Aptinyx receives FDA fast track designation for development of NYX-2925 as treatment for neuropathic pain associated with diabetic peripheral neuropathy

13 September 2016 - Data from pre-clinical investigation of NYX-2925 to be presented at 16th World Congress on Pain on ...

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Tesaro receives FDA fast track designation for niraparib and initiates rolling NDA submission

12 September 2016 - Tesaro today announced that the U.S. FDA has granted fast track designation to niraparib for the treatment ...

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Sage receives FDA breakthrough therapy designation for SAGE-547 for the treatment of postpartum depression

6 September 2016 - Designation offers potential for expedited development and review, and underscores significant unmet need in women with postpartum ...

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FDA accepts supplemental biologics license application, assigns priority review and grants breakthrough therapy designation to Merck’s Keytruda (pembrolizumab) for first-line treatment of patients with advanced non-small-cell lung cancer

7 September 2016 - Merck has also submitted a marketing authorization application to the EMA for Keytruda in the same patient ...

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FDA approves Blincyto (blinatumomab) for use In paediatric patients with Philadelphia chromosome negative relapsed or refractory B-cell precursor acute lymphoblastic leukemia

1 September 2016 - Amgen today announced that the U.S. FDA has approved the supplemental biologics license application for Blincyto (blinatumomab) ...

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Biogen’s investigational Alzheimer’s disease treatment aducanumab granted FDA fast track designation

1 September 2016 - Company also provides update on new interim analysis from phase 1b study. ...

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FDA accepts Mitsubishi Tanabe Pharma’s NDA filing for edaravone to treat ALS

30 August 2016 - Edaravone may be the first ALS treatment approved in U.S. in more than 20 years. ...

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ARIAD completes rolling submission of new drug application for brigatinib to the U.S. FDA

30 August 2016 - ARIAD Pharmaceuticals today announced it has completed the rolling submission of the new drug application for its ...

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Genmab announces U.S. FDA approval of Arzerra (ofatumumab) in combination with fludarabine and cyclophosphamide for relapsed CLL

31 August 2016 - Arzerra now approved by U.S. FDA for use in combination with fludarabine and cyclophosphamide in relapsed CLL ...

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Neurocrine submits new drug application for valbenazine for treatment of tardive dyskinesia

29 August 2016 - Neurocrine Biosciences today announced that it has submitted a new drug application to the U.S. FDA for ...

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FDA approves Sandoz Erelzi to treat multiple inflammatory diseases

30 August 2016 - Erelzi is the first biosimilar etanercept approved by the FDA, offering expanded access to this important medicine. ...

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Cynapsus Therapeutics receives FDA fast track designation for APL-130277 for the treatment of off episodes in patients with Parkinson’s disease

29 August 2016 - Cynapsus Therapeutics today announced that the U.S. FDA has granted fast track designation for APL-130277, a product ...

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Amgen's shameful silence covers up reasons for FDA drug rejection

25 August 2016 - An Amgen drug to treat secondary hyperparathyroidism was rejected by U.S. FDA  but the company has offered ...

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Mallinckrodt receives FDA fast track designation for Synacthen Depot IND application

25 August 2016 - Expedites potential treatment for Duchenne muscular dystrophy. ...

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PhRMA and BIO give support for PDUFA VI performance goals

24 August 2016 - Both PhRMA and BIO have said they are pleased with the performance goals outlined by and ...

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