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.
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This is the company’s third positive phase 3 readout for its DT120 orally disintegrating tablet.
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Etcamah didn't meet the primary endpoint of progression-free survival in patients with ER-positive, HER2-negative advanced breast cancer.
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The rebrand comes as Novo Nordisk races to close the gap with obesity-drug rival Eli Lilly.
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The first prophylactic for all three types of HAE, the drug reduced attack rates by 83%.
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Etcamah in combination with a CDK4/6 inhibitor reduced the risk of disease progression or death by 56% versus standard-of-care treatment.
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AstraZeneca plans to launch Zegfrovy in the U.S. during the fourth quarter of 2026.
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The BTK inhibitor met its primary and key secondary endpoints, while also demonstrating a favorable safety profile.
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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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