Britain starts first coronavirus vaccines 70 hospitals in the U.K. have started administering Pfizer vaccine;…
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FDA approves drug for PET imaging of prostate cancer
(HealthDay)—The U.S. Food and Drug Administration approved the first drug for positron emission tomography (PET)…
View More FDA approves drug for PET imaging of prostate cancer
Moleculin Announces FDA Approves 3 Rare Pediatric Disease Designations for WP1066
HOUSTON, Dec. 1, 2020 /PRNewswire/ — Moleculin Biotech, Inc., (Nasdaq: MBRX) (Moleculin or the Company), a…
View More Moleculin Announces FDA Approves 3 Rare Pediatric Disease Designations for WP1066
Beware of coronavirus scams as vaccine approaches FDA approval: officials
Moderna to apply for emergency coronavirus vaccine approval HHS Secretary Alex Azar calls recent vaccine…
View More Beware of coronavirus scams as vaccine approaches FDA approval: officials
FDA clears Eli Lilly COVID-19 antibody treatment for emergency use
Why Pfizer’s ‘ultra-cold’ COVID-19 vaccine presents logistical challenges Dr. Amesh Adalja discusses the risks and…
View More FDA clears Eli Lilly COVID-19 antibody treatment for emergency use
FDA Approves Inmazeb (atoltivimab, maftivimab and odesivimab-ebgn) Antibody Cocktail for Ebola (Zaire Ebolavirus)
TARRYTOWN, N.Y., Oct. 14, 2020 /PRNewswire/ — Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) announced today that…
View More FDA Approves Inmazeb (atoltivimab, maftivimab and odesivimab-ebgn) Antibody Cocktail for Ebola (Zaire Ebolavirus)
FDA Approves Opdivo (nivolumab) + Yervoy (ipilimumab) as the First and Only Immunotherapy Treatment for Previously Untreated Unresectable Malignant Pleural Mesothelioma
PRINCETON, N.J.–(BUSINESS WIRE) October 2, 2020 — Bristol Myers Squibb (NYSE: BMY) today announced that…
View More FDA Approves Opdivo (nivolumab) + Yervoy (ipilimumab) as the First and Only Immunotherapy Treatment for Previously Untreated Unresectable Malignant Pleural Mesothelioma
FDA allows wide use of plasma for COVID-19 with little data that it works
Last week, the U.S. Food and Drug Administration (FDA) announced that it would not allow…
View More FDA allows wide use of plasma for COVID-19 with little data that it works
FDA approves first contact lens that slows myopia progression
(HealthDay)—MiSight, the first contact lens indicated to slow the progression of myopia in children ages…
View More FDA approves first contact lens that slows myopia progression
FDA: blood clot, death risk up with higher dose of tofacitinib
New warnings about an increased risk of thrombosis and of death among ulcerative colitis patients…
View More FDA: blood clot, death risk up with higher dose of tofacitinib