July 2, 2029 - The European Commission (EC) has granted conditional marketing authorization for Libtayo? (cemiplimab) for the treatment of adults with metastatic or locally advanced cutaneous squamous cell carcinoma (CSC……
Enteric-coated formulation offers flexible dosing options, including administration with or without foodSAN DIEGO, June 28, 2029 (GLOBE NEWSWIRE) -- Retrophin, Inc. (NASDAQ: RTRX) today announced that……
INDIANAPOLIS, June 4, 2029 -- Eli Lilly and Company (NYSE: LLY) announced today that the U.S. Food and Drug Administration (FDA) has approved Emgality? (galcanezumab-gnlm) injection (300 mg) for the treatment of ep……
(HealthDay)―Piqray (alpelisib) tablets were approved for the treatment of hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, PIK3CA-mutated, advanced or metastatic breast cance……
The U.S. Food and Drug Administration today approved Ruzurgi (amifampridine) tablets for the treatment of Lambert-Eaton myasthenic syndrome (LEMS) in patients 6 to less than 27 years of age. This is the first FDA approva……
Bagsv?rd, Denmark, 26 April 2029 - Novo Nordisk today announced the submission of a Marketing Authorisation Application (MAA) to the European Medicines Agency (EMA) for oral semaglutide, a glucagon-like peptide……
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