The @StanfordDaily reached out to Science and @Nature, where another of Tessier-Lavigne’s papers containing alleged data alteration was published, for comment. @ScienceMagazine's editor-in-chief @hholdenthorp wrote in an email that he would “check around.”
Marc Tessier-Lavigne’s papers with issues confirmed by the University have accrued tens of thousands of downloads and include some of his most cited work in neurobiology. None of the papers has been retracted or corrected @tab_delete@StanfordDaily#scipol
“I can tell you right now, I recognize the pattern because it happens all the time. They’re gonna have an internal, non-expert, conflicted, confidential investigation, and then guess what? They’re gonna [not impose any consequences]”-@DrNancyOlivieri#RRI
“There are potential problems with data in a few studies which may warrant investigation and correction, but these concerns do not appear to represent a systematic issue throughout Tessier-Lavigne’s extensive and influential body of work” @schrag_matthew stanforddaily.com/2022/11/30/sta…
The newly identified apparent manipulation in Cell is especially serious as it seems to alter the results and appears to be intentional, said @MicrobiomDigest. “I would testify in court that’s been digitally altered. This actually changes everything." statnews.com/2022/11/30/sta…
Concerns relating to images in at least four papers of Tessier-Lavigne’s — two of which listed him as senior author — date back to at least 2001 and have been publicly raised for years on @PubPeer, a website where people point out anomalies about research
@JeremyFarrar: (laughs) If I knew, I'd be a @NobelPrize candidate–or a multibillionaire...
It would be a once-in-a-lifetime vaccine like the one against measles,
it would cost a cent,
it would block transmission spiegel.de/international/…
Is it still possible to find a vaccine for this soup of different variants? @JeremyFarrar: We have to get ourselves out of that situation. And I think the only way we're going to get ourselves out of that is the generation of vaccines @bredow@VHackenbroch
How realistic is it that a perfect vaccine will materialize?
Farrar: Is it possible today? No, certainly not. Would it be possible this decade? Possibly not yet either.
If the political class moves on & pretend it's over, I fear, that investment won't come
We have tested the antibody in various doses on 856 patients on 3 continents. After only 6 months we observed positive results, and after 18 months 81% of the group receiving the highest dosage showed lower levels of amyloid beta than the level we measure in Alzheimer’s-Lannfelt
“The idea for the antibody originated back in the 1990s, when the team identified a change in the genetic material of a Swedish family that had been severely afflicted by Alzheimer's disease. The mutation indicated that the cause seemed to be protofibrils” medicalxpress.com/news/2018-10-a…
Overnight a Swedish professor made $350 million. The lucky man, Lars Lannfelt, was not particularly famous. He had done pioneering work on Alzheimer’s, but it was in the 90s and belonged to a sub-field that, after a litany of failures had fallen from grace statnews.com/2022/10/11/for…
Right now, we're going after the pathology of the disease–plaques & tangles-but I think we need to start going after the biology and, as a result, the pharmacology that addresses the altered biology with aging that occurs in Alzheimer's-@a_hfillit@TheADDF biospace.com/article/ctad-2…
“The mixed data shows that while anti-amyloids are a promising starting point, we will need a combination of drugs aimed at different targets informed by the biology of aging to effectively treat this disease”
-@a_hfillit, M.D., co-founder and CSO @TheADDF fiercebiotech.com/biotech/roche-…
Today, almost half of the 4 million Americans living with type 1 diabetes use devices called continuous glucose monitors, or CGMs, to monitor their #glucose levels and regulate their insulin levels in real-time. @statnews' @KatieMPalmer reviews CGM's here: reports.statnews.com/products/conti…
@statnews unpacks the differences between the different ways the FDA approves drugs, like accelerated approvals, fast-track designations, and emergency use authorizations. It touches on how we got here, where the agency is headed next, and what's at stake reports.statnews.com/products/speed…
The potential of the psychedelics industry has never been bigger. Long-stigmatized drugs like esketemine, MDMA and psilocybin are advancing rapidly through clinical trials for treatments of a range of mental health conditions @OliviaGoldhill@statnews reports.statnews.com/products/the-s…
🧵Since the first β-lactam, aminoglycoside, macrolide, tetracycline, and fluoroquinolone classes of antibiotics were discovered and approved from 1940 to 1980, few #antibiotics with novel mechanisms of action have been developed @thomasmd@akesselheim#AMR science.org/doi/10.1126/sc…
Phase III clinical trials of a antibiotic in a single disease indication cost about US$70 million. Funding for biotech companies—venture capital or government grants—cannot cover this for a drug that will be sold mainly in short courses
Cooper M & Shlaes D nature.com/articles/47203…
@BradSpellberg, who studies infectious diseases, sums up the problem: We'll pay $50,000 for a course of cancer chemotherapy that prolongs life by 3 months, but we don't want to pay more than $100 for a course of antibiotics that cures the target infection nature.com/articles/509S4a
After 18 months, participants who received lecanemab scored, on average, 0.45 points better on the CDR-SB than those who got a placebo. Some researchers, however, have questioned whether this shift is big enough to make a noticeable difference in a person’s symptoms @meprillaman
It’s a modest benefit, says @BrentForester, director of the Geriatric Psychiatry Research Program @McLeanHospital who helped to run the clinical trial for lecanemab. His concerns lie with safety. About 20% of treated people had brain-scan anomalies #CTAD22
If a connection between lecanemab and the deaths is found, it could pose “a real conundrum” for the US Food and Drug Administration as it decides how to rule on lecanemab, says Caleb Alexander @JohnsHopkinsSPH and an advisory committee member for the FDA nature.com/articles/d4158…