The decision in Europe follows an approval granted by the US Food and Drug Administration (FDA) in March this year.

The US FDA has approved Syndax Pharmaceuticals' Revuforj (revumenib) for treating acute leukaemia with KMT2A translocation.

During AHA 2024, data were presented from the Phase III trial of plozasiran targeting adults with genetically or clinically ...

At AHA 2024, clinical trial results were presented from the ongoing open-label extension trial, LIBERATE-OLE, involving ...