The latest news from the global pharmaceutical industry. Below you will find news and information to keep you up-to-date with what is happening in your industry. Coverage includes regulatory approvals, recall announcements, mergers and acquisitions, personnel news and appointments, new facility and facility expansion updates, collaborations and agreements, and financial updates.
Monday, February 12, 2018
Alkahest has been awarded a grant from The Michael J. Fox Foundation for Parkinson's Research (MJFF) to support a Clinical Trial of GRF6019.
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Friday, February 09, 2018
BI 409306 was investigated in two studies (NCT 02240693 and NCT 02337907), designed to show superiority of BI 409306 over placebo in cognition. ...
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Friday, February 09, 2018
Teva announced the launch of generic version of Syprine (trientine hydrochloride) capsules, 250 mg, in the U.S.
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Wednesday, February 07, 2018
Bristol-Myers Squibb announced the ongoing Phase 3 study met its co-primary endpoint of PFS with the Opdivo plus Yervoy combination in first-line ...
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Tuesday, February 06, 2018
Treatment with the combination of encorafenib and binimetinib reduced the risk of death compared to treatment with vemurafenib.
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Monday, February 05, 2018
Trethera announced the FDA has cleared its IND application for TRE-515, a novel, first-in-class inhibitor of deoxycytidine kinase for the treatment of...
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Thursday, February 01, 2018
Imago BioSciences announced the FDA has accepted their IND application providing clearance to proceed with the clinical development of IMG-7289 in the...
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Tuesday, January 30, 2018
Dauntless Pharmaceuticals has granted orphan drug designation to DP1038.
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Takeda announced that the FDA has granted Fast Track designation to TAK-426, Takeda’s purified, inactivated, alum-adjuvanted, whole Zika virus vaccine...
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Theravance Biopharma and Mylan announced the FDA has accepted for review the companies' recently submitted NDA for revefenacin (TD-4208).
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GlaxoSmithKline Pharmaceuticals
GlaxoSmithKline and Innoviva announced the EMA’s CHMP has issued a positive opinion recommending a label update for the use of once-daily Relvar ...
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The FDA approved Lutathera for the treatment of a type of cancer that affects the pancreas or gastrointestinal tract called GEP-NET.
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Wednesday, January 24, 2018
BioAtla announced the U.S. Food and Drug Administration (FDA) has cleared BioAtla's Investigational New Drug application (IND) for BA3011.
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Tuesday, January 23, 2018
ProMIS has announce its lead product candidate for Alzheimer's disease, PMN310, showed significantly greater binding to the neurotoxic oligomer-...
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Tuesday, January 23, 2018
Swedish Orphan Biovitrum AB announced the FDA has accepted the IND application for the drug candidate SOBI003.
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