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.
Bixlenvo is a once-daily single tablet HIV treatment for virologically-suppressed adults.
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Available in tablets for oral use and oral suspension, Tivicay PD is the first of its kind available to pediatric patients.
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The expansion creates commercial-scale batch tablet capacity by bringing spray drying and tableting to the same site.
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The once daily tablets reduced the risk of death by 60% compared to chemotherapy.
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Just weeks after getting the FDA green light, Japan’s Ministry of Health, Labor and Welfare has approved Takeda’s Ozeful tablets.
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The drug is currently only available through private healthcare and not via the publicly-funded NHS.
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If approved, the drug will be the first new treatment for pediatric patients with Tourette syndrome in 10 years.
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If confirmed by the Senate, the White House domestic policy aide would replace former FDA chief Marty Makary.
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The first of its kind for hypophosphastasia, the orally-active drug is currently undergoing a phase 1/2a trial.
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If approved, DT120 ODT could offer a treatment option that works through an entirely different mechanism than anything currently used in clinical practice.
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Zenbexus marks the arrival of a new treatment class.
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The deal will give the company a potential first-in-class oral drug for rare form epilepsy.
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The experimental small molecule failed to meet the key activity endpoint in a phase 2a trial.
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The oral orexin receptor 2 agonist treats the orexin deficiency that leads to NT1.
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If approved, gildeuretinol will be the first FDA-approved therapy for the inherited retinal disease.
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