Delivers up-to-date industry news on topics like drug approvals, product recalls, company expansions and acquisitions, market trends for all OSD forms, as well as excipients, packaging and supply chain issues. Monitors market trends in specific drug categories as well as in supplements/nutraceuticals. Provides updates on clinical trials. Includes alerts about new or upcoming regulatory issues.
India’s ACG has kicked off operations at its new 1.89 million-square-foot capsule manufacturing facility in Rayong, Thailand.
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Crenessity offers a breakthrough in the treatment landscape for classic CAH.
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Per the deal, Terray will utilize its tNova platform to discover and develop small molecule compounds against a set of targets selected by Gilead.
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The FDA has identified cases of serious liver injury among patients being treated for primary biliary cholangitis who did not have cirrhosis of the liver.
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AbbVie will pick up Nimble’s lead asset, a preclinical oral peptide IL23R inhibitor in development for the treatment of psoriasis.
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Lonza has unveiled a new organizational structure that focuses on its core CDMO services, which includes shedding its Capsules & Health Ingredients business.
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The phase 3 trial win for its D1/D5 partial agonist tees up AbbVie for an NDA submission in 2025.
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The generics giant has entered into an agreement with JKI to divest Teva-Takeda, its generics business venture in Japan.
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GSK has signed a research alliance with Danish biotech start-up Muna Therapeutics focused on novel drug targets for the treatment of Alzheimer’s.
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GSK has signed a multi-year, multi-target strategic research alliance with biotech start-up Rgenta Therapeutics.
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Novartis has signed a potential $2.9 billion agreement with PTC Therapeutics for its Huntington's disease program.
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The FDA has issued a CRL for govorestat, a novel, CNS-penetrant aldose reductase inhibitor for the treatment of the rare genetic metabolic disease.
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The FDA has extended the review period for Soleno's DCCR tablets for the treatment of Prader-Willi syndrome, pushing the PDUFA date to March.
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PTC's oral small molecule, utreloxastat, failed to meet its primary endpoint of slowing disease progression in ALS in a global phase 2 study.
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Simufilam, which has been plagued with controversy for years, proved no better than placebo in the ReThink-ALZ study.
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