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RSS FeedPosted by Michael Wonder on 15 Sep 2015
Erytech submits EMA marketing authorisation application for Graspa to treat acute lymphoblastic leukaemia
14 September 2015 - Erytech Pharma, the French biopharmaceutical company that develops innovative ‘tumor starvation’ treatments for acute leukemia and other ...
Posted by Michael Wonder on 11 Sep 2015
Amgen submits application to FDA for new delivery option for monthly administration of Repatha (evolocumab)
11 September 2015 - Amgen today announced the submission of an application to the U.S. Food and Drug Administration (FDA) seeking ...
Posted by Michael Wonder on 11 Sep 2015
AbbVie's Humira (adalimumab) receives U.S. FDA approval for moderate to severe hidradenitis suppurativa
10 September 2015 - AbbVie, a global biopharmaceutical company, today announced that the U.S. Food and Drug Administration (FDA) approved Humira ...
Posted by Michael Wonder on 10 Sep 2015
U.S. FDA accepts first digital medicine new drug application for Otsuka and Proteus Digital Health
10 September 2015 - Otsuka Pharmaceutical Co., Ltd. and Proteus Digital Health today announced that the United States Food and Drug ...
Posted by Michael Wonder on 10 Sep 2015
FDA grants fast track designation for MediciNova's MN-001 (tipelukast) for the treatment of idiopathic pulmonary fibrosis
10 September 2015 - MediciNova, Inc., a biopharmaceutical company traded on the NASDAQ Global Market and the JASDAQ Market of the ...
Posted by Michael Wonder on 09 Sep 2015
U.S. FDA grants priority review to Takeda's ixazomib citrate for patients with relapsed/refractory multiple myeloma
9 September 2015 - Takeda Pharmaceutical Company Limited today announced that the U.S. Food and Drug Administration (FDA) has granted priority ...
Posted by Michael Wonder on 09 Sep 2015
FDA grants Genentech’s alectinib priority review for specific type of ALK-positive lung cancer
9 September 2015 - Genentech, a member of the Roche Group, announced today that the U.S. Food and Drug Administration (FDA) ...
Posted by Michael Wonder on 04 Sep 2015
Alexion receives notification of PDUFA date extension for Kanuma (sebelipase alfa)
4 September 2015 - Alexion Pharmaceuticals, Inc. announced today that the U.S. Food and Drug Administration (FDA) has extended the Prescription ...
Posted by Michael Wonder on 04 Sep 2015
US FDA grants breakthrough therapy designation for Roche’s investigational medicine ACE910 for people with haemophilia A with factor VIII inhibitors
4 September 2015 - Roche today announced that the US Food and Drug Administration (FDA) has granted breakthrough therapy designation to ...
Posted by Michael Wonder on 04 Sep 2015
US FDA approves expanded indication for Brilinta to include long-term use in patients with a history of heart attack
3 September 2015 - AstraZeneca today announced that the US Food and Drug Administration (FDA) has approved Brilinta (ticagrelor) tablets at ...
Posted by Michael Wonder on 03 Sep 2015
Acadia Pharmaceuticals submits new drug application for Nuplazid for the treatment of Parkinson’s disease psychosis
3 September 2015 - Acadia Pharmaceuticals Inc., a biopharmaceutical company focused on the development and commercialisation of innovative medicines to address ...
Posted by Michael Wonder on 03 Sep 2015
U.S. FDA approves update of Simponi Aria (golimumab for infusion) label to include improvement in both physical and emotional measures of health when treating moderately to severely active rheumatoid arthritis
4 September 2015 - Janssen Biotech, Inc. announced today the approval of a U.S. Food and Drug Administration (FDA) Supplemental ...
Posted by Michael Wonder on 03 Sep 2015
Novartis launches first U.S. 'biosimilar' drug at 15 percent discount
3 September 2015 - Novartis kicked off a new era in U.S. medicine on Thursday with the launch of the first ...
Posted by Michael Wonder on 03 Sep 2015
Sandoz launches Zarxio (filgrastim-sndz), the first biosimilar in the United States
3 September 2015 - Sandoz, a Novartis company, announced today that Zarxio (filgrastim-sndz) is now available in the United States. Zarxio ...
Posted by Michael Wonder on 02 Sep 2015
Allergan announces FDA approval of updated label for Teflaro (ceftaroline fosamil)
2 September 2015 - Allergan plc. today announced the U.S. Food and Drug Administration (FDA) has approved the company's supplemental new ...