And I'm obligated to point out that we were the first to invent a SARSCoV2 protease inhibitor with the essential elements later found in Paxlovid (we showed our drugs in 9/2020, Pfizer announced Paxlovid in 4/2021)
It's commonly misreported that Pfizer was able to make Paxlovid quickly because they had SARSCoV1 protease inhibitors from 2005. That is absolutely false. Paxlovid did not derive from their prior work. It was derived from our or other labs' work in 2020.
Pfizer's earlier SARSCoV2 protease inhibitor, PF-00835231, indeed came from their earlier SARSCoV1 work. But this is an IV-only drug and testing was stopped after Pfizer saw our work (or others') that the HCV protease inhibitor boceprevir can be modified into a SARSCoV2 inhibitor
That's why Pfizer's drug is chemically similar to our ML1000 announced in September 2020. Most of our drug, and theirs, derives from the off-patent boceprevir., which we and other academic labs found to have the right shape to bind the SARSCoV2 protease.
So I'm happy that Pfizer made Paxlovid, as it's a good drug. I'm also happy that academic labs such as ours provided information that pharma companies could use to accelerate the search for treatments. It's what academics do.
Thus it's important to recognize the role of academic research in Paxlovid's development. We've already acknowledged it for vaccine development, so really it should be no surprise it can also occur for therapeutics.
And many academics are doing COVID19 work on a volunteer basis. My lab has yet to receive any funding from NIH for our protease inhibitor research, for example. And we explore questions big pharma thinks aren't productive, and we make our findings public. That's an excellent ROI.
We received funding for SARSCoV2 work from Fast Grants from @patrickc, @Stanford_ChEMH, and the @Stanford Coulter program. It's been enough funding for 1 person essentially, vs 300 scientists Pfizer has put on it.
In short, where did Pfizer's ideas come from? See and decide for yourself.
History A: as told by Pfizer
History B: more parsimonious (typical academic understatement)
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Would you prefer (1) we get back to normal activities sometime, or (2) we make new vaccine-evading coronaviruses continuously, suffer widespread breakthrough waves, and wear masks forever?
If you chose #1, then know this: Merck's molnupiravir should not be approved.
Molnupiravir is, to put it in clear terms, a potentially dangerous and virus-enhancing drug. It is not an effective antiviral medication outside of the confined conditions of cell culture and hamster cages. I'll explain below.
Well known independent voices have brought this up, such as @CT_Bergstrom (renowned skeptic of bad research) @WmHaseltine (HIV pioneer) and @JamesEKHildreth (FDA advisor). Others such as @chasewnelson have done more in-depth analysis. I'm here to try to explain the issue simply.
I've been meaning to reveal some exciting results from my lab's SARSCoV2 protease inhibitor research. With FDA approval of Pfizer's Paxlovid today, it's a good time to finally share our good news as well.
We've developed not 1 but 2 inhibitors with activity superior to Paxlovid.
This work began in March 2020 when we hypothesized the HCV protease inhibitor boceprevir could serve as a template for the creation of orally dosable SARSCoV2 protease inhibitors. We announced initial results from this work in September 2020.
Our initial drug, ML1000, described in 2020 September, preceded Pfizer's PF-07321332 (Paxlovid) announced in 2021 April and approved today. Other groups have also made drugs with boceprevir parts, but our drug is the closest in structure to PF-07321332
@b_chinnian5 Importantly, they said the vast majority of hospitalized cases were unvaccinated. But SA has a high rate of seroprevalance, >70% per some studies. So worst-case interpretation here is everyone hospitalized was either vaccinated or unvaccinated but previously infected.
Meta-thread (trying to keep tweets organized by topic)
2020.03: The #coronadeck, in which I explained that we knew a lot about SARSCoV2 because it's 80% identical to SARSCoV1. Discussed evidence for the usefulness of masks, previewed possible Rx, etc
2020.07: Proposing that preadolescent children should be considered separately from adolescents, and hypothesizing that they may have milder disease because of stronger innate immunity.
Study design is excellent. Relevant vaccine statuses were tested in parallel: {Moderna, Pfizer, J&J} x {distant vax, recent vax, infection+vax, boosted vax}. Assay was pseudovirus neutralization. Color-coded images explain everything.
Also there's a very informative diagram of what was actually done. A picture not just says 1000 words, but is so much easier to understand and prevents confusion about what reagents and procedures were used, so hoping this becomes more common in papers.
When we discovered boceprevir has activity against SARSCoV2, we contacted Merck and let them know, because it was their drug and we figured they could modify the compound for even better activity.
Well Merck didn't pursue a boceprevir derivative for COVID19, and chose instead to bet on a new drug that creates mutations in the virus as its only mechanism of action. This had never been tried before (there's a belief ribavirin does, but it has other inhibitory effects).