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Committee for Medicinal Products for Human Use

European Commission revokes marketing authorisation for Novartis’ crizanlizumab

11 August 2023 | By Caroline Peachey (European Pharmaceutical Review)

Novartis will remove its sickle cell medicine crizanlizumab from the EU/EEA market following a European Commission decision.

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CHMP recommends Pluvicto^® for treating advanced prostate cancer

17 October 2022 | By Izzy Wood (European Pharmaceutical Review)

CHMP issues positive opinion on Pluvicto®, paving the way for it to become the first European-approved radioligand therapy for metastatic prostate cancer patients.

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Proposed biosimilar accepted for review by EMA

3 June 2019 | By Victoria Rees (European Pharmaceutical Review)

The EMA has accepted Prestige BioPharma’s marketing application for its trastuzumab biosimilar.

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EMA grants marketing authorisation for Prevymis against cytomegalovirus

10 November 2017 | By

The EMA has recommended granting a marketing authorisation Prevymis, an antiviral medicine that prevents CMV reactivation and disease...

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UCB receives EU approval for paediatric anti-epileptic drug

22 September 2017 | By Dr Zara Kassam (European Pharmaceutical Review)

UCB has announced that the EC has approved the use of its anti-epileptic drug Vimpatas in the treatment of partial-onset seizures...

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Recommended

Committee for Medicinal Products for Human Use

European Commission revokes marketing authorisation for Novartis’ crizanlizumab

CHMP recommends Pluvicto® for treating advanced prostate cancer

Proposed biosimilar accepted for review by EMA

EMA grants marketing authorisation for Prevymis against cytomegalovirus

UCB receives EU approval for paediatric anti-epileptic drug

CHMP recommends Pluvicto^® for treating advanced prostate cancer