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.Jay Bhattacharya, MD, PhD on false JAMA study claiming 383 clinical trials were terminated by NIH: “The reality is — at most — something like a dozen clinical trials actually were terminated…[the JAMA study] is based on an inaccurate list that didn’t take into account the fact that we...

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Dr. Ruxandra Teslo argues America's biotech problem isn't the science, it's how slowly we learn from humans: "This is going to be more and more of a bottleneck as science advances especially in oncology. It's not just that we don't have enough clinical trials and they are expensive. This has become worse and worse throughout the years." "The article is particularly focused on these phase one clinical trials. These are the trials where you first take a new drug into humans for the first time. The reason we're focusing on those, they are some of the most important trials because that's where you can actually start to learn and do iterative loops of learning in humans." "What you learn from that goes back into the science and you can engineer something better. We can see from China, they're very very good doing their phase one trials fast, that is very much responsible for propelling them ahead, almost ahead of the US in just a decade, despite the fact that their science is not as good." "We have a very good model for how to do them faster and better, which is Australia." Ruxandra Teslo 🧬 Adam Kroetsch IFP

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“I’m optimistic that HIV clinical trials will have a lot more diversity both in front of the lab coat and behind the lab coat.” – Tori Cooper We’re committed to ensuring the communities most impacted by #HIV are included in clinical trials.
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“I’m optimistic that HIV clinical trials will have a lot more diversity both in front of the lab coat and behind the lab coat.” – Tori Cooper We’re committed to ensuring the communities most impacted by #HIV are included in clinical trials.

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Dr. Jessica Rose explains how the mRNA used in clinical trials was made one way, but the commercial versions were switched to a cheaper, faster E. coli plasmid system. ”The products that people got as part of commercial products, that's like the billions of doses that went into most people are different from the ones that were trialed.” That means possible contaminants like toxic lipopolysaccharides and DNA were injected into everyone who got the shot. New product. No new trials. 📍The CHD 2025 Moment of Truth Conference in Austin, Texas. Jessica Rose 🤙

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Sen. Murray: You terminated a 23 year research effort to develop an HIV vaccine, just as scientists are on the cusp of a functional cure for HIV. You canceled a clinical trial evaluating new evidence-based interventions for Type 2 diabetes in Appalachia. You terminated a clinical trial to treat women with recurrent ovarian cancer. You're coming to us proposing to cut NIH funding by 40% next year. How many fewer clinical trials would you fund with a budget cut of $18 billion?
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🚨 Dr. Brian Hooker sounded the alarm on this 6-in-1 vaccine given to kids as young as two months: “Six infants died during the clinical trials.” “This doubled the chances of mortality if it was given at two months of life.” “It has no business being on the market.” “VAXELIS is a vaccine that is given starting at two months of age, and it has multiple antigens in it for diphtheria, tetanus, pertussis, polio, Hib, and Hepatitis B.” “It’s no surprise that six infants died during the clinical trials, and that this is buried.” “This type of information is buried.” “It is so unlike the way nature works.” “It’s so unlike the way the immune system was designed to work.” “We don’t queue up six different diseases and expose a child to all six of those diseases at the same time.” “But the public health authorities and the vaccine designers say, ‘It’s so convenient, it’s only one needle stick.’” “The concoction that they’ve put into this particular syringe is causing death.” Brian Hooker, PhD

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🚨🇺🇸DR PETER McCULLOUGH CALLS FOR MAJOR RANDOMISED TRIALS OF GENERIC DRUGS AGAINST CANCER This deserves serious scientific attention. Dr Peter McCullough is calling on the US National Cancer Institute and Britain's Medical Research Council to conduct large-scale clinical trials investigating a combination of generic medicines for solid-organ cancers. And he's not asking for a small observational study. He wants: Prospective. Double-blind. Randomised. Placebo-controlled trials. McCullough believes the existing evidence is sufficiently promising to justify putting the hypothesis through the highest level of clinical testing. That is precisely what should happen. If inexpensive, already-available medicines genuinely have significant anti-cancer effects, properly designed trials should be capable of demonstrating it. And if they don't, rigorous trials should establish that too. But McCullough raises another uncomfortable issue: Why isn't this receiving considerably more attention? He argues that pharmaceutical advertising exerts enormous influence over mainstream medical reporting — and questions whether that affects which potential treatments receive attention. Cancer affects millions of families around the world. If there is even a credible possibility that existing generic medicines could provide additional benefit, surely the answer isn't censorship or dismissal. RUN THE TRIALS. PUBLISH THE RESULTS. LET THE EVIDENCE DECIDE. McCullough Foundation Peter A. McCullough, MD, MPH® The Wellness Company

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