4 ms·
You are citing phase I data to support an implication that "clearly" phase 3 data was going to be positive. That is not how it works in real life. Many many
by hcknwscommenter 6y ago
You are citing phase I data to support an implication that "clearly" phase 3 data was going to be positive. That is not how it works in real life. Many many many drug candidates look great after phase 1 and fail to become approved drugs.
Also, we did double our microfluidic device capacity. We more than doubled it. We increased our capacity by something like a million fold. Before these vaccines (first of their kind), there was no commercial scale capacity. This has all been invented in the last year. There was even a chance that achieving such capacity would not be possible. It is fairly common that drug candidates that look promising in phase 1 or 2 simply cannot be manufactured at scale with the quality required to ensure consistent safety and efficacy.
- JamesBarney 6y agoModerna and Pfizer have been in the top 10 for a while, you could easily spend an extra billion on all of them and if half don't work out that's fine.
- Robotbeat 6y agoThat’s true about many drug candidates but not these. Moderna (and Pfizer) had EXTREMELY promising results from in vitro, primate, Phase I, and Phase II results. Success by Phase III was very, very likely.
- guyomes 6y agoI agree that the new drug candidates had promising results. Yet as a new technology, there was still a risk. For example, the first Pfizer drug candidate BNT162b1 gave fever to 75% of the participants in some cases [0]. Some countries decided not to buy from them at first for that reason. [0] https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7583697/figure/f3 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7583697/figure/...