The U.S. government will run out of supplies of COVID-19 treatments known as monoclonal antibodies as soon as late May and will have to scale back plans to get more unless Congress provides more funding, the White House said on March 15.
The U.S. Food and Drug Administration revised the emergency use authorization (EUA) for AstraZeneca’s Evusheld to a higher dose to be effective in the prevention of COVID-19.
WHO Tracking 4 Omicron Subvariants while a New Antibody Gets the Nod
Antivirals, Bebtelovimab (LY-CoV1404; LY3853113), BNT162b2 (Pfizer and BioNTech), CDC, Congress, Coronavirus Disease (COVID-19) Pandemic, COVID-19 Antibodies, COVID-19 booster shots, COVID-19 protocols, COVID-19 shots, COVID-19 Vaccines, Covid-19 Variants, Eli Lilly, Emergency Use Authorization (EUA), FDA, Immunocompromised, JAMA Network, Janssen COVID-19 Vaccine (J&J), Joe Biden, Johnson & Johnson, Mask-wearing, Molnupiravir, mRNA-1273/Moderna COVID-19 Vaccine (Moderna), Omicron (B.1.1.529) (South Africa), Omicron BA.2, Paxlovid, Public Health Emergencies, R&D, Surgeon general, WHO, World Health OrganizationThe World Health Organization indicated WHO is tracking four Omicron subvariants: BA.1, BA.1.1, BA.2 and BA.3. BA.2 has a growth advantage over BA.1, the variant responsible for the recent Omicron surge.
Eli Lilly and Co. entered an agreement with the U.S. government to supply up to 600,000 doses of the company’s developmental COVID-19 antibody drug for at least $720 million.
GSK sees sales growth in 2022 after quarterly beat, prepares for spin-off
Business, Clinical Trials, Consumer Healthcare, Coronavirus Disease (COVID-19) Pandemic, COVID-19 Antibodies, Deals, Forecasts, Gilead, GlaxoSmithKline, Quarterly results, R&D, Respiratory Syncytial Virus (RSV) Infection, Settlements, Shingles, Therapeutics, Vaccines, Vir BiotechnologyBritain’s GSK forecast growth in 2022 after racking up 1.4 billion pounds ($1.9 billion) in COVID-related sales in 2021, beating quarterly forecasts in the company’s first earnings report since rejecting Unilever’s bid for GlaxoSmithKline’s consumer arm.
Companies Making the Biggest Bucks from COVID-19 Therapeutics Sales
Analysts, Antivirals, Bamlanivimab (LY-CoV555), Biopharma Companies, Business, Coronavirus Disease 2019 (COVID-19), COVID-19 Antibodies, COVID-19 Therapeutic, Deals, Eli Lilly, Etesevimab (Lilly), Gilead, Investors, Merck, Molnupiravir, Omicron (B.1.1.529) (South Africa), Paxlovid, Pfizer, REGEN-COV (casirivimab and imdevimab), Regeneron Pharmaceuticals, Remdesivir, Sales, Therapeutics, U.S. governmentAlthough the COVID-19 pandemic has hit companies unevenly, some biopharma firms that have produced new drugs or vaccines against the disease have shown big spikes in drug sales. BioSpace reviewed five companies that produced non-vaccine treatments for COVID-19.
About 35% of People Who Received Placebo in Vaccine Trials Report Side Effects and More COVID-19 News
Adverse Events, BNT162b2 (Pfizer and BioNTech), Business, CDC, Clinical Trials, COVID-19 Antibodies, COVID-19 forecasts, COVID-19 Studies, COVID-19 Vaccines, Harvard Medical School, Intensive Care Units (ICUs), JAMA, Janssen COVID-19 Vaccine (J&J), Johnson & Johnson, Long COVID, mRNA-1273/Moderna COVID-19 Vaccine (Moderna), Nature Communications, Omicron (B.1.1.529) (South Africa), Placebo, R&D, Side Effects, The NetherlandsAccording to a recent study conducted by researchers at Harvard Medical School and Beth Israel Deaconess Medical Center, 76 percent of the adverse side effects (such as fatigue or headache) that people experienced after receiving their first COVID-19 vaccination were also reported by participants who received a placebo shot.
Pfizer Inc. and BioNTech SE said on Jan. 25 they started a clinical trial to test a new version of their vaccine specifically designed to target the COVID-19 Omicron variant, which has eluded some of the protection provided by the original two-dose vaccine regimen.
U.S. FDA limits use of Regeneron, Lilly COVID-19 antibody treatments
Antivirals, Clinical Data, COVID-19 Antibodies, COVID-19 Therapeutics, Eli Lilly, Emergency Use Authorization (EUA), Gilead, Monoclonal Antibodies, Omicron (B.1.1.529) (South Africa), Regeneron Pharmaceuticals, Remdesivir, TherapeuticsThe U.S. health regulator revised on Jan. 24 the emergency use authorizations for COVID-19 antibody treatments from Regeneron and Eli Lilly to limit their use, as the drugs are unlikely to work against the Omicron coronavirus variant.
GlaxoSmithKline and U.S. partner Vir Biotechnology will boost production of their antibody-based COVID-19 treatment by adding a second manufacturing plant to help meet soaring demand in the United States.