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Molnupiravir FDA Approval Status
Molnupiravir (EIDD-2801/MK-4482) is an investigational, orally bioavailable form of a potent ribonucleoside analog in development for the treatment of COVID-19.1.Molnupiravir works as an antiviral agent by inhibiting the replication of the SARS-CoV-2 virus, th..
2021-10-25
COVID-19 tracker: Azar pegs 6.4M Pfizer doses for mid-December delivery; GAVI welcomes AZ shot data
The U.S. expects to distribute 6.4 million doses of Pfizer and BioNTech's shot by mid-December, should the vaccine pass the FDA's bar, Department of Health and Human Services secretary Alex Azar said. Meanwhile, the World Health Organization's vacc..
2020-11-26
Pfizer urged to hold off on coronavirus vaccine until late November: report
Pfizer CEO Albert Bourla and his vaccine partner BioNTech have said the companies expect phase 3 data by the end of October—and that an FDA application could soon follow. But more than 60 researchers and bioethicists urged the partners to wait for mor..
2020-09-29
Judge wipes out Biogen's Tecfidera patent protections in suit against Mylan
In the high-stakes patent fight between Biogen and Mylan over Tecfidera’s main remaining patent, Mylan has scored a major win in federal court.U.S. District Judge Irene Keeley said Mylan “demonstrated by clear and convincing evidence” that certain claims ..
2020-06-19
Takeda, debt in mind, offloads 18 drugs in Asia Pacific to Celltrion for $278M
Takeda has earmarked another chunk of business for divestment to help it pay down debt.The Japanese pharma is offloading 18 over-the-counter and prescription drugs marketed in the Asia-Pacific region to South Korea’s Celltrion for $278 million, it said on T..
2020-06-12
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