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.
Lipfendra reduced LDL-C by more than 50%, including in patients with HeFH.
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The deal gives Lilly a pipeline of rapid-acting neuroplastogens.
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The tablets were granted accelerated approval in China and U.S. for locally advanced/metastatic NSCLC with EGFR exon20ins.
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The partners have received a third CRL for their rivoceranib-camrelizumab combo in hepatocellular carcinoma.
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The selective TLR 7/8 inhibitor could become the first approved therapy for cutaneous manifestations of lupus.
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The company used AI to prioritize the novel target as well as to generate and optimize the small molecule.
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The orally-available compound could provide an alternative to conventional glucocorticoids, the current standard of care.
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A rolling NDA submission for treatment-resistant depression with the FDA is underway.
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If approved, deucrictibant will be the first oral bradykinin B2 receptor antagonist to treat HAE attacks.
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Vertex will pick up an FDA-approved oral therapy for acromegaly and a phase 3 drug to treat CAH.
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The phase 1/2 study will evaluate the combo in EGFR-mutated and PD-L1 positive locally advanced or metastatic NSCLC.
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The retraction comes amid increasing regulatory scrutiny of the drug.
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Centanafadine was granted Priority Review and has a PDUFA target action date of July 24, 2026.
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The company is adding leading brands to its portfolio to boost its position in Belgium, Poland, and the Nordics.
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The phase 1b/2 trial will be the first time that an eIF2B is administered to people with VWM disease.
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