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BioWorld - Friday, February 27, 2026
Home » Topics » Regulatory » EMA

EMA
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Adaptimmune Therapeutics gains access to EMA's PRIME initiative for T-cell therapy

July 29, 2016

Omeros receives scientific advice from EMA on phase III program for OMS-721

July 29, 2016

EMA grants PRIME designation to DNX-2401 for recurrent glioblastoma

July 28, 2016

Ebola Zaire vaccine wins FDA breakthrough therapy designation and PRIME status

July 26, 2016

EMA's CHMP adopts positive opinion on type II variation application for Gilead's Truvada

July 25, 2016

EMA committee supports approval of Eisai's Kisplyx

July 25, 2016

EMA's CHMP grants positive opinion to Cabometyx in RCC

July 25, 2016

EMA committee recommends approval of Onivyde in E.U.

July 25, 2016

EMA proposes changes to guidance on first-in-human trials

July 22, 2016

EMA grants orphan drug designation to XOMA-358

July 21, 2016
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