Just two weeks after Biogen completed its buyout of Reata Pharmaceuticals, the combined company is trimming its staff.
Reata Pharmaceuticals Stockholders Approve Merger Transaction With Biogen Inc.
Biogen’s $7.3 billion buyout of Skyclarys-maker Reata Pharmaceuticals surprised some industry watchers last month. But it turns out Biogen wasn’t the only drugmaker jockeying for the Texas-based rare disease outfit, a new securities filing shows.
Biogen said it would buy biotech firm Reata Pharmaceuticals for roughly $6.5 .. nnnRead more at: nhttps://health.economictimes.indiatimes.com/news/pharma/biogen-to-buy-reata-for-6-5-bln-to-bulk-up-rare-disease-portfolio/102220586
SKYCLARYS® recently approved in US as the only treatment indicated for patients with Friedreich™s ataxia Proposed acquisition represents meaningful step forward in Biogen™s strategy for...
Plano-based Reata Pharmaceuticals announced Tuesday that Skyclarys, the first Food and Drug Administration-approved treatment for the ultra-rare neuromuscular disease Friedreich’s ataxia, is now available to patients.
PLANO, Texas--(BUSINESS WIRE)--Reata Pharmaceuticals, Inc. (Nasdaq: RETA) (“Reata,” the “Company,” “our,” “us,” or “we”), a global, biopharmaceutical company focused on developing and commercializing novel therapies for patients with severe diseases, announced that the United States Food and Drug Administration (FDA) has approved the Prior Approval Supplement (PAS) to update the drug substance specification for SKYCLARYS® (omaveloxolone), the first and only FDA approved drug for the treatment of Friedreich’s ataxia in adults and adolescents aged 16 years and older. With the approval of the PAS, SKYCLARYS is now available to patients with Friedreich’s ataxia in the United States.
PLANO, Texas--(BUSINESS WIRE)--Reata Pharmaceuticals, Inc. (Nasdaq: RETA) (“Reata,” the “Company,” “our,” “us,” or “we”), a global biopharmaceutical company focused on developing and commercializing novel therapies for patients with severe diseases, announced today that the U.S. Food and Drug Adistration (FDA) accepted for filing the Prior Approval Supplement (PAS) to update the drug substance specification for SKYCLARYS® (omaveloxolone). As per the US Code of Federal Regulation, the filing means FDA has made a threshold deteration that the PAS is sufficiently complete to permit a substantive review. As previously communicated, the PAS is being reviewed under expedited Priority Review with a target action date of mid-August 2023.
PLANO, Texas--(BUSINESS WIRE)--Reata Pharmaceuticals, Inc. (Nasdaq: RETA) (“Reata,” the “Company,” “our,” “us,” or “we”), a global biopharmaceutical company focused on developing and commercializing novel therapies for patients with severe diseases, announced the appointment of Rajiv Patni, M.D., as Executive Vice President, and Chief Research & Development Officer. Dr. Patni will report to Warren Huff, Chief Executive Officer, and will be responsible for overseeing the Company’s research and development functions.
PLANO, Texas--(BUSINESS WIRE)--Reata Pharmaceuticals, Inc. (Nasdaq: RETA) (“Reata,” the “Company,” “our,” “us,” or “we”), a global biopharmaceutical company focused on developing and commercializing novel therapies for patients with severe diseases, announced that management will participate in the Goldman Sachs 44th Annual Global Healthcare Conference on June 12 – 15, 2023, in Dana Point, California. Manmeet Soni, Reata’s President, Chief Operating Officer, and Chief Financial Officer will be participating in a fireside chat during the conference.