The latest drug development news and highlights from our US FDA Performance Tracker.
Here's your US review and approval news for the week in brief: Three more companies picked up breakthrough therapy designations this week – Alnylam Pharmaceuticals Inc., Proteostasis Therapeutics Inc. and Janssen Pharmaceutical Cos. – in what continues to be a busy year for the expedited pathway.
Merck & Co. Inc.'s PD-1 inhibitor Keytruda (pembrolizumab) scored a priority review for a cervical cancer indication, putting the...
<p>Executive Summary</p> <p>A list of EU biosimilar filings, CHMP opinions and EU marketing authorizations, including details of the biosimilar company, the brand name/INN, indication(s), the reference product/company, and the date and type of event.</p>
Cardiovascular and Renal Drugs Advisory Committee will consider whether open-label extension data from a randomized trial that failed its primary endpoint, along with a historical control comparison, are enough to support approval in the ultra-rare disease.
<p>Executive Summary<p> <p>The Pink Sheet's list of EU centralized approvals of new active substances has been updated to add six new products, incl/ding Ixchiq, Valneva's chikungunya virus vaccine</p>
Revised recommendation is based on most recent data on circulating strains in US, where KP.3 is now dominant. Novavax sticks with plans targeting the JN.1 ‘parent strain.’
Pink Sheet reporter and editors discuss the US FDA’s changes to the COVID-19 vaccine indication and its revocation of the vaccine emergency use authorizations, as well as new vaccine coverage and reimbursement questions.
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