's been studied enough, and I think
573
00:39:48.960 --> 00:39:53.039
better studies with better antioxidants could work to some extent
574
00:39:53.079 --> 00:39:58.920
with it. And perhaps we've started a small project looking
575
00:39:59.000 --> 00:40:02.559
at some kind of combin therapy in that realm, in
576
00:40:02.960 --> 00:40:06.440
a model system that we're looking at that maybe it
577
00:40:06.480 --> 00:40:10.119
could be helpful, especially since you get when you have
578
00:40:10.239 --> 00:40:13.599
high inflammation in someplace like a plaque, you also get
579
00:40:13.679 --> 00:40:18.960
high levels of oxidation and so if you combine, if
580
00:40:19.000 --> 00:40:23.760
you combine antioxidation with getting rid of oxidized cholesterol, maybe
581
00:40:23.760 --> 00:40:25.119
we'll get a synergistic effect.
582
00:40:26.159 --> 00:40:28.920
Very interesting, Thank you very much. And we have a
583
00:40:29.000 --> 00:40:32.400
number of questions from Daniel Tweed as well. Let's start
584
00:40:32.440 --> 00:40:37.360
with the questions that focus on the name of the drug,
585
00:40:37.559 --> 00:40:41.639
and Daniel is curious about the origins of the name
586
00:40:41.719 --> 00:40:44.360
u DP zero zero three. Is that a chemical name
587
00:40:44.400 --> 00:40:45.639
shorthand of some sort.
588
00:40:46.880 --> 00:40:51.880
It's so UDP stands for Underdog Pharmaceuticals, which was the
589
00:40:51.920 --> 00:40:57.039
original name of our company, and then we changed our
590
00:40:57.119 --> 00:41:00.039
company named as Cyclarity Therapeutics a few years ago. So
591
00:41:00.920 --> 00:41:06.079
we just we did the kind of boring but efficient thing,
592
00:41:06.159 --> 00:41:12.719
which was numbering our compounds from starting from one as
593
00:41:12.760 --> 00:41:17.039
we invented them. And yeah, it'll get a more exciting
594
00:41:17.119 --> 00:41:20.280
name at some point. I didn't want to give it
595
00:41:20.480 --> 00:41:25.840
a sexy name too early, because what I see happening
596
00:41:25.960 --> 00:41:28.239
is that you get your favorite name and you name it,
597
00:41:28.280 --> 00:41:30.840
and then you get a partnership or you get a
598
00:41:30.840 --> 00:41:33.159
new big investor and they don't like your name and
599
00:41:33.159 --> 00:41:35.119
they make you change the name. And then you see
600
00:41:35.199 --> 00:41:38.519
drugs go through like three, four or five different names
601
00:41:38.559 --> 00:41:42.079
before they actually get you know, widespread on the market,
602
00:41:42.119 --> 00:41:45.000
and I figured out just wait a little while before we,
603
00:41:45.320 --> 00:41:48.519
you know, get get married to a name. But if
604
00:41:48.519 --> 00:41:52.760
people have ideas for names for us, send them to me,
605
00:41:52.840 --> 00:41:55.719
and we're starting to make a list.
606
00:41:56.719 --> 00:42:02.239
Yes, So for those viewers watching this virtual Enlightenment salon,
607
00:42:02.360 --> 00:42:06.119
please put any ideas you have for a name for
608
00:42:06.679 --> 00:42:10.840
UDP zero zero three that might eventually be used in
609
00:42:11.360 --> 00:42:16.239
our YouTube chat and we will relay them to OK
610
00:42:17.039 --> 00:42:21.159
And in the meantime, Daniel has another question. He notes
611
00:42:21.519 --> 00:42:26.079
this scavenging therapy molecule sounds like it has benefits for
612
00:42:26.360 --> 00:42:30.119
both new as well as long term users, and he
613
00:42:30.199 --> 00:42:33.719
wants to know if that's correct given that this process
614
00:42:33.840 --> 00:42:39.039
of oxidation happens continuously. So would you expect that this
615
00:42:39.119 --> 00:42:42.679
is a drug that could also be administered over the
616
00:42:42.760 --> 00:42:48.280
long term for someone to prevent the formation of atherosclerotic plas.
617
00:42:48.920 --> 00:42:49.159
Yeah.
618
00:42:49.199 --> 00:42:51.920
I think it can be a preventative as well as
619
00:42:52.360 --> 00:42:56.039
a reversal agent. And I hope we see a day
620
00:42:56.280 --> 00:43:01.199
when based on a biomarker task like sized cholesterol in
621
00:43:01.239 --> 00:43:05.360
your blood or in a tissue sample, you can take
622
00:43:05.880 --> 00:43:08.400
our drug and that you don't have to wait until
623
00:43:08.440 --> 00:43:10.960
you're one of your blood vessels is like more than
624
00:43:10.960 --> 00:43:14.000
fifty percent included when you start having trouble you know,
625
00:43:14.039 --> 00:43:16.840
climbing stairs or breathing or getting chest pain or something
626
00:43:16.880 --> 00:43:19.400
like that, or having a know hour attack before you
627
00:43:19.440 --> 00:43:25.360
ever get diagnosed with having atheroscrosis. So yeah, so I
628
00:43:25.360 --> 00:43:28.280
think it can be preventive as well as a reversal.
629
00:43:28.559 --> 00:43:31.880
I don't think that you will need to take it continuously,
630
00:43:32.039 --> 00:43:34.559
like every day or something like that. I think you
631
00:43:34.599 --> 00:43:39.400
can take it intermittently and we hope that you will
632
00:43:39.480 --> 00:43:43.639
just have to take approximately six doses in a row
633
00:43:44.360 --> 00:43:48.000
over a couple of weeks. Our current protocol is over
634
00:43:48.039 --> 00:43:51.639
the course of sixteen days, every third day you get
635
00:43:51.679 --> 00:43:54.079
a dose and that that should get rid of the
636
00:43:54.199 --> 00:43:57.639
vast majority of the oxidzed cholesterol in your system. And
637
00:43:57.679 --> 00:44:00.719
that's taken decades for it to build up. Hopefully you
638
00:44:00.760 --> 00:44:02.400
don't have to come back for another five or ten
639
00:44:02.480 --> 00:44:05.960
years for another course of treatment. So maybe people are
640
00:44:05.960 --> 00:44:11.719
going to start getting this when they're symptomatic in their sixties, say,
641
00:44:12.719 --> 00:44:16.880
but later on, maybe we'll be taking it in you know,
642
00:44:17.000 --> 00:44:20.079
our thirties or forties, every you know, five or ten
643
00:44:20.159 --> 00:44:22.960
years to make sure you don't get sick from that stuff.
644
00:44:23.559 --> 00:44:26.880
Yes, indeed, and would you pair that with some sort
645
00:44:26.960 --> 00:44:32.800
of diagnostic tests, say a blood test to measure the
646
00:44:33.239 --> 00:44:37.719
oxidized cholesterol, the seven keto cholesterol, rather than just the
647
00:44:37.760 --> 00:44:39.840
total cholesterol or the LDL.
648
00:44:40.360 --> 00:44:46.639
Eventually, we're not developing a there's not a commercially available
649
00:44:47.159 --> 00:44:50.559
seven k C. There's two kinds of blood tests you
650
00:44:50.559 --> 00:44:54.760
can do for oxidized cholesterol. One is for oxidized LDL,
651
00:44:55.000 --> 00:44:57.400
which there is a test for and you can you
652
00:44:57.440 --> 00:45:00.880
can go and get Our drug should not not directly
653
00:45:01.599 --> 00:45:07.079
remove ox LDL. Our drug isn't meant to attack LDL
654
00:45:07.239 --> 00:45:11.360
or HDL. It's meant to attack cells and tissues. So
655
00:45:11.480 --> 00:45:14.920
what ox LDL does is it delivers seven k C
656
00:45:15.440 --> 00:45:18.880
to the blood vessel walls and two macrophases, and so
657
00:45:19.000 --> 00:45:22.000
then our drug can go into the macrophages and pull
658
00:45:22.000 --> 00:45:24.599
it out after it's been delivered. So you can get
659
00:45:24.639 --> 00:45:27.360
a test for ox LDL, but our drug shouldn't be
660
00:45:27.719 --> 00:45:32.000
lowering ox l dl. We can test in our clinical trial.
661
00:45:32.000 --> 00:45:36.800
We are testing people for blood and you're in oxidized
662
00:45:36.840 --> 00:45:43.119
cholesterol seven keto cholesterol. But we're not developing a diagnostic
663
00:45:43.679 --> 00:45:47.440
that we're intending to know to release and sell to
664
00:45:47.519 --> 00:45:51.360
the public. I think that the world will be better
665
00:45:51.400 --> 00:45:54.639
off if and when there is such an approved diagnostic.
666
00:45:54.639 --> 00:45:57.280
We're doing a little bit of work trying to invent
667
00:45:57.440 --> 00:46:03.239
a faster, cheaper method of measuring seven keto cholesterol so
668
00:46:03.320 --> 00:46:07.440
that US or somebody else, a diagnostics company could could
669
00:46:07.480 --> 00:46:09.920
take that and turn it into a diagnostic test that
670
00:46:09.960 --> 00:46:14.920
patients could take. To your question about what it will
671
00:46:14.960 --> 00:46:17.239
be paired with when it's first released, it will probably
672
00:46:17.280 --> 00:46:20.800
be paired with with with andiogram. So you'll get a
673
00:46:20.840 --> 00:46:25.000
scan
of your of your say, coronary artery, and it'll
674
00:46:25.039 --> 00:46:27.679
be blocked, and you'll take our drug and you'll come
675
00:46:27.719 --> 00:46:30.519
back in six months or a year and get another
676
00:46:30.599 --> 00:46:34.679
scan and hopefully it will have improved, and maybe it'll
677
00:46:34.679 --> 00:46:36.760
have improved, but it won't have improved as much as
678
00:46:36.760 --> 00:46:38.920
your cardiologist wants, and so they'll give you another course
679
00:46:38.920 --> 00:46:39.440
of treatment.
680
00:46:39.920 --> 00:46:40.039
Uh.
681
00:46:40.199 --> 00:46:42.800
And they could do that, you know, once every year
682
00:46:42.880 --> 00:46:46.639
or so until they're satisfied that you're better. But I
683
00:46:46.760 --> 00:46:49.519
eventually I hope that it gets reduced to an easier
684
00:46:49.559 --> 00:46:55.400
biomarker like a blood test. Yes, thank you.
685
00:46:55.599 --> 00:47:00.480
And that leads into the question from Daniel tweet. How
686
00:47:00.679 --> 00:47:03.960
affordable would this therapy be in vision to.
687
00:47:03.960 --> 00:47:13.079
Be well, we expected to be covered by insurance. We're
688
00:47:13.119 --> 00:47:20.800
planning to two uh to to release it you know
689
00:47:20.840 --> 00:47:25.800
widely in uh in all the you know markets around
690
00:47:25.840 --> 00:47:26.159
the world.
691
00:47:26.760 --> 00:47:26.880
Uh.
692
00:47:27.719 --> 00:47:31.960
It's not going to be you know, uh a dollar
693
00:47:32.079 --> 00:47:34.840
or ten dollars a treatment. It's probably going to be
694
00:47:36.119 --> 00:47:39.719
at least a few thousand dollars for a treatment. And
695
00:47:39.800 --> 00:47:43.079
that we don't know the market economics get it's probably
696
00:47:43.079 --> 00:47:45.639
going to be thousands of dollars for a treatment.
697
00:47:46.280 --> 00:47:46.400
Uh.
698
00:47:47.639 --> 00:47:51.800
And but you know, I think that's it's more expensive
699
00:47:51.920 --> 00:47:55.280
than like a statin, but it's going to be cheaper
700
00:47:55.320 --> 00:48:01.199
than a gene therapy or and competitive with the therapeutic antibiodies.
701
00:48:02.440 --> 00:48:05.360
Yes, and as you said, hopefully the few thousand dollars
702
00:48:05.400 --> 00:48:11.920
per treatment will be administered every fairly large number of years,
703
00:48:11.960 --> 00:48:15.639
like five or ten years, rather than say, every year.
704
00:48:15.920 --> 00:48:19.639
So thank you for that answer. And Bill also wonders
705
00:48:19.679 --> 00:48:23.800
with regard to the comment about the angiogram, will you
706
00:48:23.920 --> 00:48:28.480
DP zero zero three reduce clocks also or at least
707
00:48:28.480 --> 00:48:29.840
have that tendency to do that.
708
00:48:30.800 --> 00:48:33.920
Let me say I was miss I was thinking differently
709
00:48:33.920 --> 00:48:36.800
when I asked that question. I was forgetting that regular
710
00:48:36.840 --> 00:48:42.599
angigrams can detect large plaque bulges too, so, but but yeah,
711
00:48:42.840 --> 00:48:45.320
is there any chance that this would help with ruptured
712
00:48:45.360 --> 00:48:47.280
plaques When a clock gets formed.
713
00:48:47.800 --> 00:48:51.960
Our drug acts quickly in terms of removing oxide cholesterol,
714
00:48:51.960 --> 00:48:56.280
but it acts slowly in terms of allowing the macrophage
715
00:48:56.480 --> 00:48:59.320
then to go back to doing its job and cleaning
716
00:48:59.400 --> 00:49:02.280
up the plaque. So our drug isn't designed to work
717
00:49:02.360 --> 00:49:07.880
like draino and flush out your arteries in in minutes.
718
00:49:08.880 --> 00:49:12.199
It's meant to flush out all your oxidized cholesterol and
719
00:49:12.239 --> 00:49:15.119
then for it to heal over the course of weeks
720
00:49:15.119 --> 00:49:19.239
and months. So you wouldn't want to rely on our
721
00:49:19.360 --> 00:49:23.239
drug if you were like in an ambulance needing like
722
00:49:23.280 --> 00:49:28.440
a cloudbuster, you know, because you're the you know, the
723
00:49:28.440 --> 00:49:33.440
blood flow to your brain has been been blocked. That said,
724
00:49:33.719 --> 00:49:39.679
there's clouding, there's clotting that happens inside of plaque, and
725
00:49:39.679 --> 00:49:43.880
and ruptured plaque can get stuck places where it's not
726
00:49:44.239 --> 00:49:49.480
very easy to remove surgically, and you know, sometimes there's
727
00:49:49.519 --> 00:49:52.760
decisions about whether to leave it alone or monitor it,
728
00:49:52.880 --> 00:49:56.159
or go in and remove it. And so in some
729
00:49:56.239 --> 00:50:01.280
of those edge cases where it's where a wait and
730
00:50:01.320 --> 00:50:06.119
see uh approach might work better than maybe our drug
731
00:50:06.119 --> 00:50:08.880
with help. But I'm just sort of I'm kind of
732
00:50:08.960 --> 00:50:10.679
rambling because I'm thinking about this on the flat, because
733
00:50:10.679 --> 00:50:12.360
I haven't thought about that question before.
734
00:50:12.400 --> 00:50:16.079
About There's another question I had, and that's because I
735
00:50:16.119 --> 00:50:18.679
was doing some Google searches while you were answering some
736
00:50:18.719 --> 00:50:23.639
other questions. But on cyclodextrons, I saw that there's two
737
00:50:23.719 --> 00:50:30.480
hydroxy propyle beta cyclodextrin that's already available for getting rid
738
00:50:30.480 --> 00:50:34.440
of oxidized cholesterol. Is that is yours comparable to that?
739
00:50:34.519 --> 00:50:36.360
And it didn't look like that's used as a dimer
740
00:50:36.440 --> 00:50:37.000
like yours is.
741
00:50:38.599 --> 00:50:43.039
Yeah, so what you're Yeah, well, you're the two hydroxypropyle
742
00:50:43.079 --> 00:50:46.599
beta cyclodextrin or just hydroxyprople beta cyclod extrin or h
743
00:50:46.679 --> 00:50:53.079
pbc D. It's been around for decades. It's it's used
744
00:50:53.119 --> 00:50:55.639
in in foods, it's
used in I think it's in
745
00:50:55.679 --> 00:51:00.639
for breeze. It's it's it's used to deliver drugs. It's
746
00:51:00.719 --> 00:51:03.320
it's very safe, you can inject it at very high doses,
747
00:51:03.800 --> 00:51:06.960
you can eat it. There's there's food grid hydroxy public
748
00:51:07.000 --> 00:51:11.360
beta cyclodextra and so should you get injected with it
749
00:51:12.320 --> 00:51:16.360
in order to get treated safe for you know, aging
750
00:51:16.480 --> 00:51:20.079
or atheroschrosis something like that, or or other diseases. There
751
00:51:20.079 --> 00:51:24.000
are actually two companies that are trying to use that
752
00:51:24.719 --> 00:51:28.039
substance to treat Niemann Pick type CE disease, which is
753
00:51:29.000 --> 00:51:33.119
a rare licens almost storage disorder, which is a cholesterol
754
00:51:33.159 --> 00:51:38.719
transporter disorder. Now, hydroxy probably beta cyclodextrin doesn't bind cholesterol
755
00:51:39.199 --> 00:51:41.840
very well at all. It's a very very weak, if
756
00:51:41.880 --> 00:51:45.079
at all, binder of cholesterol. But they figure this stuff
757
00:51:45.119 --> 00:51:47.760
is so safe and it's approved for like anything that
758
00:51:47.800 --> 00:51:51.280
you want to use it for. Uh, So we're going
759
00:51:51.360 --> 00:51:54.679
to take these kids and dose them with like enormous
760
00:51:54.760 --> 00:51:57.079
enormous quantities of this stuff and see if it helps.
761
00:51:57.519 --> 00:51:59.559
Because it did help in animal model. So if you
762
00:51:59.599 --> 00:52:05.079
give an animal with this name and Pick disease, this
763
00:52:06.159 --> 00:52:10.199
hydroxy prople beta cyclduxtrain when they're very young, it helps.
764
00:52:10.480 --> 00:52:13.000
It does help a lot. I suspect it is helping
765
00:52:13.079 --> 00:52:16.760
the patients. It's been a little difficult for these companies
766
00:52:16.800 --> 00:52:19.079
to prove that it's helping because these patients are so
767
00:52:19.280 --> 00:52:23.679
sick and have so much brain damage that it's hard
768
00:52:23.679 --> 00:52:27.760
to tell if they're getting better. I think they're living
769
00:52:27.800 --> 00:52:30.880
longer with a very poor standard of living. I think
770
00:52:30.920 --> 00:52:35.000
the drug is very weak but probably effective at extraordinarily
771
00:52:35.079 --> 00:52:37.960
high doses. And the kind of doses that you need
772
00:52:38.039 --> 00:52:41.440
to make it effective since it's such an inactive compound,
773
00:52:42.000 --> 00:52:44.320
is like having one of these kids trying to lie
774
00:52:44.360 --> 00:52:47.679
still on a table getting a IB for like six
775
00:52:47.719 --> 00:52:51.000
hours or something like that. So I think our drug
776
00:52:51.000 --> 00:52:53.440
would work better for name and Pick disease. We're not
777
00:52:53.719 --> 00:52:56.480
working on that, but I'd love to be working on
778
00:52:56.519 --> 00:53:00.199
that someday. And I think it would be this same
779
00:53:00.320 --> 00:53:04.239
kind of thing if HPbCD could help you with others races,
780
00:53:04.320 --> 00:53:06.440
I think you would need to be getting an IV
781
00:53:06.719 --> 00:53:10.000
bag full of it frequently in order for it to
782
00:53:10.000 --> 00:53:14.079
have an effect. It's just not a drug. It's you know,
783
00:53:14.199 --> 00:53:17.199
it's it's something that is a very weak binder of
784
00:53:17.239 --> 00:53:19.760
a lot of things. So I don't know what else
785
00:53:19.800 --> 00:53:22.199
it's binding when it's going in there, But you know,
786
00:53:22.280 --> 00:53:27.079
it's pretty safe stuff, so it probably doesn't hurt. But
787
00:53:27.440 --> 00:53:31.239
I mean it's been shown to cause hearing loss at
788
00:53:31.400 --> 00:53:33.639
very high doses in rodents, so that's something that some
789
00:53:33.679 --> 00:53:37.039
people are concerned about. You just need to stay clear
790
00:53:37.079 --> 00:53:40.800
of those hearing loss toxic doses.
791
00:53:41.119 --> 00:53:44.719
Interesting. Thank you very much, and we've got a few
792
00:53:44.800 --> 00:53:49.639
questions from Daniel. He wonders could this be used to
793
00:53:49.679 --> 00:53:54.000
externally process a patient's blood in a kind of dialysis
794
00:53:54.079 --> 00:53:57.079
modality or would that not make sense? I think Daniel,
795
00:53:57.119 --> 00:54:02.519
what you're considering is perhaps taking a patient's blood and
796
00:54:02.599 --> 00:54:06.519
applying the drug to it outside of the patient's body
797
00:54:06.559 --> 00:54:10.159
and then doing some sort of like therapeutic plasma exchange
798
00:54:10.199 --> 00:54:13.440
where you pump in the clean blood and replace the
799
00:54:13.519 --> 00:54:17.039
existing blood with it. Or would that not really take
800
00:54:17.079 --> 00:54:21.920
care of the problem, which would be that cholesterol accumulating
801
00:54:21.960 --> 00:54:22.719
in the arteries.
802
00:54:23.119 --> 00:54:26.079
Yeah, it's a good question, and it's something we thought
803
00:54:26.119 --> 00:54:31.039
about for a while. So one problem with the approach
804
00:54:31.280 --> 00:54:35.280
is the last thing that you just said, Jenity, which
805
00:54:35.320 --> 00:54:39.119
is that you could pull all of the oxide. Using
806
00:54:39.159 --> 00:54:40.719
a method like that, you could pull all the oxides
807
00:54:40.760 --> 00:54:43.079
cholesterol out of the blood stream, but you couldn't. You
808
00:54:43.079 --> 00:54:46.400
wouldn't be delivering your drug to the system and letting
809
00:54:46.440 --> 00:54:50.920
our drug go into your blood vessel walls and any
810
00:54:50.960 --> 00:54:54.360
other tissues where it might be able to pull oxide
811
00:54:54.440 --> 00:54:59.000
cholesterol out of now, that doesn't mean we haven't thought
812
00:54:59.039 --> 00:55:00.440
about it and that it might not be a good
813
00:55:00.480 --> 00:55:02.760
therapeutic approach. What we haven't been able to think of
814
00:55:02.800 --> 00:55:06.239
a way to do is, so you know, you take
815
00:55:06.320 --> 00:55:08.559
the drug, you take the blood out of the body,
816
00:55:08.599 --> 00:55:13.679
and then you put our drug in there. Presumably you
817
00:55:13.719 --> 00:55:16.320
want to pull the drug out before putting it back
818
00:55:16.400 --> 00:55:18.519
into the body or else like why did you go
819
00:55:18.599 --> 00:55:21.519
through this process rather than just delivering it into the body.
820
00:55:21.760 --> 00:55:23.840
So we haven't been able to think of a way
821
00:55:24.000 --> 00:55:29.239
to clear our drug out of the blood stream as
822
00:55:29.239 --> 00:55:30.519
a part of that process.
823
00:55:30.679 --> 00:55:30.960
Yet.
824
00:55:31.559 --> 00:55:34.519
If there's people listening who are interested in the in
825
00:55:34.920 --> 00:55:37.280
how that might work, or think they might understand something
826
00:55:37.320 --> 00:55:40.679
about the how to make that work in a kind
827
00:55:40.719 --> 00:55:43.199
of like a sort of a dialysis sort of approach,
828
00:55:43.480 --> 00:55:45.840
we're interested in that as approach, but we haven't started
829
00:55:45.840 --> 00:55:50.039
playing with it yet, but it's it's a cool idea
830
00:55:50.039 --> 00:55:51.320
that we want to work on sometime.
831
00:55:52.599 --> 00:55:56.639
Yes, thank you very much for that answer. And Daniel's
832
00:55:56.639 --> 00:56:00.719
other question is could targeted cyclodextrins be created did using
833
00:56:01.079 --> 00:56:05.800
a suitably genetically engineered cell, such as perhaps an E.
834
00:56:05.880 --> 00:56:09.679
Coli bacterium that could be harnessed for that purpose, like,
835
00:56:09.760 --> 00:56:14.039
could you reconfigure one of those to produce the cyclodextrons.
836
00:56:14.360 --> 00:56:18.880
So the core building blocks are built by by microbes,
837
00:56:19.000 --> 00:56:25.840
but I've never heard of a microbe building a modified cyclodextrin.
838
00:56:26.119 --> 00:56:28.480
Like the example that Bill was asking me about earlier
839
00:56:28.599 --> 00:56:32.119
is a hydroxy propylated cyclodextrin. So you take a hydroxypropyle
840
00:56:32.199 --> 00:56:36.320
chemical group and stick it onto a onto a cyclodextrin.
841
00:56:36.320 --> 00:56:38.599
Which is part of the power of cyclodextrins is how
842
00:56:39.159 --> 00:56:43.519
you could there's potentially hundreds or you know, theoretically infinite
843
00:56:44.119 --> 00:56:46.719
different types of chemical groups that you could stick onto
844
00:56:46.719 --> 00:56:49.880
a cyclodextrin and then a cyclodextrian. There's three different sizes
845
00:56:49.920 --> 00:56:53.280
of cyclodextrians. The cyclodextrins that we're using are the medium size,
846
00:56:53.760 --> 00:56:57.239
and we're making dimers of them. Our dimers have forty
847
00:57:00.639 --> 00:57:05.480
sites on them where you
could potentially put any of
848
00:57:05.519 --> 00:57:08.480
these chemical groups that you want, so they're kind of
849
00:57:08.599 --> 00:57:14.639
infinitely engineerable. Now I've never heard of a microbe figuring
850
00:57:14.679 --> 00:57:18.639
out how to do that chemistry on its own, but
851
00:57:18.679 --> 00:57:21.280
they're very good at producing the core building blocks, and
852
00:57:21.320 --> 00:57:24.360
that's how they're how the building blocks are made that
853
00:57:24.400 --> 00:57:28.719
we buy and then use to do our synthetic chemistry
854
00:57:28.760 --> 00:57:31.920
on top of that, But I've never heard of somebody
855
00:57:31.960 --> 00:57:34.800
figuring out how to how to culture, how to like
856
00:57:34.920 --> 00:57:40.320
grow substituted We call them substituted cyclodextrons like in a vat.
857
00:57:41.880 --> 00:57:47.719
Yes, thank you for that answer. And Daniel wonders, a
858
00:57:47.800 --> 00:57:51.440
dimer is a chemical pairing of identical molecules. Yes, that's
859
00:57:51.519 --> 00:57:56.920
the definition. Essentially, a molecule or molecular complex consisting of
860
00:57:56.920 --> 00:58:00.760
two identical molecules or subunits that are link together.
861
00:58:01.559 --> 00:58:04.639
But you don't necessarily, so you could have the dimer,
862
00:58:04.679 --> 00:58:06.760
and you could imagine that on one side of the
863
00:58:06.800 --> 00:58:11.280
dimer you have one kind of chemistry and on the
864
00:58:11.320 --> 00:58:13.320
other dimer you have another kind of chemistry. And we
865
00:58:13.360 --> 00:58:17.199
can do that kind of chemistry. Uh, when we engineer
866
00:58:17.360 --> 00:58:21.400
our dimers, and that is part of our intellectual property
867
00:58:21.960 --> 00:58:26.079
is making the two different halves different, so that if
868
00:58:26.079 --> 00:58:31.199
you have an asymmetrical target, you could engineer one side
869
00:58:31.599 --> 00:58:36.159
to grab one side of your target in a certain
870
00:58:36.199 --> 00:58:39.360
way and the other side so you could work on
871
00:58:39.719 --> 00:58:41.559
you know, the charge, So if you're looking at a
872
00:58:41.679 --> 00:58:44.800
charged target, you could put the opposite charge on one
873
00:58:44.840 --> 00:58:47.519
side of the cycled extrin and not on the other side.
874
00:58:48.159 --> 00:58:51.039
If if once, if your target is like has like
875
00:58:51.079 --> 00:58:54.199
a skinny and a fat side like that, you could
876
00:58:54.239 --> 00:58:57.119
make your your cycled extra more more narrow on one
877
00:58:57.159 --> 00:58:59.360
side and fatter on the other. Those are all things
878
00:58:59.360 --> 00:59:01.679
that we play with a lot when we're in the
879
00:59:01.760 --> 00:59:05.159
early stages of engineering our cyclic extrons at the computational
880
00:59:05.199 --> 00:59:07.679
and then synthetic level very interesting.
881
00:59:07.719 --> 00:59:11.920
So the dimers are more versatile
than they may appear
882
00:59:12.000 --> 00:59:15.719
at first glance, at least with your approach. Now, one
883
00:59:16.119 --> 00:59:20.119
question that I'm curious about is in regard to your
884
00:59:20.159 --> 00:59:23.280
future plans. In the event that the phase two trials
885
00:59:23.320 --> 00:59:26.039
are successful, you stated you would make a deal with
886
00:59:26.079 --> 00:59:30.679
a large pharma company to essentially manufacture and sell this drug.
887
00:59:31.280 --> 00:59:35.920
Would you plan for a deal where Cyclarity would maintain
888
00:59:36.000 --> 00:59:38.920
the intellectual property and then the pharma company would pay
889
00:59:38.960 --> 00:59:41.320
you royalties over time to use it. Or would you
890
00:59:41.440 --> 00:59:45.280
just sell the intellectual property in one lump sum and
891
00:59:45.440 --> 00:59:49.400
let the pharma company do what it pleases thereafter.
892
00:59:50.039 --> 00:59:53.559
There's a lot of potential ways that could play out,
893
00:59:53.840 --> 00:59:55.599
and you know, I may or may not be in
894
00:59:55.639 --> 00:59:58.320
a position to get my perfect wish. So my perfect
895
00:59:58.360 --> 01:00:03.800
wish is that we would do a partnership with a
896
01:00:03.880 --> 01:00:08.239
large pharma company, either a joint venture where we share
897
01:00:08.320 --> 01:00:12.079
responsibility for the further development, for the carrying out of
898
01:00:12.079 --> 01:00:14.480
the phase three, so that we could have influence over
899
01:00:14.519 --> 01:00:17.400
how the phase three is developed, what kind of patients
900
01:00:17.440 --> 01:00:19.880
it gets used, and how it's being tested so that
901
01:00:19.920 --> 01:00:22.159
they don't mess it up, that kind of thing. And
902
01:00:22.199 --> 01:00:24.519
then you know, going into the marketing, likely the big
903
01:00:24.559 --> 01:00:26.199
pharma company, we do all the marketing, and then we
904
01:00:26.239 --> 01:00:29.239
would get royalties from that. So we would get upfronts
905
01:00:29.280 --> 01:00:32.440
and royalties, likely in either the scenario where it was
906
01:00:32.480 --> 01:00:35.639
a joint venture or where we just sold the drug
907
01:00:35.920 --> 01:00:38.920
to a partner and they just took it over from there.
908
01:00:39.199 --> 01:00:41.400
And then you know, another possibility is that our whole
909
01:00:41.400 --> 01:00:44.760
company would get acquired by a large drug company. That's
910
01:00:45.320 --> 01:00:48.039
not really my favorite idea because what I really want
911
01:00:48.079 --> 01:00:51.679
to do is take the proceeds from that equity event
912
01:00:52.039 --> 01:00:53.840
when they buy the drug from us. So they do
913
01:00:53.880 --> 01:00:56.480
a deal and we get upfronts, and then we pour
914
01:00:56.880 --> 01:01:00.280
that money back into the company, into our platform so
915
01:01:00.280 --> 01:01:03.400
that we can develop our next ten drugs with those funds,
916
01:01:03.480 --> 01:01:06.039
which might not happen if we get acquired.
917
01:01:06.360 --> 01:01:10.519
Yes, indeed, I think it would be a preferable outcome
918
01:01:10.760 --> 01:01:16.079
if you continue to have input and involvement and an
919
01:01:16.119 --> 01:01:21.519
income stream from how that drug gets developed and used,
920
01:01:21.639 --> 01:01:26.280
in particular, because then you could ensure that it actually
921
01:01:26.280 --> 01:01:30.920
gets rolled out to patients. Sometimes pharmaceutical companies will acquire
922
01:01:30.960 --> 01:01:35.519
intellectual property and sit on it, and that's not necessarily
923
01:01:35.920 --> 01:01:41.679
the best outcome for patients who could benefit from the
924
01:01:41.760 --> 01:01:46.159
drug in clinical settings. Bill Wonders, would DP zero zero
925
01:01:46.199 --> 01:01:48.880
three qualify for fast track clinical studies.
926
01:01:49.039 --> 01:01:51.440
I think that to be fast track, it would have
927
01:01:51.480 --> 01:01:55.559
to be rare disease. I am envisioning it more angling
928
01:01:55.599 --> 01:02:01.960
towards accelerated approval, which is what FDA uses for disease indications,
929
01:02:02.039 --> 01:02:06.360
where you may be able to get a tentative approval
930
01:02:06.840 --> 01:02:09.719
and then need to keep doing studies to prove that
931
01:02:09.760 --> 01:02:12.840
you're having the outcome effects like effects on heart attacks
932
01:02:12.920 --> 01:02:15.599
or strokes. That's really my dream for this is that
933
01:02:15.679 --> 01:02:18.400
we would get approved on the basis of plaque regression,
934
01:02:19.039 --> 01:02:22.199
rather than doing what is traditionally done, which is due
935
01:02:22.280 --> 01:02:25.639
like a long five year study with thousands of patients
936
01:02:25.679 --> 01:02:28.599
waiting for people to have heart attacks and strokes, and
937
01:02:28.639 --> 01:02:30.960
then you count bodies and you see if people on
938
01:02:31.000 --> 01:02:34.679
the active group die less or have fewer heart attacks
939
01:02:34.880 --> 01:02:37.239
than the people on the placebo group, which I think
940
01:02:37.320 --> 01:02:39.159
is we're going to look back on those kinds of
941
01:02:39.199 --> 01:02:42.079
studies someday and think they're barbaric. I hope that we
942
01:02:42.199 --> 01:02:45.559
can get accelerated approval on the basis of their plaque
943
01:02:45.599 --> 01:02:49.039
regression and then show the reduction in heart attacks and
944
01:02:49.079 --> 01:02:53.159
strokes in the following years after initial approval.
945
01:02:53.320 --> 01:02:57.559
Yes, indeed, that would definitely be more humane and better
946
01:02:57.599 --> 01:03:00.800
for the patients. So I know we're past the hour.
947
01:03:00.920 --> 01:03:03.280
Do you have time for a couple more questions just
948
01:03:03.360 --> 01:03:04.880
the ones that have been post?
949
01:03:05.039 --> 01:03:07.239
Let's say two more
questions and then I got to run.
950
01:03:07.800 --> 01:03:13.039
All right, So, Daniel Wonders, is the Victorian Hard Institute
951
01:03:13.079 --> 01:03:16.719
funding most or all of the trials now taking place.
952
01:03:17.199 --> 01:03:21.159
No, Cyclarity Therapeutics is funding one hundred percent of the
953
01:03:21.800 --> 01:03:25.880
trials taking place. Almost all of the money has come
954
01:03:25.920 --> 01:03:29.000
from private investment into Cyclarity therapeutics.
955
01:03:29.280 --> 01:03:29.719
All right.
956
01:03:30.119 --> 01:03:34.159
And Daniel's comment, after which I will pose his last question,
957
01:03:34.239 --> 01:03:37.119
is this is almost like a precursor to what cellular
958
01:03:37.239 --> 01:03:40.920
nanomachines might one day accomplish and I hope we all
959
01:03:41.199 --> 01:03:44.880
live to see the day when that happens. And his
960
01:03:45.039 --> 01:03:49.079
final question is he sees that it's interesting that the
961
01:03:49.599 --> 01:03:54.840
blockbuster drug Britian out sells the anesthesia drugs or did
962
01:03:54.880 --> 01:03:59.079
he hear that incorrectly? Does it actually outsell the common
963
01:03:59.119 --> 01:03:59.960
anesthesia drug.
964
01:04:01.159 --> 01:04:05.400
Yeah, it outsells all of anesthesia put together. Now that said,
965
01:04:05.559 --> 01:04:10.400
that's a little bit misleading because Britian is still unpatent
966
01:04:10.599 --> 01:04:13.400
and so Merk can charge a lot of money for it,
967
01:04:13.440 --> 01:04:17.719
whereas most traditionally used anesthesia agents are generic and pretty cheap.
968
01:04:17.760 --> 01:04:20.840
But it's still pretty impressive to me that this one
969
01:04:21.199 --> 01:04:27.000
reversal agent, it's so incredibly valuable and profitable because anesthesiologists
970
01:04:27.119 --> 01:04:31.719
love it. It's incredibly safe and effective, and even if
971
01:04:31.719 --> 01:04:35.800
they accidentally were on purpose, anesthesiologists are getting lazy and
972
01:04:36.400 --> 01:04:40.679
dosing their patients with an excess of Britian. And I
973
01:04:40.760 --> 01:04:43.719
was a study done recently trying to bring them to
974
01:04:43.800 --> 01:04:49.280
task and looking for the consequences of giving your patients
975
01:04:49.320 --> 01:04:53.239
too much Britian, and they couldn't find any consequences from
976
01:04:53.239 --> 01:04:56.480
giving patients, like you know, two or three times as
977
01:04:56.519 --> 01:04:59.760
much Britian as they needed to clear out the paralytics.
978
01:05:00.639 --> 01:05:03.400
The anesthesiologists are just strigging their shoulders and like not
979
01:05:03.480 --> 01:05:05.519
doing the math to figure out exactly how much they
980
01:05:05.519 --> 01:05:08.199
should give their patients and just taking a you know,
981
01:05:08.239 --> 01:05:10.039
a bunch off of the shelf and giving them the
982
01:05:10.039 --> 01:05:13.039
whole bial rather than calculating how much they should be
983
01:05:13.079 --> 01:05:16.000
getting their patient. Because it's it's a next generation drug.
984
01:05:16.039 --> 01:05:19.239
It only grabs onto something bad that you want to
985
01:05:19.280 --> 01:05:22.239
get rid of and then you pee it out and
986
01:05:22.280 --> 01:05:24.639
you pee out you know, whatever extra that you that
987
01:05:24.719 --> 01:05:27.920
you get. So it's really a perfect drug, and you
988
01:05:27.960 --> 01:05:30.320
know that's that's how we want our drug to work
989
01:05:30.360 --> 01:05:30.760
as well.
990
01:05:31.480 --> 01:05:34.719
Yes, that sounds like a great drug essentially no adverse
991
01:05:34.719 --> 01:05:38.400
side effects. So thank you Matthew for all of your
992
01:05:38.440 --> 01:05:41.679
answers and for your time today. That was a fascinating
993
01:05:41.719 --> 01:05:46.519
and enlightening presentation. Do you have any final words for
994
01:05:46.800 --> 01:05:50.519
our audience, any comments that you wish you could have made,
995
01:05:50.800 --> 01:05:53.559
or anything else that you want to say before we close.
996
01:05:54.880 --> 01:05:57.360
I just want to say thanks so much for having
997
01:05:57.400 --> 01:06:00.960
me here to present to the transhuman to a party
998
01:06:01.119 --> 01:06:05.079
and people have more ideas, you know, whether they're about
999
01:06:05.079 --> 01:06:08.039
the name, or about the science, or if you're in
1000
01:06:08.079 --> 01:06:11.440
science and you want to collaborate with Cyclarity, if you
1001
01:06:11.440 --> 01:06:13.440
know you're in a research lab and do you have
1002
01:06:13.480 --> 01:06:15.679
a model system that you think our drug could work in,
1003
01:06:15.719 --> 01:06:18.239
we'd love to collaborate with you and get to the
1004
01:06:18.239 --> 01:06:23.079
finish line together. It takes a huge number of people
1005
01:06:23.199 --> 01:06:27.440
to get a drug approved, and there's so many wonderful
1006
01:06:27.559 --> 01:06:31.719
supporters out there, and I invite everyone to get in touch,
1007
01:06:32.039 --> 01:06:34.800
get in touch with me on LinkedIn, follow up Cyclarity
1008
01:06:34.840 --> 01:06:37.880
on social media, and we'll try to keep you all
1009
01:06:37.960 --> 01:06:39.199
updated on how things are going.
1010
01:06:40.360 --> 01:06:43.760
All right, thank you very much, Okay for your time today.
1011
01:06:44.000 --> 01:06:48.000
This was quite an enlightening presentation. Please to all of
1012
01:06:48.079 --> 01:06:53.360
our viewers, share your ideas with us in the chat
1013
01:06:53.519 --> 01:06:57.719
or reach out to ok and to Cyclarity on social media.
1014
01:06:57.840 --> 01:07:01.280
And I hope that we can all live long and prosper.
1015
01:07:05.360 --> 01:07:05.800
Thank you.
1016
01:07:06.400 --> 01:07:12.760
Indeed, thanks Cody and Ghanadi. We want to get rid
1017
01:07:12.800 --> 01:07:16.880
of this guy. As you know, our purpose here at
1018
01:07:16.880 -->
01:07:24.719
Redfast Revolution against Agent and Death is to kill death. Right, So, uh, Joe,
1019
01:07:25.440 --> 01:07:26.480
how are we going.
1020
01:07:26.360 --> 01:07:26.960
To kill death?
1021
01:07:27.800 --> 01:07:29.480
I mean together, that's the whole thing.
1022
01:07:30.559 --> 01:07:36.880
Together together in a coordinated, collaborative fashion where we feel
1023
01:07:37.280 --> 01:07:39.960
like we feel we feel our life more than we
1024
01:07:40.000 --> 01:07:40.360
feel that.
1025
01:07:42.239 --> 01:07:45.480
Okay, and Cody, how are we going to kill death?
1026
01:07:45.519 --> 01:07:47.840
How is it I mortally is going to kill death?
1027
01:07:47.960 --> 01:07:50.320
Well, everything Joe just said. But also we need to
1028
01:07:50.360 --> 01:07:52.920
free the geniuses of society who are working on the
1029
01:07:52.960 --> 01:07:55.599
science end of it, and we do that together.
1030
01:07:57.559 --> 01:07:59.960
Good, So, Ghannadi tell us your view.
1031
01:08:00.760 --> 01:08:04.039
We need to get the public to recognize that killing
1032
01:08:04.119 --> 01:08:08.000
death is both feasible and desirable. They need to see
1033
01:08:08.039 --> 01:08:12.400
a plausible path for getting from here to there, and
1034
01:08:12.440 --> 01:08:16.039
that's actually one way in which games like lev the
1035
01:08:16.119 --> 01:08:18.640
Game can help to get them to see it's not
1036
01:08:18.720 --> 01:08:21.239
going to be a single moment in time. It's not
1037
01:08:21.279 --> 01:08:24.359
going to be a single magic pill or panacee. It's
1038
01:08:24.359 --> 01:08:27.079
going to be a process. But it's a process that
1039
01:08:27.600 --> 01:08:30.720
each person, even if you're sixty five or seventy five
1040
01:08:30.840 --> 01:08:35.640
or eighty or ninety, has a chance in undergoing successfully.
1041
01:08:37.319 --> 01:08:42.840
Okay, I will play Devil's advocate and I will ask Death, Death,
1042
01:08:42.960 --> 01:08:44.079
what did you think about that?
1043
01:08:44.880 --> 01:08:48.920
I was quite inspired by Joe's talk, and it's been
1044
01:08:49.079 --> 01:08:53.079
quite lonely as the only ageless character. Maybe you should
1045
01:08:53.159 --> 01:08:53.960
join them.
1046
01:08:54.640 --> 01:08:59.039
Wow, that's good. That's good. Uh, but uh, how about
1047
01:08:59.119 --> 01:09:00.079
if we killed you?
1048
01:09:01.359 --> 01:09:05.399
That would not be pleasant at all? Although I am
1049
01:09:05.520 --> 01:09:08.039
so busy of late, I could use the rest.
1050
01:09:09.560 --> 01:09:10.520
Ah. Good.
1051
01:09:10.680 --> 01:09:14.159
At least we could freeze you. Okay, we can keep
1052
01:09:14.239 --> 01:09:15.680
you frozen forever.
1053
01:09:16.520 --> 01:09:18.119
That would be quite peaceful.
1054
01:09:19.119 --> 01:09:21.680
But I think you like more the hit than the cold.
1055
01:09:21.720 --> 01:09:22.600
What do you like more?
1056
01:09:23.399 --> 01:09:25.920
The cold is quite fine. These bonds don't care.
1057
01:09:27.840 --> 01:09:32.000
Okay, Before we sacrifice death, is there a question from
1058
01:09:32.039 --> 01:09:33.520
the public to death?
1059
01:09:35.720 --> 01:09:35.760
No?
1060
01:09:39.000 --> 01:09:41.399
I like that, that's a good question. What is your
1061
01:09:41.479 --> 01:09:41.960
last male?
1062
01:09:42.560 --> 01:09:43.840
I prefer souls?
1063
01:09:45.279 --> 01:09:52.359
Okay, we have a question here also ruddy No, okay,
1064
01:09:52.640 --> 01:09:56.079
So why don't you come in front death here and
1065
01:09:56.159 --> 01:09:57.760
see how we can sacrifice you?
1066
01:10:02.319 --> 01:10:06.640
So I grab that we are all going to punch
1067
01:10:06.720 --> 01:10:07.960
him Halloween.
1068
01:10:09.159 --> 01:10:09.680
Halloween.
1069
01:10:10.399 --> 01:10:14.520
So yeah, we.
1070
01:10:14.479 --> 01:10:17.439
Are here to kill death before death kills us. So
1071
01:10:18.000 --> 01:10:30.800
for immortality, Viva Revolution, Viva. Okay, now, Death you can go,
1072
01:10:33.319 --> 01:10:36.920
and let's go for the questions. How we want people?
1073
01:10:37.159 --> 01:10:40.760
This is a fantastic panel. We have incredible people working
1074
01:10:40.800 --> 01:10:43.880
on different projects. I'm so excited to be here. This
1075
01:10:43.920 --> 01:10:50.800
is our family. So questions from our family members, Okay,
1076
01:10:50.920 --> 01:10:53.199
all the way, Okay, first one that is closer.
1077
01:10:54.079 --> 01:10:56.000
This is a This is more of a just an observation.
1078
01:10:57.039 --> 01:11:00.680
I thought the points you made, Joe were just truly
1079
01:11:00.720 --> 01:11:04.760
deep and profound and hit me in my heart. I
1080
01:11:04.840 --> 01:11:08.640
think all of us struggle with various things and including
1081
01:11:09.560 --> 01:11:12.680
lack of influence and frustration and ego and all that.
1082
01:11:13.399 --> 01:11:20.039
But if we can collaborate and basically put our private
1083
01:11:20.119 --> 01:11:24.720
concerns aside and think bigger and think real, longer range,
1084
01:11:24.960 --> 01:11:25.920
we'll all be better off.
1085
01:11:25.960 --> 01:11:26.760
So thank you for that.
1086
01:11:27.159 --> 01:11:32.159
Yeah, we're I mean a lot of people in this room,
1087
01:11:32.199 --> 01:11:34.720
a lot of people. The people who put rat Fest
1088
01:11:34.800 --> 01:11:38.520
together are from people unlimited and and we sort of
1089
01:11:38.520 --> 01:11:41.119
have we have the strength and the focus to do
1090
01:11:41.199 --> 01:11:43.680
that because we have we have one another.
1091
01:11:43.960 --> 01:11:46.359
Okay, so we're not working. We're not solo agents.
1092
01:11:46.640 --> 01:11:49.640
It's it's tough to be a solo agent immortalist in
1093
01:11:49.920 --> 01:11:50.880
you know, in this world.
1094
01:11:52.279 --> 01:11:54.319
Okay, we have a question here in the bank.
1095
01:11:55.840 --> 01:11:56.479
Thank you, Jove.
1096
01:11:57.000 --> 01:12:00.920
He's very inspiring to hear you all the time. Understanding
1097
01:12:01.239 --> 01:12:08.880
human being unbelievable. I treasure you. You talked recently about
1098
01:12:09.439 --> 01:12:12.239
he's going to need a new faith. That touched me
1099
01:12:12.560 --> 01:12:17.239
very deeply. Can you explain a little bit to the audience, Well,
1100
01:12:17.319 --> 01:12:19.119
you mean by having this new faith.
1101
01:12:19.199 --> 01:12:21.680
Yeah, I think I think, Uh, a lot of us
1102
01:12:22.079 --> 01:12:24.840
have felt like, oh, something was gonna happen, there's gonna
1103
01:12:24.840 --> 01:12:31.520
be a particular breakthrough before now, and have gotten discouraged.
1104
01:12:32.079 --> 01:12:35.279
Horrible things happened. I lost Bernie. I mean, that's the
1105
01:12:35.319 --> 01:12:36.680
fucking worst thing that can happen.
1106
01:12:38.600 --> 01:12:41.159
And and uh, and.
1107
01:12:41.159 --> 01:12:44.239
So these there's a faith that's basically we're externalizing.
1108
01:12:45.039 --> 01:12:45.319
Uh.
1109
01:12:45.359 --> 01:12:46.680
And this is the faith we learn it.
1110
01:12:46.720 --> 01:12:49.359
We actually learned this from religion, which is really we're
1111
01:12:49.399 --> 01:12:50.920
like and I mean to.
1112
01:12:52.439 --> 01:12:52.760
We do.
1113
01:12:53.439 --> 01:12:55.840
But but even if even if you're keep your religion,
1114
01:12:55.880 --> 01:12:59.159
we're we have we have to modify. Okay, we have to.
1115
01:12:59.239 --> 01:13:02.079
We have to develop here. And and so there's a
1116
01:13:02.119 --> 01:13:04.880
faith that's innate. It's innate to the human body. It's
1117
01:13:04.920 --> 01:13:08.079
a feeling of it's a feeling, a core gut feeling
1118
01:13:08.319 --> 01:13:11.000
of life. It's not really it's not really dependent on
1119
01:13:11.039 --> 01:13:13.960
what's happening out here. It's not really dependent on is
1120
01:13:14.000 --> 01:13:16.840
this breakthrough gonna happen, Is this piece of funding gonna happen?
1121
01:13:17.079 --> 01:13:19.640
It's it is what is It's not faith that's just
1122
01:13:19.760 --> 01:13:22.880
core in our bodies. That is it's not part of
1123
01:13:22.880 --> 01:13:25.439
our mentality. We're not really, we can't really measure it.
1124
01:13:25.640 --> 01:13:28.560
We're not really, we're not. It's not dependent on anything
1125
01:13:29.079 --> 01:13:32.000
out here, because good things happen and bad things happen.
1126
01:13:32.560 --> 01:13:36.000
And that's how we keep going because we just because it,
1127
01:13:36.199 --> 01:13:39.640
because it's it's something physical, it's something I wish Rose
1128
01:13:39.680 --> 01:13:41.600
was here. Michael Rose, you probably have something to say
1129
01:13:41.600 --> 01:13:44.520
about it, because it's something innate to the human form
1130
01:13:44.680 --> 01:13:47.760
that we're tapping into. That isn't it's not doctrinaire, it's
1131
01:13:47.840
--> 01:13:48.560
just organic.
1132
01:13:52.159 --> 01:13:52.560
Okay.
1133
01:13:52.640 --> 01:13:56.159
We have balloons for the people with questions. Uh it
1134
01:13:56.279 --> 01:13:59.960
says a stop agent in Spanish, stop and be simeon.
1135
01:14:00.439 --> 01:14:03.880
So you have a question or you one double or both?
1136
01:14:07.119 --> 01:14:10.840
What can we do? What can we do to.
1137
01:14:12.399 --> 01:14:17.000
Double this attendance of Bradfest this year, double it again
1138
01:14:17.079 --> 01:14:20.479
next year, double again, keep doubling it every year.
1139
01:14:22.840 --> 01:14:27.359
Yes, thank you. We need help. We need we need help.
1140
01:14:27.359 --> 01:14:29.159
We work our asses off. We have some We have
1141
01:14:29.159 --> 01:14:31.079
about seven hudred registrations here. It's a little bit more
1142
01:14:31.119 --> 01:14:34.319
than last year, which is which is nice. But but
1143
01:14:34.319 --> 01:14:36.199
but that's really what we want to do. That really
1144
01:14:36.279 --> 01:14:40.640
is our vision and and and we need help, like
1145
01:14:40.680 --> 01:14:44.800
we need we need other organizations to to see this
1146
01:14:45.000 --> 01:14:49.159
vision and and and share this share this opportunity with us,
1147
01:14:49.279 --> 01:14:50.800
and we need people to do it. We need people
1148
01:14:50.800 --> 01:14:52.720
to bring people and we say this every year and
1149
01:14:52.720 --> 01:14:56.279
and and the truth is it doesn't happen. So so
1150
01:14:56.279 --> 01:14:58.680
so we just shift in mindset. And I mean part
1151
01:14:58.680 --> 01:15:00.319
of it is just me being more direct, like I
1152
01:15:00.359 --> 01:15:02.800
am here. I don't think we've been this direct, but.
1153
01:15:03.800 --> 01:15:05.439
We need help. You know, people come up to us
1154
01:15:05.439 --> 01:15:06.720
and we're gonna help, We're gonna do it.
1155
01:15:06.760 --> 01:15:09.079
And a lot of times they're marketers and they're just
1156
01:15:09.119 --> 01:15:11.680
selling us their services. That's not really what I'm talking about.
1157
01:15:11.840 --> 01:15:14.720
I'm talking about like, I'm talking about people who want
1158
01:15:14.760 --> 01:15:18.000
to who want to share this vision and this mission
1159
01:15:18.039 --> 01:15:21.119
with us. Yeah, because it's for everybody.
1160
01:15:20.720 --> 01:15:24.079
Actually, Okay, okay, here another question in the front.
1161
01:15:24.800 --> 01:15:29.039
Yes, So this room is full of change agents.
1162
01:15:29.600 --> 01:15:29.840
Right.
1163
01:15:31.159 --> 01:15:35.399
When I work to create the Health Spent Action Coalition,
1164
01:15:36.119 --> 01:15:40.840
which as two hundred and seventy five cross sector organizations,
1165
01:15:41.319 --> 01:15:46.000
I worked with a wonderful operator that helped manage Props
1166
01:15:46.039 --> 01:15:49.479
seventy one and Prop fourteen and got fifteen billion dollars
1167
01:15:49.520 --> 01:15:54.199
of California taxpayer money for an agency for regenerative medicine.
1168
01:15:54.760 --> 01:15:59.479
That was the work of advocates, and that was the
1169
01:15:59.520 --> 01:16:05.720
work of narratives of people, right, narratives of people. So
1170
01:16:05.880 --> 01:16:08.600
before I took this on as a stem cell advocate,
1171
01:16:08.600 --> 01:16:12.560
in the background in law, a person that inspired me
1172
01:16:13.319 --> 01:16:18.079
was a young woman, Sabrina Cohen. She became a quadriplegic
1173
01:16:18.119 --> 01:16:21.199
and an accident when fourteen years old from Miami Beach.
1174
01:16:21.239 --> 01:16:24.119
I met her at the Miami Project to Cure Paralysis
1175
01:16:24.159 --> 01:16:26.960
when I was giving a talk. She looked just like
1176
01:16:27.079 --> 01:16:31.359
Sandra Bullock in a wheelchair. She became the first associate
1177
01:16:31.439 --> 01:16:35.399
director of my organization, a nonprofit organization that created the
1178
01:16:35.399 --> 01:16:40.000
World stem Cell Summit, and before we launched the health
1179
01:16:40.039 --> 01:16:44.560
Span Action Coalition, which was founded on an idea between
1180
01:16:44.600 --> 01:16:48.159
Aubrey and I to bring this world together. Health span
1181
01:16:48.279 --> 01:16:52.720
should be a fundamental human right. I asked Sabrina, who
1182
01:16:52.760 --> 01:16:57.119
has gone on in a top realtor and created Sabrina
1183
01:16:57.159 --> 01:17:03.520
Cohen Foundation Adaptive Beach Days in Miami. Each Sabrina does immortality.
1184
01:17:03.680 --> 01:17:08.279
Does a long life, a long lifespan matter to people
1185
01:17:08.399 --> 01:17:15.520
in your community, meaning the sci spinal cord injury community. Yes, Bernie,
1186
01:17:15.800 --> 01:17:20.399
we in our community know we're aging faster, We know
1187
01:17:20.640 --> 01:17:23.359
we are going to die young for all the things
1188
01:17:23.359 --> 01:17:26.600
that we go through day by day. And I will
1189
01:17:26.760 --> 01:17:30.800
join you and the spinal cord injury world will do
1190
01:17:30.880 --> 01:17:34.560
it be a part of this. This is cross sector
1191
01:17:35.159 --> 01:17:38.760
and it's and you are the spark. I mean, I
1192
01:17:38.800 --> 01:17:41.560
am really inspired by being here. I was nervous about
1193
01:17:41.560 --> 01:17:44.359
coming to this because I heard about Ratfest and it
1194
01:17:44.439 --> 01:17:47.079
might be like a rave and you know grave, you know,
1195
01:17:47.439 --> 01:17:49.680
but this is really the real deal. So I just
1196
01:17:49.720 --> 01:17:53.439
want to say how inspired I am and proud to
1197
01:17:53.479 --> 01:17:54.640
be associated with.
1198
01:17:54.600 --> 01:18:01.920
You and Barney those words coming from you are very
1199
01:18:02.000 --> 01:18:04.439
important to all of us, huh and all you have
1200
01:18:04.560 --> 01:18:05.680
been doing for so long.
1201
01:18:06.239 --> 01:18:10.399
So okay, yes, First of
all, Bernie, I'd like to
1202
01:18:10.760 --> 01:18:14.680
thank you for the heroic work that you and Melissa
1203
01:18:14.800 --> 01:18:19.359
King have done over the decades and advocating for stem
1204
01:18:19.439 --> 01:18:24.640
cell research, which is a crucial pathway toward life extension
1205
01:18:25.079 --> 01:18:28.640
and curing deadly diseases that could kill people in the meantime.
1206
01:18:29.039 --> 01:18:32.920
And I also wanted to echo what you said in
1207
01:18:33.000 --> 01:18:38.319
terms of encouraging people to find initiatives that already exist
1208
01:18:38.479 --> 01:18:41.760
that they could contribute to And this also goes along
1209
01:18:41.760 --> 01:18:47.039
the lines of what Joe articulated, because even when I
1210
01:18:47.079 --> 01:18:49.319
was looking out to see how I could contribute to
1211
01:18:49.359 --> 01:18:52.960
the field, I was thinking about what endeavors were already
1212
01:18:53.079 --> 01:18:57.960
in progress that needed help. And you are important, as
1213
01:18:58.039 --> 01:19:01.439
Joe said, one person can make a difference within that
1214
01:19:01.560 --> 01:19:05.479
collaborative approach. Like with led the game, I saw that
1215
01:19:05.520 --> 01:19:08.439
there was a previous team that had tried to develop
1216
01:19:08.479 --> 01:19:11.079
it but didn't have the funds, and I didn't want
1217
01:19:11.079 --> 01:19:13.479
that project to just languish. I didn't want it to
1218
01:19:13.560 --> 01:19:16.880
disappear down the memory hole, since there wasn't even the
1219
01:19:16.920 --> 01:19:20.479
source code for the original game remaining. So I brought
1220
01:19:20.479 --> 01:19:23.760
it to a playable state. But I needed another individual
1221
01:19:23.840 --> 01:19:26.840
Y'ari starin Vukotich to program it. I needed the community
1222
01:19:26.880 --> 01:19:31.600
to provide feedback. Likewise with the Transhumanist Party, when Zoltenischwan
1223
01:19:31.920 --> 01:19:34.920
founded it, he ran for president. He had the Immortality
1224
01:19:34.920 --> 01:19:39.119
Bus campaign. In twenty sixteen, he decided he wanted to
1225
01:19:39.159 --> 01:19:42.119
move on to other endeavors, so he stepped down from
1226
01:19:42.119 --> 01:19:45.159
the leadership role of the Transhumanist Party. Really, he's more
1227
01:19:45.239 --> 01:19:49.279
like a serial startup founder than someone who keeps an
1228
01:19:49.319 --> 01:19:52.239
initiative going for years, but he wanted it to go
1229
01:19:52.319 --> 01:19:55.479
on for years. He wanted it to outlast his tenure.
1230
01:19:55.560 --> 01:19:58.600
So he asked me to be the chairman, and I decided, well,
1231
01:19:58.840 --> 01:20:02.680
this is my opportunity to contribute to something longer lasting
1232
01:20:02.720 --> 01:20:05.199
and perhaps something that would last beyond my own tenure
1233
01:20:05.479 --> 01:20:08.600
as chairman. So think about those kinds of initiatives, those
1234
01:20:08.640 --> 01:20:11.239
that are already in progress that you could make a
1235
01:20:11.279 --> 01:20:13.680
difference and you could carry to the next level.
1236
01:20:15.520 --> 01:20:18.960
Okay, good point, eleanor a balloon, I'm a question.
1237
01:20:19.640 --> 01:20:22.760
I want I want to ask the question for the balloon,
1238
01:20:22.840 --> 01:20:25.920
So thank you so much. No, but so you were talking,
1239
01:20:26.000 --> 01:20:31.800
Joe about numbers matter and which is true, but there's
1240
01:20:31.800 --> 01:20:36.159
something about passion and having such a conviction of moving
1241
01:20:36.199 --> 01:20:39.000
this initiative forward, and I was wondering, if you this
1242
01:20:39.039 --> 01:20:41.800
is a good time maybe to tell all these activists
1243
01:20:41.840 --> 01:20:46.199
here what it takes to create Radfist and how even
1244
01:20:46.479 --> 01:20:48.880
one more person that jumps in in the way that
1245
01:20:48.920 --> 01:20:51.840
they can contribute can make a difference, because I don't
1246
01:20:51.880 --> 01:20:54.960
know if people here know what kind of team you
1247
01:20:55.000 --> 01:20:59.560
guys have and how long it takes to actually produce
1248
01:20:59.640 --> 01:21:01.840
this of So maybe you can give a little bit
1249
01:21:01.840 --> 01:21:02.720
of detail.
1250
01:21:03.079 --> 01:21:08.840
Yeah, we have a really small, really good team. Uh
1251
01:21:09.319 --> 01:21:12.399
of I want to say, you know, Michelle Andrews uh,
1252
01:21:12.760 --> 01:21:19.119
Jeene Wideman, uh, Marianna Cellis and Daniella Escobar is the
1253
01:21:19.159 --> 01:21:23.000
team with Jim and I and you know they're working
1254
01:21:23.039 --> 01:21:27.039
on that, uh you know, most of the year, most
1255
01:21:27.079 --> 01:21:34.680
of the year and so so. But but the vision
1256
01:21:34.720 --> 01:21:38.079
is of a platform, and that's and that's where we
1257
01:21:38.119 --> 01:21:41.960
can do something that doesn't really have a limit in
1258
01:21:42.079 --> 01:21:45.960
size and and we basically do it on like a
1259
01:21:46.079 --> 01:21:51.479
zero budget. Like we basically do it on on uh
1260
01:21:51.760 --> 01:21:55.199
there's there's no extra money in this, so we you know,
1261
01:21:55.800 --> 01:21:58.359
and and Jim doesn't get paid, you know, and I
1262
01:21:58.359 --> 01:21:59.279
get paid a little bit.
1263
01:21:59.600 --> 01:21:59.800
You know.
1264
01:22:00.039 --> 01:22:03.479
That's why I'm doing uh uh messaging strategy for you know,
1265
01:22:03.520 --> 01:22:06.199
boring companies, but which I try to help them.
1266
01:22:06.279 --> 01:22:09.439
But yeah, so so.
1267
01:22:11.720 --> 01:22:13.199
And this is a little bit, this is a little
1268
01:22:13.199 --> 01:22:15.399
bit where we are because because we're on the cutting
1269
01:22:15.479 --> 01:22:18.159
edge of longevity, right, I mean that's and and this
1270
01:22:18.239 --> 01:22:21.319
is where this is where the space is
right now
1271
01:22:21.520 --> 01:22:24.159
and it doesn't need to be like we could have
1272
01:22:24.359 --> 01:22:29.239
we could have volunteers that have superb capability that could really,
1273
01:22:29.359 --> 01:22:32.600
as you're saying, really expand what we're doing. We could
1274
01:22:32.640 --> 01:22:34.199
have a chunk of money that isn't even that big
1275
01:22:34.199 --> 01:22:36.760
of a chunk of money that could change how we
1276
01:22:36.800 --> 01:22:42.199
function so so and it's time for that. Honestly, it's
1277
01:22:42.239 --> 01:22:44.479
time for that. So you guys love rat Fest. We
1278
01:22:44.520 --> 01:22:48.439
love rat Fest, but you know we don't honestly, we
1279
01:22:48.439 --> 01:22:49.880
don't want to keep just doing it like this.
1280
01:22:50.880 --> 01:22:51.319
We don't.
1281
01:22:51.439 --> 01:22:54.720
We we we we we want it. We have to
1282
01:22:54.760 --> 01:22:58.920
go uh in a more. I want to say bigger,
1283
01:22:58.960 --> 01:23:00.880
but it's not just about bigger. It's it's just an
1284
01:23:00.880 --> 01:23:04.439
ex we have to expand. That's that's, that's what has
1285
01:23:04.479 --> 01:23:04.880
to happen.
1286
01:23:05.399 --> 01:23:09.399
I add that one person with a passion is more
1287
01:23:09.479 --> 01:23:12.760
powerful than one hundred people with an interest. So whatever
1288
01:23:12.800 --> 01:23:15.880
we can do to increase passion in ourselves, we need
1289
01:23:15.920 --> 01:23:17.680
to do that. And we need to bring more people
1290
01:23:17.760 --> 01:23:20.319
in who have passion more so than interest.
1291
01:23:23.399 --> 01:23:28.199
Yeah, just let me add we need to collaborate internationally.
1292
01:23:28.600 --> 01:23:30.960
Like for example, I'm very happy that every year I
1293
01:23:31.039 --> 01:23:34.680
bring friends. In fact, here is a Spanish friend Elena,
1294
01:23:35.319 --> 01:23:39.199
and there is as a Mexican friend Dorris, and then
1295
01:23:39.399 --> 01:23:40.279
also Cody.
1296
01:23:40.920 --> 01:23:42.279
Cody always brings friends.
1297
01:23:42.319 --> 01:23:46.319
We have Mark Hamilton, we have well as behind all
1298
01:23:46.359 --> 01:23:47.279
of us bring people.
1299
01:23:47.319 --> 01:23:48.479
We need to bring more people.
1300
01:23:48.520 --> 01:23:51.119
We need to collaborate, and we need to keep this
1301
01:23:51.520 --> 01:23:56.159
growing growing, and also in different places. Because I organize
1302
01:23:56.199 --> 01:23:59.840
something in Spain as well. On my public is mostly
1303
01:24:00.000 --> 01:24:03.000
Spanish and then some of those come here as well.
1304
01:24:03.560 --> 01:24:07.359
So we need to keep on collaborating and also experiment
1305
01:24:07.439 --> 01:24:11.800
different things like we are doing this march in the
1306
01:24:11.880 --> 01:24:14.439
Centers of Power of Spain. That is why I think
1307
01:24:14.479 --> 01:24:17.000
it's so important that we have a rally for Longevity
1308
01:24:17.000 --> 01:24:17.840
in Washington, d C.
1309
01:24:18.520 --> 01:24:20.239
Washington d C has to see this.
1310
01:24:20.880 --> 01:24:27.279
As Gennadi mentioned the Immortality Bones the coffin, it was
1311
01:24:27.279 --> 01:24:31.359
a coffin in front of the US Capitol that actually
1312
01:24:31.359 --> 01:24:35.239
should have had more media coverage. And you know, the
1313
01:24:35.359 --> 01:24:39.520
Coalition for Radical Eve Extension can do it and better
1314
01:24:40.079 --> 01:24:45.199
because I like Sultan Isban, but it was one man show.
1315
01:24:45.840 --> 01:24:49.279
Here we are hundreds of people from all over the world.
1316
01:24:49.760 --> 01:24:53.600
And then before giving you the word gym, because there
1317
01:24:53.600 --> 01:24:55.479
are other initiatives we need to adapt.
1318
01:24:55.640 --> 01:24:56.479
And I want.
1319
01:24:56.279 --> 01:25:00.640
To ask, because Cody hasn't spoken too much, where we
1320
01:25:00.680 --> 01:25:03.199
are going to be next month and what we are
1321
01:25:03.239 --> 01:25:04.359
going to do next month.
1322
01:25:05.239 --> 01:25:07.359
Yeah, let me let me just jump in just quickly. Look,
1323
01:25:10.119 --> 01:25:16.079
we're not just like immortality entrepreneurs. We're not just like
1324
01:25:16.560 --> 01:25:19.600
starting something and moving on to the next thing.
1325
01:25:20.039 --> 01:25:22.840
That's not what we're doing. We're we're we're.
1326
01:25:22.520 --> 01:25:24.680
In this and we're not going to quit on this,
1327
01:25:24.760 --> 01:25:26.439
and we're actually not going to quit on you.
1328
01:25:26.960 --> 01:25:28.560
And that's the difference. You know.
1329
01:25:29.520 --> 01:25:31.840
It's it's one thing to have a campaign and do
1330
01:25:31.920 --> 01:25:34.680
something and then disappear into something else. That's not what
1331
01:25:34.840 --> 01:25:37.760
That's not what we're about. We're we're on this and
1332
01:25:37.800 --> 01:25:40.079
I and we've shown that because ten years is ten years.
1333
01:25:40.239 --> 01:25:43.720
We're we're we're on this to stay. That's that's why, honestly,
1334
01:25:43.760 --> 01:25:44.960
that's why you should support us.
1335
01:25:45.319 --> 01:25:48.199
Well, we are here to kill death. Look at it
1336
01:25:48.399 --> 01:25:50.800
death there. We are here to kill you.
1337
01:25:51.720 --> 01:25:52.000
Uh.
1338
01:25:52.039 --> 01:25:55.000
And there are different approaches. So so what are we
1339
01:25:55.079 --> 01:25:57.359
going to do? Who are we going to meet where?
1340
01:25:57.399 --> 01:25:57.760
Cody?
1341
01:25:58.119 --> 01:26:01.680
Okay, Well, first I wanted to say, Immortalis is kind
1342
01:26:01.680 --> 01:26:05.039
of doing slightly what Radfast is doing, but on a
1343
01:26:05.039 --> 01:26:08.840
different stage. So Radfest gives the scientists and the researchers
1344
01:26:08.840 --> 01:26:12.359
of longevity the stage and the voice to the public
1345
01:26:12.720 --> 01:26:16.039
and immortalis is giving the stage to those same people
1346
01:26:16.399 --> 01:26:20.760
to move forward faster and what they're doing. So next
1347
01:26:20.840 --> 01:26:23.520
month we are going with jose To. He's going to
1348
01:26:23.600 --> 01:26:27.159
introduce us to one of his friends in Argentina, Javier Malay.
1349
01:26:27.199 --> 01:26:30.239
The President of Argentina, is going to meet with us
1350
01:26:30.720 --> 01:26:35.279
with Mark Wallas, I mean Mark Hamilton Wallas and Cody
1351
01:26:35.359 --> 01:26:40.239
and myself because we are proposing to have Immortalists in
1352
01:26:40.560 --> 01:26:44.119
Buenos Aires, south of Buenos Aires, and we want competition.
1353
01:26:44.359 --> 01:26:46.640
Also the USA has to get in there. Of course,
1354
01:26:46.680 --> 01:26:47.920
the USA has to be there.
1355
01:26:48.359 --> 01:26:51.520
Argentina is one of three or four governments we're in
1356
01:26:51.560 --> 01:26:52.520
talks with right now.
1357
01:26:54.359 --> 01:26:59.079
So okay, Jim here is the father of the beast.
1358
01:27:00.359 --> 01:27:01.079
Thank you. I'll thank you.
1359
01:27:01.119 --> 01:27:03.119
A great job. You guys, great John, thank you, thank
1360
01:27:03.119 --> 01:27:05.720
you all of it. You're great, You're fantastic. I just
1361
01:27:05.720 --> 01:27:08.079
want to make one thing simple here that I'm feeling
1362
01:27:08.079 --> 01:27:10.359
about all this and uh oh oh, you guys look great,
1363
01:27:10.359 --> 01:27:13.039
by the way, is that I want to keep it
1364
01:27:13.079 --> 01:27:15.439
simple in the context that when we talk about companies
1365
01:27:15.439 --> 01:27:19.079
and everything, uh, you know, helping and expanding and helping
1366
01:27:19.079 --> 01:27:21.680
and expand you don't have we're not talking about anybody
1367
01:27:21.720 --> 01:27:23.880
stopping what you're doing. What you're doing is great, what
1368
01:27:24.000 --> 01:27:27.399
your cody, all you guys Janati, But but make Radfest
1369
01:27:27.439 --> 01:27:30.600
your home and the context that make it your base. Uh,
1370
01:27:30.680 --> 01:27:33.279
make it. Make it that you're telling your people, all
1371
01:27:33.319 --> 01:27:36.439
your members from the big right when Radfest ends, that
1372
01:27:36.520 --> 01:27:39.239
they need to be at Radfest, not just sitting back
1373
01:27:39.279 --> 01:27:42.000
and waiting for you know, your different meetings you have,
1374
01:27:42.079 --> 01:27:44.199
get them, get them, You're already doing that in some state.
1375
01:27:44.359 --> 01:27:45.880
But this is really what we're talking about. This is
1376
01:27:45.880 --> 01:27:48.039
the simplicity of it. This is how we're going to double.
1377
01:27:48.159 --> 01:27:50.760
This is how we're going to triple. In fact, everybody
1378
01:27:50.800 --> 01:27:53.720
here talking to your friends, your family, everybody, get into
1379
01:27:53.760 --> 01:27:56.960
this
conversation, get into this life speaking, speak it up
1380
01:27:57.199 --> 01:27:59.720
and making it that simple. Uh, you know, we're we're
1381
01:27:59.760 --> 01:28:01.960
we're come many. Thank you Joe for your presentation. All
1382
01:28:02.039 --> 01:28:04.920
you guys, like I said, you're amazing. But let's keep
1383
01:28:04.920 --> 01:28:07.720
it also to this point simple that we talked to
1384
01:28:07.800 --> 01:28:10.800
our people right when you're right, when Radfest ends, you're
1385
01:28:11.279 --> 01:28:13.520
setting them up, and you do a great job setting
1386
01:28:13.560 --> 01:28:16.199
them up now to be here and it will be
1387
01:28:16.239 --> 01:28:18.479
this then Radfest will build something that will be a
1388
01:28:18.479 --> 01:28:19.560
springboard for all of us.
1389
01:28:19.600 --> 01:28:20.800
It will build everybody.
1390
01:28:21.159 --> 01:28:24.520
That's the point. By us focusing together and this initiative,
1391
01:28:24.560 --> 01:28:27.359
we will build then everybody's initiative along with that. But
1392
01:28:27.399 --> 01:28:29.520
if we don't have that one focus, we're scattered, and
1393
01:28:29.560 --> 01:28:30.359
that's what happens.
1394
01:28:30.680 --> 01:28:38.079
Thank you, Uh one, two and three.
1395
01:28:39.600 --> 01:28:42.319
Yes, My wife is the president of our vice president
1396
01:28:42.359 --> 01:28:47.199
of ALICE, which is the Latin American Sociology Association. They
1397
01:28:47.239 --> 01:28:51.800
have their conferences every two years. So what they do
1398
01:28:51.840 --> 01:28:55.600
in the meantime is they have pre ALICE conferences all
1399
01:28:55.640 --> 01:28:58.479
over Latin America. There might be three or four or
1400
01:28:58.479 --> 01:29:02.359
five of them in Mexico alone, And optimally you want
1401
01:29:02.399 --> 01:29:05.279
those people coming to your main conference, but in truth,
1402
01:29:05.279 --> 01:29:06.680
they're not all going to go there. So what would
1403
01:29:06.720 --> 01:29:09.399
happen is you would invite just a few speakers from
1404
01:29:09.399 --> 01:29:11.920
the main conference to go to all these different locations
1405
01:29:12.199 --> 01:29:15.520
you're promoting it. My wife's the president of ten universities
1406
01:29:15.560 --> 01:29:18.720
in Mexico. We would hold one our university that would
1407
01:29:18.760 --> 01:29:21.000
give us, and we make it very an expensive for
1408
01:29:21.000 --> 01:29:23.760
the students to come. So the students, you know, pay
1409
01:29:23.800 --> 01:29:27.079
the expenses of the conference, and most of those you know,
1410
01:29:27.640 --> 01:29:30.000
ninety percent of those students and other people don't go
1411
01:29:30.039 --> 01:29:31.960
to the main conference, but you're still spreading the word.
1412
01:29:37.760 --> 01:29:42.199
Okay, so I don't even know where to start. To
1413
01:29:42.279 --> 01:29:46.640
your point, what I tell my friends, just to simplify,
1414
01:29:46.920 --> 01:29:50.800
is I'm going to the first largest conference in the
1415
01:29:50.840 --> 01:29:58.920
world on longevity. Your presentation was right on. I'm a
1416
01:29:58.960 --> 01:30:03.439
global marketing comunication expert and I'm not selling anything. I
1417
01:30:03.479 --> 01:30:06.479
want to collaborate and help. I told lis Perish that
1418
01:30:06.960 --> 01:30:11.119
I moved to Mexico because I believe that access to
1419
01:30:11.960 --> 01:30:16.880
the things that people need are much easier being in Mexico.
1420
01:30:17.279 --> 01:30:23.560
I speak Spanish, so unfortunate. So whatever is needed, I'm there.
1421
01:30:24.039 --> 01:30:25.039
I'm in Tijuana.
1422
01:30:25.319 --> 01:30:26.399
I'm right on the border.
1423
01:30:27.600 --> 01:30:31.279
One of the things that I think is critical in
1424
01:30:31.359 --> 01:30:36.560
my opinion of teaching at MBA programs, working and marketing
1425
01:30:36.560 --> 01:30:39.720
all my life is you need to think from the
1426
01:30:39.760 --> 01:30:44.119
outside and versus inside out. What does that mean when
1427
01:30:44.239 --> 01:30:48.600
I talk to people, regular people? To your point, how
1428
01:30:48.640 --> 01:30:54.159
do you double attendance? You need to get people excited
1429
01:30:54.600 --> 01:30:57.720
and passionate. The people that I talk to about this
1430
01:30:57.920 --> 01:31:03.960
concept are afraid. They're afraid, and what are they afraid of?
1431
01:31:04.800 --> 01:31:09.039
You'll never guess. They're afraid of loneliness. They're like, if
1432
01:31:09.079 --> 01:31:11.760
I outlive, I look at my mother.
1433
01:31:11.960 --> 01:31:15.600
Two of her friends just died. It's very sad.
1434
01:31:16.359 --> 01:31:20.680
So when you're talking, when you're excited, because you've already
1435
01:31:20.720 --> 01:31:24.680
bought into the concept, you cannot get through people. And
1436
01:31:24.720 --> 01:31:27.359
I'll tell you this as a marketer for many years,
1437
01:31:27.720 --> 01:31:33.279
you will just people will just be negative or they'll
1438
01:31:33.399 --> 01:31:37.399
just shut down. You will not convince them in that way.
1439
01:31:38.039 --> 01:31:41.399
So what's needed is to your point, this is a
1440
01:31:41.439 --> 01:31:44.840
time for strategy. This is a time to sit down
1441
01:31:44.960 --> 01:31:48.960
and figure out all of the strategic elements of driving
1442
01:31:49.000 --> 01:31:53.640
this movement forward. One with collaboration, one with messaging, one
1443
01:31:53.720 --> 01:31:59.119
with outreach, very clear, simple messages that can help people
1444
01:31:59.239 --> 01:32:03.199
get over the fear, look at the benefits, sell them
1445
01:32:03.279 --> 01:32:07.720
on the benefits so that you can bypass either misinformation
1446
01:32:08.800 --> 01:32:12.319
or just get them thinking in a more positive way.
1447
01:32:12.760 --> 01:32:16.359
And I'm also open to helping in any way with
that.
1448
01:32:16.359 --> 01:32:19.319
That is one of my expertises as well. But I
1449
01:32:19.399 --> 01:32:22.479
believe there's so much that can be done at this moment.
1450
01:32:22.680 --> 01:32:25.439
There's a lot of momentum, but it is a time
1451
01:32:25.479 --> 01:32:30.399
to collaborate and be strategic so that you limit the
1452
01:32:30.479 --> 01:32:36.199
resources and with less energy, you can do more and it's.
1453
01:32:36.039 --> 01:32:37.600
Hard, but it's doable.
1454
01:32:37.680 --> 01:32:42.640
You have amazing people. There's amazing people here that I'm
1455
01:32:42.720 --> 01:32:45.520
just like, I've never expected to see all of this.
1456
01:32:45.880 --> 01:32:49.239
I've been in touch with Jose, I knew about all
1457
01:32:49.279 --> 01:32:52.039
of these conferences. But there's so much more that I
1458
01:32:52.079 --> 01:32:55.000
think can be done just to move all of these forwards.
1459
01:32:55.000 --> 01:32:57.880
So again, thank you for that presentation. I think it
1460
01:32:57.920 --> 01:32:58.520
was wonderful.
1461
01:32:59.359 --> 01:33:03.399
Yeah, thank you, thank you for your comments, and we'd
1462
01:33:03.399 --> 01:33:06.319
like to connect more with you. I do want to
1463
01:33:06.399 --> 01:33:09.720
say that the more obvious opportunity is people who are
1464
01:33:09.760 --> 01:33:13.159
already into longevity. Okay, we're talking about travel, We're talking
1465
01:33:13.159 --> 01:33:15.560
about paying a registration fee, We're talking about spending a
1466
01:33:15.560 --> 01:33:19.079
couple of days somewhere. That's the obvious target. It is
1467
01:33:19.279 --> 01:33:24.119
It is the transhumanists. Okay, there's like this, there's there's
1468
01:33:24.239 --> 01:33:28.159
actually a significant number of transhumanists. There's actually a significant
1469
01:33:28.239 --> 01:33:31.119
number of longevity people. I'm not saying we shouldn't reach
1470
01:33:31.119 --> 01:33:33.039
out expand the market. We one hundred percent want to
1471
01:33:33.119 --> 01:33:36.079
do that, but let's mobilize the people who are already
1472
01:33:36.439 --> 01:33:39.600
into this to actually, you know, fucking do something.
1473
01:33:44.399 --> 01:33:45.199
I have some.
1474
01:33:45.680 --> 01:33:49.039
Feedback that might help us improve our message. There's an
1475
01:33:49.159 --> 01:33:53.520
organization called this Stage. It's an international organization of forty
1476
01:33:53.520 --> 01:33:57.439
five thousand CEOs and thirty seven countries. I'm a speaker
1477
01:33:57.479 --> 01:34:01.479
to them on sales and also longevity. My astartmental longevity
1478
01:34:01.520 --> 01:34:04.760
presentation will ask raise your hand if you would like
1479
01:34:04.840 --> 01:34:10.159
to live forever. About half raise their hand. Then I'll say, okay,
1480
01:34:10.239 --> 01:34:12.000
raise your hand if you'd like to live forever with
1481
01:34:12.039 --> 01:34:16.159
great health, a sharp mind, unhitted mobility. Now we're at
1482
01:34:16.159 --> 01:34:19.479
three quarters. And then if I ask, raise your hand
1483
01:34:19.560 --> 01:34:23.720
if you and your family and your friends could live
1484
01:34:23.760 --> 01:34:28.239
forever with great hell, almost everybody raises their hands. So
1485
01:34:28.319 --> 01:34:31.279
we might think about that and somehow it might help
1486
01:34:31.359 --> 01:34:35.560
us improve the message. The second of feedback I get
1487
01:34:35.600 --> 01:34:40.880
this negative is this is against God's will. God has
1488
01:34:40.960 --> 01:34:43.279
determined how long we're gonna live, and there's nothing we
1489
01:34:43.319 --> 01:34:46.039
can do about it. So there's no need for me
1490
01:34:46.079 --> 01:34:49.680
to get involved. I don't have an answer for that myself. Well,
1491
01:34:49.760 --> 01:34:52.279
I will tell you my wife's Catholic and that's how
1492
01:34:52.319 --> 01:34:56.760
she feels. So there's two philosophies of life determinism. So
1493
01:34:56.800 --> 01:34:59.840
I just mentioned that she believes in and the others
1494
01:35:00.079 --> 01:35:03.399
you will. That means I'm in charge of how long
1495
01:35:03.439 --> 01:35:06.920
I'm gonna live, and number one by what I do.
1496
01:35:07.039 --> 01:35:10.159
And number two, if I'm doing good for the world
1497
01:35:10.279 --> 01:35:12.880
like I think I'm trying to do, then the man
1498
01:35:12.960 --> 01:35:15.279
upstairs will see that and keep you a life longer.
1499
01:35:16.279 --> 01:35:17.880
So I just want to make sure those two main
1500
01:35:17.960 --> 01:35:20.159
pushbacks so it might help us improve our message.
1501
01:35:22.159 --> 01:35:23.279
A beautiful guess.
1502
01:35:23.159 --> 01:35:24.960
I just just a piggyback on that.
1503
01:35:25.039 --> 01:35:26.680
I do think I know I did a little bit,
1504
01:35:26.720 --> 01:35:29.000
but I do think we need to stop this like
1505
01:35:29.159 --> 01:35:34.960
boxing match with religion. Like let's let's uh yeah, yeah,
1506
01:35:35.039 --> 01:35:36.520
you know, if you believe in a god, just believe
1507
01:35:36.560 --> 01:35:37.560
in a god who wants you to live.
1508
01:35:38.680 --> 01:35:41.199
You know. Yeah, let's welcome everybody.
1509
01:35:41.560 --> 01:35:45.920
It's actually for it's actually for everybody, Yeah, because because
1510
01:35:45.960 --> 01:35:49.399
we want to live. It's not about a doctor, a doctor,
1511
01:35:49.479 --> 01:35:53.000
an agreement in doctrine. That's that's not it's not really
1512
01:35:53.000 --> 01:35:55.039
about that. It's about it's about human beings living.
1513
01:35:55.319 --> 01:35:55.520
Right.
1514
01:35:56.920 --> 01:36:03.680
Yes, So, uh, I agree with you, Joe. I think determinism,
1515
01:36:04.319 --> 01:36:08.119
irrespective of religious or philosophical roots, as a kind of
1516
01:36:08.760 --> 01:36:14.880
evolved coping mechanism that various traditions of thought have
developed
1517
01:36:14.920 --> 01:36:19.680
over the course of millennia when mortality really was unavoidable
1518
01:36:19.720 --> 01:36:23.039
because the technology just wasn't there, So people figured out
1519
01:36:23.079 --> 01:36:26.000
a way to make peace with death instead of trying
1520
01:36:26.039 --> 01:36:28.840
to fight it. The problem with that mindset is right
1521
01:36:28.880 --> 01:36:31.199
now we are on the cusp of being able to
1522
01:36:31.279 --> 01:36:34.680
kill death, but it will be dependent on our efforts.
1523
01:36:34.680 --> 01:36:40.319
So any sort of determinism or fatalism will undermine those efforts,
1524
01:36:40.399 --> 01:36:43.880
and we ultimately need the religious communities of the world
1525
01:36:43.920 --> 01:36:47.560
to align with us on this. As I've said yesterday,
1526
01:36:47.600 --> 01:36:51.479
religions evolved too, and we can hopefully influence them to
1527
01:36:51.600 --> 01:36:55.920
evolve in a positive direction without requiring people to give
1528
01:36:56.000 --> 01:36:59.279
up something that's valuable to them. So I'm an atheist,
1529
01:36:59.279 --> 01:37:01.680
but I don't want to convert anybody. If you are
1530
01:37:02.079 --> 01:37:04.279
a Christian or a Jew, or a Muslim, or a
1531
01:37:04.359 --> 01:37:06.479
Hindu or a Buddhist, I want you to be a
1532
01:37:06.560 --> 01:37:08.800
Christian or Jew, or a Muslim or Hindu or Buddhist
1533
01:37:08.800 --> 01:37:12.840
who believes in immortality or radical life extension.
1534
01:37:12.600 --> 01:37:13.319
In this world.
1535
01:37:14.560 --> 01:37:17.119
Yes, and that's that's how we can get to it together.
1536
01:37:17.159 --> 01:37:19.960
And then we could argue about theology or philosophy all
1537
01:37:19.960 --> 01:37:23.479
we want. Once we have immortality, and then we could
1538
01:37:23.479 --> 01:37:27.600
actually drill deeply into what we believe and why without
1539
01:37:27.680 --> 01:37:28.680
running out of time to do it.
1540
01:37:28.760 --> 01:37:30.479
We argue about it forever if we wanted.
1541
01:37:31.359 --> 01:37:31.439
So.
1542
01:37:31.800 --> 01:37:34.640
I don't understand the argument of it's against God's will
1543
01:37:34.680 --> 01:37:37.680
for longevity, because the Bible says we're created in God's image,
1544
01:37:37.720 --> 01:37:39.359
and I haven't heard about God dying.
1545
01:37:39.520 --> 01:37:43.239
So that's right.
1546
01:37:44.199 --> 01:37:47.199
It's the Hebrews Btseilla Melohem, right, So that's in the
1547
01:37:47.479 --> 01:37:48.960
It's in the image of God.
1548
01:37:49.319 --> 01:37:51.079
The Gospel of longevity.
1549
01:37:52.159 --> 01:37:55.439
Jim, Okay, we have a question here, Bob under balloon.
1550
01:37:56.600 --> 01:38:02.079
Yeah, I think we need to walk our I had
1551
01:38:02.119 --> 01:38:07.319
my fifty year service celebration at the Boeing Company about
1552
01:38:07.359 --> 01:38:09.640
three months ago, and it happened to be in the
1553
01:38:09.720 --> 01:38:11.680
middle of one of my fasting periods.
1554
01:38:12.039 --> 01:38:13.640
I thought, I'm not going to break my fast for this.
1555
01:38:14.079 --> 01:38:14.359
Hell.
1556
01:38:14.439 --> 01:38:19.199
No, you gotta take charge of yourself and say I'm
1557
01:38:19.199 --> 01:38:19.880
going to be different.
1558
01:38:20.159 --> 01:38:21.199
You gear are different.
1559
01:38:21.479 --> 01:38:25.439
You know, do the things and do not pay attention
1560
01:38:25.520 --> 01:38:29.279
to what the masses who follow the sheep expectation follow.
1561
01:38:29.960 --> 01:38:31.920
You're going to retire, not to death, but to do
1562
01:38:32.000 --> 01:38:38.359
more things. When you have your fifty year self fast
1563
01:38:38.359 --> 01:38:40.000
if you can fast, you know, don't stop.
1564
01:38:41.960 --> 01:38:45.920
Okay, we have time for two more questions, and also
1565
01:38:46.000 --> 01:38:48.880
remember after this we're going to have a very nice meal.
1566
01:38:49.680 --> 01:38:51.439
Life is also to be enjoyed.
1567
01:38:51.439 --> 01:38:53.920
That is why we want to be immortal, because we
1568
01:38:53.960 --> 01:38:56.920
want to have fun. We have to enjoy life, so
1569
01:38:57.560 --> 01:39:00.720
the food will be nice. But we have time for questions.
1570
01:39:00.960 --> 01:39:03.560
One question here, Taylor.
1571
01:39:04.479 --> 01:39:07.279
Yeah, I have a couple of questions. One is actually
1572
01:39:07.279 --> 01:39:12.000
for you, Jose in Madrid, are you are your speakers
1573
01:39:12.000 --> 01:39:13.880
that you have planned? Are they actually going to be
1574
01:39:13.920 --> 01:39:17.479
there in person and not over zoom because that's a
1575
01:39:17.520 --> 01:39:19.840
far away to travel for a lot of us. And
1576
01:39:19.920 --> 01:39:21.159
another is for Ganadi.
1577
01:39:21.600 --> 01:39:23.119
And we've had a lot.
1578
01:39:22.920 --> 01:39:26.000
Of exciting protocols announced here on the main stage and
1579
01:39:26.039 --> 01:39:30.359
in some of the clinics, and are you considering incorporating
1580
01:39:30.399 --> 01:39:33.920
any of those into your game, as you know things
1581
01:39:33.920 --> 01:39:36.600
that might pop up if you're advocating for anti aging.
1582
01:39:38.319 --> 01:39:41.039
Okay, the first question, yes, I like to do like
1583
01:39:41.119 --> 01:39:45.600
in Radfast, the speakers have to be there because I
1584
01:39:45.640 --> 01:39:47.640
want also the people to talk with the speakers.
1585
01:39:47.640 --> 01:39:48.439
This is important.
1586
01:39:48.720 --> 01:39:52.520
And yesterday there was a beautiful VIP reception with the
1587
01:39:52.560 --> 01:39:55.760
speakers and those participants who wanted to go, and so
1588
01:39:55.840 --> 01:39:57.000
I want them to be in touch.
1589
01:39:57.199 --> 01:39:58.560
There are certain exceptions.
1590
01:39:58.640 --> 01:40:02.359
Last year I had Brian Joe, but Brian Johnson tries
1591
01:40:02.399 --> 01:40:05.760
to avoid international trouble because of his Arcadian rhythm and
1592
01:40:05.840 --> 01:40:09.199
he's sleep and this year so he didn't come in person.
1593
01:40:09.279 --> 01:40:11.840
He was by zoom. This year I also have one
1594
01:40:11.880 --> 01:40:16.159
person byzom who is George. George Church is no longer
1595
01:40:16.199 --> 01:40:20.520
traveling internationally and so it's Ray Kersweil. He doesn't travel internationally.
1596
01:40:20.640 --> 01:40:23.600
But otherwise, all the people are coming to Madrid. Yes,
1597
01:40:23.640 --> 01:40:26.159
this is a real conference and I have tours for them.
1598
01:40:26.199 --> 01:40:29.680
I want them to enjoy life, to see how beautiful
1599
01:40:29.680 --> 01:40:33.640
life is and how fantastic the Mediterranean diet is.
1600
01:40:34.760 --> 01:40:39.319
Yes, So Taylor, to answer your question, I'm of course
1601
01:40:39.359 --> 01:40:41.920
still open to feedback on LV the game.
1602
01:40:41.920 --> 01:40:43.600
We're currently unbuild.
1603
01:40:43.479 --> 01:40:45.920
Zero point nine to one, so we're not at one
1604
01:40:45.920 --> 01:40:49.399
point zero yet. The game is open to iteration and
1605
01:40:49.640 --> 01:40:52.880
refinement now in terms of how specific do we want
1606
01:40:52.920 --> 01:40:55.960
to get. There's a reason why I had a singular
1607
01:40:56.039 --> 01:41:01.079
selection for fitness regimen and the singular selection for improve nutrition.
1608
01:41:01.199 --> 01:41:05.399
It's supposed to be whatever you think works or whatever
1609
01:41:05.520 --> 01:41:08.479
works for you or whatever ends up working in practice.
1610
01:41:08.520 --> 01:41:11.479
And the reason why I did that was because I
1611
01:41:11.520 --> 01:41:15.680
wanted to show at least the approximate scale of effects.
1612
01:41:15.760 --> 01:41:18.039
So if you engage in the.
1613
01:41:18.000 --> 01:41:21.880
Best possible fitness regimen, whatever that happens to be, that
1614
01:41:21.920 --> 01:41:25.039
could reverse your aging somewhat, that could rejuvenate you somewhat,
1615
01:41:25.079 --> 01:41:28.159
make you healthier, make you live longer. It's not going
1616
01:41:28.199 --> 01:41:30.359
to make you live to one fifty. Likewise, if you
1617
01:41:30.439 --> 01:41:33.119
have the best diet in the world, it could help
1618
01:41:33.159 --> 01:41:35.640
you live longer, it could help you avoid certain diseases.
1619
01:41:36.000 --> 01:41:38.239
It's not going to make you live to one fifty
1620
01:41:38.319 --> 01:41:42.279
or one thousand or a million years. So within the game,
1621
01:41:43.039 --> 01:41:47.640
I'm less focused on being minutely accurate. I'm more focused
1622
01:41:47.920 --> 01:41:50.479
on accuracy and relative.
1623
01:41:50.079 --> 01:41:52.560
Terms, like what is it that you would really need
1624
01:41:52.600 --> 01:41:52.880
to do?
1625
01:41:52.920 --> 01:41:57.520
What kinds of interventions to reach that
indefinite, open ended
1626
01:41:57.600 --> 01:42:02.319
lifespan immortality if you will. And that's why I not
1627
01:42:02.439 --> 01:42:05.720
only include the rejuvenation therapies. I include other causes of
1628
01:42:05.760 --> 01:42:09.920
death too, and the opportunity to fight those, which you
1629
01:42:10.000 --> 01:42:13.239
will have more time to do if you're ageless. So
1630
01:42:13.600 --> 01:42:17.760
think about all the risks facing humanity and the effect
1631
01:42:17.840 --> 01:42:19.680
size of each of them.
1632
01:42:20.479 --> 01:42:24.199
Okay, if there is one question, and also I want
1633
01:42:24.279 --> 01:42:27.960
death to ask a question. Death, come here, I want
1634
01:42:28.000 --> 01:42:30.960
you to ask a question to our panelies. So think
1635
01:42:30.960 --> 01:42:33.199
about that question. Well we have a quick one, right,
1636
01:42:33.319 --> 01:42:35.840
quick one, and then death think about it because it
1637
01:42:35.960 --> 01:42:38.359
is a matter of life or death.
1638
01:42:41.000 --> 01:42:43.560
He said, we don't want to boxing match with the religion,
1639
01:42:43.600 --> 01:42:45.760
but what if that religion wants to fight us, and
1640
01:42:45.840 --> 01:42:51.560
particularly they if they like they oppose cryonics for example.
1641
01:42:52.680 --> 01:42:58.159
Yes, what if those who are religious or of certain
1642
01:42:58.199 --> 01:42:59.840
religious persuasions want to fight us?
1643
01:43:00.039 --> 01:43:01.960
That's the question, Joe, go ahead, and I have some
1644
01:43:02.000 --> 01:43:02.560
thoughts to it.
1645
01:43:04.399 --> 01:43:07.119
Yeah, it's still it's still not a good strategy. Okay,
1646
01:43:07.319 --> 01:43:09.439
we you know, there's there's a lot of people who
1647
01:43:10.640 --> 01:43:12.199
it's just not the way we want to go. There's
1648
01:43:12.479 --> 01:43:14.159
there's a lot of people like in the middle ground
1649
01:43:14.239 --> 01:43:16.760
that we just want to bring around to our our
1650
01:43:18.279 --> 01:43:21.319
to understand what we're doing. And that's what we need
1651
01:43:21.359 --> 01:43:24.239
to keep going with. And yeah, yes, it's still the
1652
01:43:24.279 --> 01:43:26.960
best way to go. And my view is fight the dogmatism.
1653
01:43:27.159 --> 01:43:31.720
Don't fight the core of their faith or their religious tradition,
1654
01:43:32.239 --> 01:43:35.000
but fight against the fact that they want to impose
1655
01:43:35.079 --> 01:43:39.039
their views on others. And I have a rather strong
1656
01:43:39.399 --> 01:43:41.680
libertarian strict small L, not capital L.
1657
01:43:41.920 --> 01:43:44.119
But I believe in individual freedom.
1658
01:43:44.199 --> 01:43:46.479
I believe in your right to make the choices that
1659
01:43:46.560 --> 01:43:49.279
you want to make for your life and your well
1660
01:43:49.319 --> 01:43:53.680
being as a patient, as a health and wellness enthusiast,
1661
01:43:53.720 --> 01:43:57.720
as a cryonicist. So the argument from individual rights will
1662
01:43:57.760 --> 01:44:02.000
resonate with a lot of both secular and religious individuals.
1663
01:44:02.159 --> 01:44:05.479
And you can appeal to a lot of people who
1664
01:44:05.600 --> 01:44:08.640
might even be say, fundamentalists, but tell them, well, what
1665
01:44:08.720 --> 01:44:10.119
about the US Constitution?
1666
01:44:10.199 --> 01:44:11.279
What about the Bill of Rights?
1667
01:44:11.279 --> 01:44:14.600
What about what the founders wanted individuals.
1668
01:44:14.119 --> 01:44:15.640
To enjoy us their freedom?
1669
01:44:16.000 --> 01:44:20.640
Okay, now I want to say something to okay quickly. Also,
1670
01:44:20.840 --> 01:44:22.560
you got to look at the silver lining of people
1671
01:44:22.680 --> 01:44:27.199
fighting us, because that's actually progress because first things are ridiculed,
1672
01:44:27.439 --> 01:44:30.840
then they're violently opposed, and then is widely accepted as truth.
1673
01:44:31.239 --> 01:44:33.439
So we're making progress when they're fighting us.
1674
01:44:34.159 --> 01:44:36.960
Yeah, very good. Sir Arthur S.
1675
01:44:37.079 --> 01:44:41.399
Clark who said that anyway, death has the final question,
1676
01:44:42.000 --> 01:44:44.840
so it must be an immortal question.
1677
01:44:45.720 --> 01:44:48.399
I realize I strike a lot of your hearts with
1678
01:44:48.560 --> 01:44:53.439
anxiety and fear. How death do you want to ameliorate that.
1679
01:44:58.760 --> 01:44:59.640
I didn't understand it?
1680
01:45:00.000 --> 01:45:02.920
Well, I don't know if I want to alleviate the
1681
01:45:03.000 --> 01:45:06.479
fear of death as long as you exist, because fear
1682
01:45:06.880 --> 01:45:10.640
can be a powerful motivator. Now, I've been asked this
1683
01:45:10.760 --> 01:45:13.399
question a lot since I published Death Is Wrong.
1684
01:45:13.479 --> 01:45:16.760
Well, aren't you doing all this just because you're afraid
1685
01:45:17.119 --> 01:45:17.600
to die?
1686
01:45:18.239 --> 01:45:20.560
I don't deny that I'm afraid to die, but I
1687
01:45:20.680 --> 01:45:23.640
have to go deeper than that, and I have to ask, well,
1688
01:45:23.640 --> 01:45:27.039
if I'm afraid of something, why is it that I'm afraid?
1689
01:45:27.600 --> 01:45:31.600
What is it that I'm afraid to do or become?
1690
01:45:32.199 --> 01:45:35.600
I'm afraid to lose something good. I'm afraid to lose
1691
01:45:35.800 --> 01:45:39.199
life because life is good. Why am I afraid to
1692
01:45:39.199 --> 01:45:39.720
lose life?
1693
01:45:39.760 --> 01:45:40.800
Because I love life?
1694
01:45:40.880 --> 01:45:43.640
So I think fear of death isn't something to be
1695
01:45:43.960 --> 01:45:47.600
ashamed of. Fear of death stems from love of life,
1696
01:45:47.640 --> 01:45:50.039
and love of life is something that should be embraced.
1697
01:45:50.239 --> 01:45:50.680
Well.
1698
01:45:50.600 --> 01:45:57.920
As people, we need adapt to adapt to some kind
1699
01:45:57.960 --> 01:46:00.520
of catalyst in life, and we've really don't.
1700
01:46:00.600 --> 01:46:03.439
And so I would say, let's not make death the
1701
01:46:03.439 --> 01:46:06.800
catalyst of our movement. Uh, you know, I I think
1702
01:46:06.840 --> 01:46:09.479
that what Jim was talking about on the main stage.
1703
01:46:09.479 --> 01:46:12.079
I think it was Opening Night about about being.
1704
01:46:11.920 --> 01:46:17.039
Drawn to to because to consider ourselves pre human, about
1705
01:46:17.039 --> 01:46:20.600
being drawn to what will be our true human state,
1706
01:46:20.680 --> 01:46:24.479
which is which is what would be considered heaven on Earth.
1707
01:46:24.479 --> 01:46:26.760
But it's really it's really what Earth should be.
1708
01:46:27.199 --> 01:46:31.199
Ha ha yeah yeah, yeah yeah. Don't don't take it,
1709
01:46:31.319 --> 01:46:33.199
don't take it wrong. But uh.
1710
01:46:35.239 --> 01:46:37.800
I read the folks enjoy abundance.
1711
01:46:37.279 --> 01:46:40.720
And beautiful, beautiful Jim.
1712
01:46:40.800 --> 01:46:44.000
Actually, when people say that what gives meaning to life
1713
01:46:44.199 --> 01:46:47.600
is death, that is so stupid. It's like saying, what
1714
01:46:47.760 --> 01:46:52.800
gives meaning to marriage is divorce. No, what gives meaning
1715
01:46:52.880 --> 01:46:56.399
to marriage is marriage. What gives meaning to life is
1716
01:46:56.560 --> 01:47:01.039
life more life. So we are going, fine, we are
1717
01:47:01.079 --> 01:47:04.920
going to lunch. We are go and take some pictures
1718
01:47:05.359 --> 01:47:07.960
because this is for immortality and he's a very good
1719
01:47:07.960 --> 01:47:08.640
look in death.
1720
01:47:09.560 --> 01:47:11.159
So have some pictures with death.
1721
01:47:11.640 --> 01:50:20.479
Also, Happy lunch, Sa