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BioWorld - Friday, January 30, 2026
Home » Topics » Regulatory » EMA

EMA
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Biovest's BiovaxID receives E.U. orphan drug status in mantle cell lymphoma

March 10, 2011

Pfizer's axitinib receives European orphan drug status in renal cell carcinoma

March 10, 2011

EMA accepts Insmed's pediatric investigation plan for Arikace

March 9, 2011

European orphan drug status for Talecris' human plasmin in acute peripheral arterial occlusion

March 9, 2011

Vical and EMA reach agreement on endpoints for pivotal phase III trial of TransVax vaccine

March 8, 2011

Rare Disease Day / Recently launched orphan drugs

Feb. 28, 2011

Sanofi-aventis profiles progress of fourth quarter 2010

Feb. 28, 2011

CHMP recommends change to Humira indication

Feb. 22, 2011

EMA committee recommends approval of Sprimeo HCT for hypertension

Feb. 22, 2011

Prima BioMed receives scientific advice from EMA on CVac trial

Feb. 22, 2011
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