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RSS FeedPosted by Michael Wonder on 08 Apr 2016
FDA advisory committee unanimously recommends accelerated approval of Ocaliva (obeticholic acid) for the treatment of PBC
7 April 2016 - Intercept Pharmaceuticals today announced that the U.S. FDA's Gastrointestinal Drugs Advisory Committee voted 17 to 0 to ...
Posted by Michael Wonder on 05 Apr 2016
FDA approves Inflectra, a biosimilar to Remicade
5 April 2016 - The U.S. FDA today approved Inflectra (infliximab-dyyb) for multiple indications. Inflectra is administered by intravenous infusion. This ...
Posted by Michael Wonder on 05 Apr 2016
U.S. Food and Drug Administration approves Descovy (emtricitabine, tenofovir alafenamide), Gilead’s third TAF-based HIV therapy
4 April 2016 - Gilead Sciences, Inc. today announced that the U.S. FDA has approved Descovy (emtricitabine 200 mg/tenofovir alafenamide 25 ...
Posted by Michael Wonder on 01 Apr 2016
Dynavax announces FDA acceptance for review of biologics license application and PDUFA action date for Heplisav-B
30 March 2016 - Dynavax Technologies Corporation announced today that the U.S. FDA has accepted for review the biologics license application ...
Posted by Michael Wonder on 01 Apr 2016
FDA's view on biosimilar product labeling
31 March 2016 - To address biosimilar labeling in particular, the FDA has issued detailed recommendations to industry in the “Labeling ...
Posted by Michael Wonder on 30 Mar 2016
Newron receives complete response letter from US FDA for Xadago (safinamide mesylate)
29 March 2016 - Newron Pharmaceuticals and US WorldMeds announced today that a complete response letter from the FDA has been ...
Posted by Michael Wonder on 30 Mar 2016
OPKO Health receives complete response letter from FDA for Rayaldee new drug application
30 March 2016 - OPKO Health announces that the U.S. FDA has issued a complete response letter (CRL) to the company's ...
Posted by Michael Wonder on 30 Mar 2016
FDA approves first treatment for rare disease in patients who receive stem cell transplant from blood or bone marrow
30 March 2016 - The U.S. FDA today approved Defitelio (defibrotide sodium) to treat adults and children who develop hepatic veno-occlusive ...
Posted by Michael Wonder on 30 Mar 2016
Additional dosage strengths of Otrexup (methotrexate) injection approved by FDA
29 March 2016 - Antares Pharma today announced the approval by the U.S. Food and Drug Administration (FDA) of three ...
Posted by Michael Wonder on 29 Mar 2016
Lundbeck and Takeda receive complete response letter by the FDA for Brintellix (vortioxetine hydrobromide) sNDA
29 March 2016 - Takeda and Lundbeck today announced that the U.S. FDA has issued a complete response letter (CRL) for ...
Posted by Michael Wonder on 25 Mar 2016
FDA takes important step to increase the development of, and access to, abuse-deterrent opioids
24 March 2016 - The U.S. Food and Drug Administration today issued a draft guidance intended to support industry in their ...
Posted by Michael Wonder on 23 Mar 2016
FDA approves Cinqair to treat severe asthma
23 March 2016 - The U.S. Food and Drug Administration today approved Cinqair (reslizumab) for use with other asthma medicines for ...
Posted by Michael Wonder on 22 Mar 2016
FDA approves new psoriasis drug Taltz (ixekizumab)
22 March 2016 - The U.S. Food and Drug Administration today approved Taltz (ixekizumab) to treat adults with moderate-to-severe plaque psoriasis. ...
Posted by Michael Wonder on 21 Mar 2016
FDA approves new treatment for inhalation anthrax
21 March 2016 - The U.S. FDA has approved Anthim (obiltoxaximab) injection to treat inhalational anthrax in combination with appropriate ...
Posted by Michael Wonder on 19 Mar 2016
Eagle Pharmaceuticals receives complete response letter from FDA on Kangio (bivalirudin) application
18 March 2016 - Eagle Pharmaceuticals, today announced that it has received a Complete Response Letter from the U.S. FDA for ...