Provided By GlobeNewswire
Last update: May 8, 2025
– Receives regulatory authorization in the EU for ELEVATE-44-201, a Phase 1/2 MAD clinical study of ENTR-601-44 in patients living with Duchenne muscular dystrophy who are amenable to exon 44 skipping –
Read more at globenewswire.comNASDAQ:TRDA (12/19/2025, 2:53:06 PM)
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