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Keeping Track: US Approvals For Xpovio And Xembify Highlight Short Holiday Week

 
• By Michael Cipriano

The latest drug development news and highlights from our US FDA Performance Tracker.

Keeping Track Feature image

The US Food and Drug Administration largely cleared out its desk in advance of the Fourth of July celebration, although the agency still approved two novel products during the short holiday week inKaryopharm Therapeutics Inc.'s Xpovio (selinexor) and Grifols SA's Xembify (immune globulin subcutaneous, human- klhw).

Biohaven Pharmaceutical Holding Co. Ltd. announced a submission for its novel acute migraine treatment rimegepant, while Puma Biotechnology Inc

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Blenrep’s Revival Gains Steam: EMA Decision Imminent As Japan Approves New Regimen

 
• By Neena Brizmohun

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New EU Filings

 
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Blenrep’s Revival Gains Steam: EMA Decision Imminent As Japan Approves New Regimen

 
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Smoldering Myeloma Endpoint Questions Carry J&J’s Darzalex Faspro To US FDA AdComm

 
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US FDA Adcomm To Consider If Genentech’s Columvi Study Generalizable To US

 
• By Sue Sutter

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