
Coiled Therapeutics' Dr Sotirios Stergiopoulos on Roquefort RTO, AO-252 Cancer Trial Update
Coiled Therapeutics announced a reverse takeover of Roquefort Therapeutics, effectively relisting the clinical‑stage oncology company on the London market under the Coiled name. The transaction involves licensing the proprietary acid‑based drug AO‑252 from A2A Pharmaceuticals and raising £8.5 million to finance its next development phase. The newly raised capital will be directed almost entirely toward expanding the ongoing Phase I trial, targeting enrollment of 30‑50 patients by mid‑Q3 2026. Early data have shown tumor reductions with an exceptionally clean safety profile—no bone‑marrow suppression or liver toxicity—addressing a key limitation of existing chemotherapies for prostate and ovarian cancers. Dr. Sotirios Stergiopoulos highlighted that AO‑252’s safety enables longer continuous dosing and opens combination‑therapy opportunities, positioning the molecule as a potential monotherapy alternative to traditional chemotherapy. He also noted that successful trial read‑outs could trigger discussions with large pharmaceutical partners and broaden the drug’s indication landscape. If the trial confirms efficacy, AO‑252 could reshape solid‑tumor treatment by offering a less toxic option, attracting strategic alliances, and delivering value to shareholders through a differentiated oncology pipeline.

Avoiding, Treating & Curing Cancer With the Immune System | Dr. Alex Marson
In this Huberman Lab episode, Dr. Alex Marson explains how cutting‑edge biology is turning the immune system into a programmable weapon against cancer. He walks listeners through the fundamentals of innate and adaptive immunity, the random generation of T‑cell receptors,...

NEJM This Week — March 5, 2026
NEJM This Week highlighted several pivotal developments. A phase‑3 trial showed finerenone slows kidney disease in type‑1 diabetes patients, while new guidelines recommend early PCI of non‑culprit lesions after STEMI. The episode also introduced an investigational gene‑therapy for Dravet syndrome...

ARPA-H Funding, Brain Wearables, & Nanotech Biosensing | Longevity News Roundup — Week 10, 2026
The U.S. ARPA‑H agency announced a $144 million PROSPR program to accelerate human health‑span trials, awarding $30.8 million to Cambrian BioPharma for a next‑generation rapamycin analog and $22 million to Linnaeus Therapeutics for repurposed oncology drugs. Meanwhile, startups are pushing wearable and digital...

Life Sciences Consulting Explained | Careers, AI, and Industry Trends (2026)
A recent Management Consulted panel brought together leaders from Guidehouse, Clarkston Consulting, ClearView Healthcare Partners, and Roland Berger to dissect the current state of life‑sciences consulting. The discussion highlighted how artificial intelligence is delivering tangible value in drug development, how precision...

Meet Hepatologist Michael Schilsky, MD
The video features hepatologist Michael Schilsky, MD, outlining how liver transplantation has progressed from a pioneering procedure in the 1970s to a routine component of modern hepatology. He explains that transplants now address both severe acute liver failure and, more...

Adeno-Associated Virus-Mediated Gene Therapy - Advances, Immune Challenges, and Research Innovations
At FDA Grand Rounds, Dr. Ronit Mazur of CBER reviewed advances and persistent immunological challenges in adeno-associated virus (AAV)–mediated gene therapy, outlining how AAV’s favorable safety and durability have driven a surge in FDA approvals since 2017. She summarized AAV...

Healey Community Q&A Webinar: February 12, 2026 | Expanded Access
The Healey Community Q&A Webinar on February 12, 2026 featured Dr. James Berry of Massachusetts General Hospital alongside Rapa Therapeutics representatives. They reported that the RAPA-501 Expanded Access Protocol has successfully reached its enrollment goals, providing broader treatment options for...

Blum Center Program: Understanding Osteoarthritis - Keeping Your Joints Moving
In a February 23 2026 presentation, Dr. Avira Som of Massachusetts General Hospital explained osteoarthritis fundamentals, highlighted common symptoms, and reviewed current treatment options ranging from NSAIDs to intra‑articular injections. She also introduced emerging research on glucagon‑like peptide-1 (GLP‑1) receptor agonists and...

Making Biologics Orally Available With Vivtex's Thomas Von Erlach, Ph.D.
The interview with Thomas von Erlach, Ph.D., co‑founder and CEO of Vivex, focuses on the company’s breakthrough gastrointestinal‑on‑a‑chip platform that makes biologic drugs orally bioavailable, a stark contrast to traditional injections or IVs. Von Erlach outlines how the technology, conceived...

HIMS Core Business Faces Challenges in Guidance, GLP-1 Prices & NVO
Hims & Hers reported Q4 results after the bell, with mixed performance, drawing investor focus on its GLP‑1 program and forward guidance. The company posted EPS of $0.08, double expectations, but revenue of $617 million fell short of the $619 million forecast. For...

AI Insights in Pharma with Protai - Life Sciences Today Podcast Episode 50
In episode 50 of the Life Sciences Today podcast, host Danny Lieberman sits down with Carol Pesner, CTO and co‑founder of ProtAI, to discuss the company’s AI‑driven approach to drug discovery. ProtAI fuses structural proteomics with advanced artificial intelligence to...

🎙️ Targeting Inflammaging with AI
Scienta introduced EVA, an AI model designed to combat inflammaging. EVA integrates multi‑omic preclinical and clinical data to map inflammatory pathways linked to age‑related diseases. The platform proposes novel therapeutic targets and compounds aimed at restoring youthful immune signaling. The...

Don't Do THIS on a GLP-1? | What the Fitness | Biolayne
The video challenges a claim that artificial sweeteners trigger insulin spikes and hypoglycemia in people taking GLP‑1 medications. The host, a plastic surgeon presenting himself as a GLP‑1 expert, argues that the brain misinterprets sweeteners as sugar, prompting an insulin...

Nanoplastics, mRNA Therapy, & Drug Approvals | Longevity News Roundup — Week 9, 2026
Recent longevity news highlights nanoplastics in brains, a pioneering mRNA therapy, and regulatory shifts accelerating anti‑aging drug development. Researchers found ultra‑small plastic particles accumulating in Alzheimer‑affected brain tissue, independent of age. Klothea launched a phase 1b trial of AKL003 mRNA to...

LIVE: WHO Meeting on 2026-27 Northern Hemisphere Influenza Vaccine Composition
The World Health Organization convened an information meeting to finalize the composition of the 2026‑27 Northern Hemisphere influenza vaccine. Senior officials, including Dr. Chikui Hikawazu and Dr. Maria Van Kokov, highlighted the critical role of the Global Influenza Surveillance and...

3 Things to Know About Moderna’s mRNA Flu Vaccine and Its FDA Application
The video examines the FDA’s sudden reversal on Moderna’s mRNA influenza vaccine, shifting from an initial refusal to a green light for a fast‑track review aimed at adults aged 65 and older. The agency had already examined the application, but...

Walk With Me: Joseph Wu, Cardiologist Studying Stem Cells and Heart Disease
Joseph Wu, a Stanford professor of medicine and radiology, leads the Stanford Cardiovascular Institute in developing patient‑specific cardiac cells derived from a person’s own blood. By reprogramming blood cells into pluripotent stem cells and then coaxing them to become beating...

Health Compass | Season 3
Season 3 of Stanford Medicine’s Health Compass podcast, hosted by Dr. Maya Adam, examines how scientific discoveries move from the lab to patient care. Episodes pair engineers, data scientists, and clinicians to unpack translational hurdles in rare genetic diseases, stroke,...

Butterfly Skin: Caring for Patients with Epidermolysis Bullosa | Ep.1: Health Compass Podcast
The Health Compass podcast’s first episode spotlights epidermolysis bullosa, a rare genetic skin disorder often called “butterfly skin,” that makes even light touch painful. Stanford clinicians Jean Tang, MD, PhD, and Peter Marinkovich, MD, discuss how decades of research are...

A New Spin on Stroke Treatment | Ep.3: Health Compass Podcast
A stroke caused by a blocked artery demands immediate, precise intervention, as minutes dictate outcomes. At Stanford, radiologist Jeremy Heit and mechanical engineer Renee Zhao have joined forces to redesign clot removal using image‑guided, minimally invasive technologies. Their work leverages...

How a Winding Path Led to a Life-Saving Test | Ep.2: Health Compass Podcast
Purvesh Khatri, a Stanford professor with a background in electronics, software, and computational immunology, unveiled a rapid blood test that detects sepsis within minutes. The assay shortens diagnosis time dramatically, enabling clinicians to start targeted therapy far earlier than traditional...

Malta as a Living Lab for Precision Oncology | MedTech World Middle East 2026
At MedTech World Middle East 2026, Prof. Christian Scerri unveiled a plan to turn Malta into a living lab for precision oncology, leveraging its single national health system, compact ecosystem, and EU‑aligned regulatory framework. He outlined a roadmap that includes...

GCC MedTech Boom: Market, Funding & Scaling | MedTech World Middle East 2026
At MedTech World Middle East 2026, a panel of GCC health leaders highlighted the region’s rapid shift from a pure healthcare consumer to a burgeoning hub for MedTech, biotech, and digital health innovation. National visions and transformation strategies are driving...

Citi Bearish On Dr Reddy's; CLSA Positive On HAL, Says Company Has Strongest Pipeline Of Orders
Citi’s research team issued a bearish stance on Dr Reddy’s Laboratories, citing concerns that the company’s generic version of semaglutide may not capture significant market share. In contrast, CLSA upgraded Hindustan Aeronautics Limited (HAL) to a preferred pick, highlighting its strongest...

The Surprising Impact of Drug Price Negotiation on Clinical Trials
The podcast examines a new Health Affairs paper that tracks how the Inflation Reduction Act’s Medicare drug‑price negotiation provision has affected biopharmaceutical clinical‑trial activity. Dr. So Young Kang and co‑authors compare industry‑sponsored trial initiations from 2015‑2024, focusing on firms directly hit...

The Conjugation Conundrum: The Realities of Conjugated LNP Manufacturing
The discussion centers on the emerging complexities of conjugated lipid nanoparticle (LNP) manufacturing, a shift from standard platform processes toward targeted RNA delivery. Sujit explains that adding a biologic ligand to LNPs forces manufacturers to revisit every process parameter—viscosity, shear...

The “Art” Of the Linker: Complexity, Biodegradability, and Scale in Active LNP R&D
The panel examined the emerging “active” delivery paradigm for lipid nanoparticle (LNP) therapeutics, focusing on the added layers of complexity introduced by ligand‑modified formulations and the need for robust R&D pipelines. Participants contrasted passive LNPs with active, ligand‑decorated versions, highlighting...

The Challenges Novel Lipids Pose For mRNA-LNP Manufacturing
Novel lipid chemistries are accelerating mRNA‑LNP innovation, but they also upend established manufacturing platforms. According to CMC consultant Sujit Jain, each new lipid class forces a fresh round of process development, demanding new impurity profiling strategies and vendor qualification. The...

Novel Lipid Chemistries & Their Impact on Passive LNP Delivery
In a recent Advancing RNA Live session, Dominik Witzigmann of NanoVation and John Zuris of Stealth Co dissected emerging lipid chemistries that enhance passive lipid nanoparticle (LNP) delivery. They highlighted breakthroughs in ionizable lipids, helper lipids, and PEG‑lipids that improve...

How Microfluidics & QbD Are Maturing LNP Manufacturing
In a recent discussion, CMC consultant Sujit Jain and NanoVation CEO Dominik Witzigmann highlighted how microfluidic platforms combined with Quality‑by‑Design (QbD) principles are transforming lipid nanoparticle (LNP) production for mRNA therapeutics. They noted that continuous‑flow microfluidics now enable precise control...

Primates, Patents, & Progress: Advancements In Rational LNP Design
In a recent Advancing RNA Live segment, Dominik Witzigmann of NanoVation Therapeutics and John Zuris of Stealth Co discussed the latest scientific breakthroughs shaping lipid nanoparticle (LNP) design. They highlighted rational, data‑driven approaches that improve particle stability, targeting precision, and...

The Evolving CMC Landscape for mRNA-LNPs
In a recent Advancing RNA Live segment, CMC consultant Sujit Jain outlined the current maturity levels across process development, analytical methods, and supply‑chain logistics for mRNA‑LNP products. He highlighted that COVID‑19 vaccines and liver‑targeted therapeutics now operate on a reproducible,...

How the Health Technology Access Programme (HTAP) Operates?
The World Health Organization’s Health Technology Access Programme (HTAP) is designed to close the gap between high‑income manufacturers and low‑ and middle‑income countries that struggle with limited production capacity, skilled workforces, and costly health products. By convening technology owners, local...

FDA Direct: Combating Rare Diseases at the FDA
The FDA Direct town hall marked Rare Disease Day with a candid conversation between FDA leaders Jim and Elizabeth, who both have personal ties to rare‑disease advocacy. Their discussion highlighted the agency’s growing focus on rare‑disease patients, the establishment...

The Hidden Link Between Inflammation and Cholesterol | Behind the Breakthrough
The video explains that atherosclerotic plaque is primarily driven by chronic inflammation rather than merely cholesterol accumulation, highlighting a paradigm shift in heart‑disease research. Researchers at NYU Langone discovered that macrophages ingest cholesterol using receptors meant for bacteria, which stalls the...

NIH SciBites: Pursuing Lab-Grown Organs Through Stem Cell Studies
The video spotlights NIH post‑baccalaureate fellow Jack’s work on engineering lab‑grown organs, focusing on how stem cells must be coaxed through differentiation to become functional heart, lung or other tissues. Jack explains that differentiation hinges on the three‑dimensional arrangement of DNA....

HIMS Headwinds Ahead of Earnings
Hims & Hers (HIMS) heads into earnings amid legal and product challenges. The company faces a lawsuit from Novo Nordisk over its semaglutide weight‑loss offering and heightened regulatory scrutiny. Analysts say the upcoming call will be critical for investors seeking...

Regulatory Evolution to Expedite Drug Development in Japan: A PMDA Initiatives
The video outlines PMDA’s latest regulatory reforms aimed at accelerating drug development in Japan. Since its 2004 inception, the agency has cut review cycles dramatically, yet a growing “drug loss” problem persists as 35% of drugs approved in the United...

Knowing How Injection Volumes Impact Delivery Options
The panel discussed how the volume that can be self‑administered determines whether a therapy is delivered via a pre‑filled syringe (PFS), an autoinjector, or an infusion system. Speakers emphasized that the deciding factor is the drug’s pharmacokinetic profile. Antibodies that merely...

Relying On Human Factors Clinical Data For Regulatory Approvals
The discussion centered on the growing regulatory focus on human‑factors engineering in medical‑device submissions, especially within the FDA’s Center for Devices and Radiological Health. Participants noted that the agency’s human‑factors experts have become more visible over the past decade, and...

Preparing Early For Regulatory Marketing Submissions
The video addresses how companies should begin planning regulatory marketing submissions well before a product reaches the market, emphasizing patient‑centricity and the imperative of rapid access to therapies. It argues that early alignment of clinical trial design with the data...

Monitoring Patient Preferences And Post-Market Safety
The Drug Delivery Leader Live panel highlighted the growing emphasis on patient‑centric post‑market surveillance for injectable, infused, and implanted therapies. Shannon Hoste explained how manufacturers now track patient preferences and safety outcomes after product launch. Real‑world data and digital tools...

Selecting Injection Devices And Platforms
During the Drug Delivery Leader Live webcast, chief editor Tom von Gunden asked panelist Fran DeGrazio how dosing considerations drive the choice of injection devices and platforms. DeGrazio explained that dose volume, drug viscosity, and administration frequency are the primary...

Confirming Study Approaches For Clinical Bridging
During the Drug Delivery Leader Live event, Chief Editor Tom von Gunden prompted panelist Beate Bittner to discuss patient‑centric considerations as drug and delivery products transition to clinical trials. Bittner emphasized that leveraging established platforms and data from previous studies...

Determining Dosing For IV Or Subcutaneous Delivery
In a Drug Delivery Leader Live session, panelist Beate Bittner discussed early‑stage formulation decisions from a patient dosing perspective, comparing intravenous (IV) and subcutaneous (SC) routes. She highlighted how drug stability, bioavailability, administration frequency, and patient convenience shape the choice...

Company Turnarounds And AI For Infectious Diseases With Seek Labs' Jared Bauer
Jared Bauer, co‑founder and CEO of Seek Labs, detailed his experience turning around biotech firms and launching an integrated AI‑diagnostic and CRISPR‑therapeutics platform for infectious diseases. He highlighted a proof‑of‑concept study against African Swine Fever that markedly reduced viremia in...

NEJM This Week — February 12, 2026
NEJM This Week (Feb 12 2026) highlights several pivotal studies, including promising phase‑III results for novel IgA nephropathy therapies and updated antithrombotic regimens after coronary stenting. Researchers identified the specific antigen driving rare vaccine‑associated clotting syndromes, while a case report underscored the...

Roundtable on PMTA Submissions for ENDS Products
The FDA’s Center for Tobacco Products convened a roundtable to walk participants through the pre‑market tobacco product application (PMTA) process for electronic nicotine delivery systems (ENDS). Director Matthew Farley opened the session, emphasizing two goals: to clarify the scientific data...