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2019
Pharma News, 2019
FDA flags risks from AbbVie, Gilead, Merck hepatitis C drugs to certain patients
(Reuters) - The U.
U.S. judge rules for Regeneron, Sanofi in Amgen cholesterol drug patent fight
(Reuters) - A U.
FDA Approves Ixekizumab for Ankylosing Spondylitis Indication
Officials with the FDA have approved Eli Lilly’s ixekizumab (Taltz) injection 80 mg/mL for the treatment of active ankylosing spondylitis (AS), also known as radiographic axial spond...
OxyContin maker negotiating settlement worth a reported $12B
Purdue Pharma and the thousands of state and local governments suing the maker of OxyContin over the nation's deadly opioid crisis are negotiating a $10 billion to $12 billion settlement under whi...
Lilly’s atopic dermatitis drug hits endpoints
Eli Lilly and Incyte have announced that Olumiant (baricitinib) met the primary endpoint in BREEZE-AD7, the third pivotal Phase III trial in the BREEZE-AD program to be completed in 2019.
Amgen to buy Celgene’s Otezla in $13.4bn deal
Amgen agreed to buy Celgene’s Otezla, a treatment for psoriasis and Behçet’s disease, for $13.
Roche's personalized cancer treatment wins FDA approval
(Reuters) - The U.
FDA Approves Wakix
PLYMOUTH MEETING, PA, — Harmony Biosciences, LLC (Harmony) announced today that the U.
Sarepta stumbles on FDA rejection of a new drug to treat Duchenne muscular dystrophy
Sarepta Therapeutics was dealt a surprising setback Monday when the Food and Drug Administration rejected its marketing application for a second drug that aimed to treat children with Duchenne muscula...
FDA Approves Fedratinib for the Treatment of Myelofibrosis
On August 16, 2019, the Food and Drug Administration approved fedratinib (INREBIC, Impact Biomedicines, Inc.
Fatality in Phase I Clinical Study of E2082
TOKYO, Japan I July 30, 2019 I Eisai Co.
FDA Approves Bayer’s Nubeqa® (darolutamide), a New Treatment for Men with Non-Metastatic Castration-Resistant Prostate Cancer
WHIPPANY, N.
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