Empowered Patient Podcast

Kelvin Cooper, CEO of Lakewood-Amedex Biotherapeutics, has developed a novel class of antimicrobials that operate by disrupting bacterial and fungal cell membranes, rapidly killing the microorganisms. Traditional antimicrobials work by inhibiting bacterial growth, but bacteria have evolved resistance mechanisms against all drug classes, with multidrug-resistant strains becoming increasingly common. The company is focused on treating infected diabetic foot ulcers with a topical gel formulation that locally delivers a high drug concentration while minimizing systemic side effects.

Kelvin explains, "You can go back all the way to the discovery of penicillin a century ago, and there was tremendous excitement around that. And then through the 40s, when they figured out how to deep tank ferment the antibacterials, the beta lactams, as it was then, again, there was no real indication that resistance was going to be that big of a problem."

"What we have done at Lakewood-Amedex Biotherapeutics is we've discovered a completely new class of antimicrobials, and it's probably good to give some context of how most antimicrobials work. Typically, what they do is they will stop the bacteria from dividing and growing, and that prevents the bacteria from causing an infection. Now the bacteria and fungi have figured out ways to mutate around that. So they have a different way of building cell walls, for example. And that has become the big problem. Our class of agents hits a completely different type of mechanism. We believe that what happens, and we have good scientific data to show this, is that this class of agents attacks the membrane of bacteria and fungi. It disrupts the membrane, which allows the contents of whatever microbe it is to spill out, and it immediately kills the bacteria extremely rapidly."

#LakewoodAmedex #AntimicrobialResistance #AMR #InfectiousDiseases #Antibiotics #Antimicrobials #DiabeticFoot #DiabeticFootUlcer #HealthcareInnovation #DiabeticCare #Biotech #PublicHealth #MedicalBreakthrough $LABT

lakewoodamedex.com

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Kelvin Cooper, CEO of Lakewood-Amedex Biotherapeutics, has developed a novel class of antimicrobials that operate by disrupting bacterial and fungal cell membranes, rapidly killing the microorganisms. Traditional antimicrobials work by inhibiting bacterial growth, but bacteria have evolved resistance mechanisms against all drug classes, with multidrug-resistant strains becoming increasingly common. The company is focused on treating infected diabetic foot ulcers with a topical gel formulation that locally delivers a high drug concentration while minimizing systemic side effects.

Kelvin explains, "You can go back all the way to the discovery of penicillin a century ago, and there was tremendous excitement around that. And then through the 40s, when they figured out how to deep tank ferment the antibacterials, the beta lactams, as it was then, again, there was no real indication that resistance was going to be that big of a problem."

"What we have done at Lakewood-Amedex Biotherapeutics is we've discovered a completely new class of antimicrobials, and it's probably good to give some context of how most antimicrobials work. Typically, what they do is they will stop the bacteria from dividing and growing, and that prevents the bacteria from causing an infection. Now the bacteria and fungi have figured out ways to mutate around that. So they have a different way of building cell walls, for example. And that has become the big problem. Our class of agents hits a completely different type of mechanism. We believe that what happens, and we have good scientific data to show this, is that this class of agents attacks the membrane of bacteria and fungi. It disrupts the membrane, which allows the contents of whatever microbe it is to spill out, and it immediately kills the bacteria extremely rapidly."

#LakewoodAmedex #AntimicrobialResistance #AMR #InfectiousDiseases #Antibiotics #Antimicrobials #DiabeticFoot #DiabeticFootUlcer #HealthcareInnovation #DiabeticCare #Biotech #PublicHealth #MedicalBreakthrough $LABT

lakewoodamedex.com

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Harith Rajagopalan, Co-Founder and CEO of Fractyl Health, is developing innovative therapies that target the root causes of obesity and metabolic diseases to achieve durable, long-lasting patient outcomes. Their drug is designed to address post-GLP-1 rebound weight gain by treating the underlying gut damage. Unlike GLP-1 medications that manage symptoms through appetite suppression, the aim is to modify the disease driving the obesity and change the paradigm from a symptomatic treatment to one of disease modification.

Harith explains, "Our focus at Fractyl is all about how to achieve durable results for patients, long-lasting benefits. And the way in which we try to do so is by targeting root causes of obesity and metabolic disease and developing innovative therapies, targeting those root causes that offer the potential for long-lasting benefit for patients."

"I think that GLP-1s have been transformative, as you say, but they have in many ways created an altogether new problem called post-GLP-1 rebound. What we are seeing in the United States right now is that there are a million people a month who are stopping a GLP-1. The more effective GLP-1 was for them in weight and metabolic control, the more rapidly they rebounded to whatever their weight and metabolic control were prior to treatment."

"Whereas what we are doing is with our lead asset, Revita, we are targeting a root cause of obesity in the gut, a region of the gut that becomes damaged by chronic lifetime exposure to high-fat, high-sugar diets that we think is actually driving the obesity in the first place. And so if you can fix the underlying obesity, then we think that you can prevent the rebound that inevitably occurs upon the discontinuation of the medicine."

#FractylHealth #Revita #Rejuva #PopulationHealth #ObesityMedicine #Endocrinology #MetabolicHealth #GLP1 #Gastroenterology #DiabetesCare #GeneTherapy

fractyl.com

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Harith Rajagopalan, Co-Founder and CEO of Fractyl Health, is developing innovative therapies that target the root causes of obesity and metabolic diseases to achieve durable, long-lasting patient outcomes. Their drug is designed to address post-GLP-1 rebound weight gain by treating the underlying gut damage. Unlike GLP-1 medications that manage symptoms through appetite suppression, the aim is to modify the disease driving the obesity and change the paradigm from a symptomatic treatment to one of disease modification.

Harith explains, "Our focus at Fractyl is all about how to achieve durable results for patients, long-lasting benefits. And the way in which we try to do so is by targeting root causes of obesity and metabolic disease and developing innovative therapies, targeting those root causes that offer the potential for long-lasting benefit for patients."

"I think that GLP-1s have been transformative, as you say, but they have in many ways created an altogether new problem called post-GLP-1 rebound. What we are seeing in the United States right now is that there are a million people a month who are stopping a GLP-1. The more effective GLP-1 was for them in weight and metabolic control, the more rapidly they rebounded to whatever their weight and metabolic control were prior to treatment."

"Whereas what we are doing is with our lead asset, Revita, we are targeting a root cause of obesity in the gut, a region of the gut that becomes damaged by chronic lifetime exposure to high-fat, high-sugar diets that we think is actually driving the obesity in the first place. And so if you can fix the underlying obesity, then we think that you can prevent the rebound that inevitably occurs upon the discontinuation of the medicine."

#FractylHealth #Revita #Rejuva #PopulationHealth #ObesityMedicine #Endocrinology #MetabolicHealth #GLP1 #Gastroenterology #DiabetesCare #GeneTherapy

fractyl.com

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Lior Shaltiel, CEO of NurExone, is addressing the unmet needs of those with spinal cord injuries, as current therapies only treat symptoms and do not regenerate damaged nerves from accidents or disease. The NurExone technology aims to stimulate nerve growth by targeting a protein that inhibits cell proliferation. Using exosomes, which are secreted by cells, to deliver the drug in a localized manner is possible because of the ability of the exosomes to home in on damaged tissues and cross the blood-brain barrier.

Lior explains, "At the moment, the medicine can only treat it by treating the symptoms. There are a few attempts to try to regenerate the nerves that are broken and to have the reconnection of the spinal cord injury or any damage in the central nervous system. And this is a huge challenge for medicine, so far not solved. And when we solve it, we prepare to answer and give hope to so many patients, not only in spinal cord injury, but also in other injuries, such as traumatic brain injury, optic nerve, and ophthalmology. So many nerves that we have so far not been able to restore the function after the damage."

"So traumatic, meaning we are talking about injury, the acute phase of a disease or illness. In most cases, let's say, spinal cord injury is due to injury, car accidents, or sports accidents. But, for example, ophthalmology, glaucoma, which is a chronic disease, can also cause damage to the optic nerve that cannot be restored. So it can be due to another illness, as a side effect of the illness, or due to injury."

"So we discussed the RNA. This is one part of the technology here. Second, the technology of using our natural transmitter in our body, which is how cells communicate with each other, is called exosomes. Exosomes are tiny vesicles secreted from cells with tiny envelopes that a healthy tissue sends to a damaged tissue, a cell that is affected, or a cell that doesn't feel good. And when we understand this mechanism, we can use those exosomes as a drug delivery system."

#NurExone #Exosomes #SpinalCordInjury #NeuroRegeneration #PTEN #siRNA #DrugDelivery #Neurology #RegenerativeMedicine #Nanomedicine

nurexone.com

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Lior Shaltiel, CEO of NurExone, is addressing the unmet needs of those with spinal cord injuries, as current therapies only treat symptoms and do not regenerate damaged nerves from accidents or disease. The NurExone technology aims to stimulate nerve growth by targeting a protein that inhibits cell proliferation. Using exosomes, which are secreted by cells, to deliver the drug in a localized manner is possible because of the ability of the exosomes to home in on damaged tissues and cross the blood-brain barrier.

Lior explains, "At the moment, the medicine can only treat it by treating the symptoms. There are a few attempts to try to regenerate the nerves that are broken and to have the reconnection of the spinal cord injury or any damage in the central nervous system. And this is a huge challenge for medicine, so far not solved. And when we solve it, we prepare to answer and give hope to so many patients, not only in spinal cord injury, but also in other injuries, such as traumatic brain injury, optic nerve, and ophthalmology. So many nerves that we have so far not been able to restore the function after the damage."

"So traumatic, meaning we are talking about injury, the acute phase of a disease or illness. In most cases, let's say, spinal cord injury is due to injury, car accidents, or sports accidents. But, for example, ophthalmology, glaucoma, which is a chronic disease, can also cause damage to the optic nerve that cannot be restored. So it can be due to another illness, as a side effect of the illness, or due to injury."

"So we discussed the RNA. This is one part of the technology here. Second, the technology of using our natural transmitter in our body, which is how cells communicate with each other, is called exosomes. Exosomes are tiny vesicles secreted from cells with tiny envelopes that a healthy tissue sends to a damaged tissue, a cell that is affected, or a cell that doesn't feel good. And when we understand this mechanism, we can use those exosomes as a drug delivery system."

#NurExone #Exosomes #SpinalCordInjury #NeuroRegeneration #PTEN #siRNA #DrugDelivery #Neurology #RegenerativeMedicine #Nanomedicine

nurexone.com

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Peter Swimm, Founder of Toilville, is a conversational AI pioneer, and he describes the transformation in healthcare resulting from the use of AI and large language models to address clinician burnout and improve patient outcomes. He emphasizes that technology should adapt to practitioners' workflows rather than forcing practitioners to change their behavior. Human oversight is essential to ensure accuracy and transparency, and Peter advocates for a culture shift where time saved through the use of AI is reinvested in higher-quality patient care and clinician satisfaction.

Peter explains, "I think a lot of people think of their problems as a unique snowflake in the world. I think if we boil the ocean down to its elements, it is an understanding of the system of its inhabitants. And so we do a lot of work with small businesses and clients who typically have worked for big companies, and they've chafed at all the rules and the boundaries and the problems. They leave the big company and want to run their own show, but they lose that infrastructure."

"A lot of times, they turn to tools like AI and automation, or they buy software products that don't entirely fit their thinking. And so we help them negotiate that pattern where the technology molds to what the presentation layer is and how you want to treat things and handle your data. And you don't change away from what your competitive advantage is, which is being a unique and talented person who runs the show the way they see best."

"So I think the challenge is, don't let your FOMO be FAFO. Just because everyone's telling you to do AI and you don't really understand it and you don't see the positive outcomes, don't assume it's like a lack of training on your part."

#SPELWork #Toilville #OptInPodcast #ResonantDiversification #AIGovernance #ResponsibleAI #ConsentFirst #DigitalHealth #HealthTech #HealthIT #ClinicalAI #HealthcareAI #PatientAdvocacy #ClinicianBurnout #HealthEquity #SDOH #AIAccountability #AIEthics #AISafety #ConsentFirst #DataSovereignty #HumanInTheLoop #HealthcareInnovation#DigitalHealth #PhysicianBurnout #HealthIT #ConversationalAI #PatientCare

toilville.com

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Peter Swimm, Founder of Toilville, is a conversational AI pioneer, and he describes the transformation in healthcare resulting from the use of AI and large language models to address clinician burnout and improve patient outcomes. He emphasizes that technology should adapt to practitioners' workflows rather than forcing practitioners to change their behavior. Human oversight is essential to ensure accuracy and transparency, and Peter advocates for a culture shift where time saved through the use of AI is reinvested in higher-quality patient care and clinician satisfaction.

Peter explains, "I think a lot of people think of their problems as a unique snowflake in the world. I think if we boil the ocean down to its elements, it is an understanding of the system of its inhabitants. And so we do a lot of work with small businesses and clients who typically have worked for big companies, and they've chafed at all the rules and the boundaries and the problems. They leave the big company and want to run their own show, but they lose that infrastructure."

"A lot of times, they turn to tools like AI and automation, or they buy software products that don't entirely fit their thinking. And so we help them negotiate that pattern where the technology molds to what the presentation layer is and how you want to treat things and handle your data. And you don't change away from what your competitive advantage is, which is being a unique and talented person who runs the show the way they see best."

"So I think the challenge is, don't let your FOMO be FAFO. Just because everyone's telling you to do AI and you don't really understand it and you don't see the positive outcomes, don't assume it's like a lack of training on your part."

#SPELWork #Toilville #OptInPodcast #ResonantDiversification #AIGovernance #ResponsibleAI #ConsentFirst #DigitalHealth #HealthTech #HealthIT #ClinicalAI #HealthcareAI #PatientAdvocacy #ClinicianBurnout #HealthEquity #SDOH #AIAccountability #AIEthics #AISafety #ConsentFirst #DataSovereignty #HumanInTheLoop #HealthcareInnovation#DigitalHealth #PhysicianBurnout #HealthIT #ConversationalAI #PatientCare

toilville.com

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Richard Garr, CEO and General Counsel of Curative Biotechnology, discusses the company's work in repurposing the diabetes drug metformin into an eye drop for degenerative eye diseases. The goal of the therapy is retinal preservation, aiming to slow or stop disease progression by acting at the cellular level in the back of the eye to protect it from damage, offering a non-invasive alternative to current treatments. Using a repurposed drug allows the company to build on well-documented safety data and reduces the size, cost and duration of clinical trials.

Richard explains, "We are currently focused on repurposing the drug metformin, which is an FDA-approved drug that diabetics take. And as it turns out, we have reformulated it into an eye drop. This is licensed from the National Eye Institute. We have worldwide exclusive rights. The first patent in that estate was allowed about two months ago in Canada. We would expect it to be issued this summer. It's being prosecuted around the world."

"We believe that it is a platform drug and that we'll be able to treat a wide range of degenerative eye diseases. It's repurposed because it is an approved FDA drug. It's been taken for decades orally by literally tens of millions of patients, mostly with type two diabetes. And really, the importance of that is that we know it's a safe systemically. So, everything you could want to know about the metformin systemically is known. What we have to show in our clinical trials is that it's safe in the eye and that it does, in fact, do what we suspect it does to treat degenerative eye disease."

#CurativeBiotech #Ophthalmology #Retina #Neuroprotection #DryAMD #EyeCare #DrugRepurposing #Metformin #HealthcareInnovation #ClinicalResearch #CurativeBiotech

CurativeBiotech.com

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Richard Garr, CEO and General Counsel of Curative Biotechnology, discusses the company's work in repurposing the diabetes drug metformin into an eye drop for degenerative eye diseases. The goal of the therapy is retinal preservation, aiming to slow or stop disease progression by acting at the cellular level in the back of the eye to protect it from damage, offering a non-invasive alternative to current treatments. Using a repurposed drug allows the company to build on well-documented safety data and reduces the size, cost and duration of clinical trials.

Richard explains, "We are currently focused on repurposing the drug metformin, which is an FDA-approved drug that diabetics take. And as it turns out, we have reformulated it into an eye drop. This is licensed from the National Eye Institute. We have worldwide exclusive rights. The first patent in that estate was allowed about two months ago in Canada. We would expect it to be issued this summer. It's being prosecuted around the world."

"We believe that it is a platform drug and that we'll be able to treat a wide range of degenerative eye diseases. It's repurposed because it is an approved FDA drug. It's been taken for decades orally by literally tens of millions of patients, mostly with type two diabetes. And really, the importance of that is that we know it's a safe systemically. So, everything you could want to know about the metformin systemically is known. What we have to show in our clinical trials is that it's safe in the eye and that it does, in fact, do what we suspect it does to treat degenerative eye disease."

#CurativeBiotech #Ophthalmology #Retina #Neuroprotection #DryAMD #EyeCare #DrugRepurposing #Metformin #HealthcareInnovation #ClinicalResearch #CurativeBiotech

CurativeBiotech.com

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