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BioWorld - Tuesday, January 13, 2026
Home » Topics » Regulatory » EMA

EMA
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Lux Biosciences withdraws Luveniq MAA

Oct. 19, 2011

EMA confirms design of Intercell's planned phase II/III trial of Pseudomonas aeruginosa vaccine

Oct. 13, 2011

EMA recommends new orphan designation for 4SC-201

Oct. 13, 2011

EMA accepts MAA for IB-1001

Oct. 4, 2011

Aegerion gives update on European filing for lomitapide

Sep. 30, 2011

CHMP recommends approval of Prevanar 13 for new indication

Sep. 28, 2011

CHMP issues opinion on new indication for Avastin

Sep. 28, 2011

CHMP recommends approval of Alimta for new indication

Sep. 27, 2011

FDA approves new indication for Soliris

Sep. 27, 2011

Kombiglyze recommended for approval in E.U.

Sep. 27, 2011
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