Agios submits marketing authorisation application to European Medicines Agency for mitapivat for treatment of adults with pyruvate kinase deficiency

28 June 2021 - Agios Pharmaceuticals today announced that it has submitted a marketing authorisation application for mitapivat to the EMA ...

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BioMarin resubmits marketing authorisation application to European Medicines Agency for valoctocogene roxaparvovec to treat severe haemophilia A

28 June 2021 - Valoctocogene roxaparvovec MAA granted request for accelerated assessment. ...

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Chiasma announces submission of marketing authorisation application for Mycapssa to the European Medicines Agency

28 June 2021 - Submission supported by previously announced data from Phase 3 MPOWERED trial. ...

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Success rate for marketing authorisation applications from SMEs doubles between 2016 and 2020

28 June 2021 - EMA has published today a report highlighting the Agency’s support for micro, small and medium sized ...

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UCB receives positive CHMP opinion recommending approval of Bimzelx (bimekizumab) in the EU for the treatment of adults with moderate to severe plaque psoriasis

25 June 2021 - The positive CHMP opinion is supported by data from three Phase 3 trials where bimekizumab demonstrated superior ...

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Incyte and MorphoSys announce positive CHMP opinion for tafasitamab in combination with lenalidomide for the treatment of adults with relapsed or refractory diffuse large B-cell lymphoma

25 June 2021 - The positive opinion from the CHMP is based on data from the Phase 2 L-MIND study evaluating ...

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Astellas receives positive CHMP opinion for Evrenzo (roxadustat) for adult patients with symptomatic anaemia of chronic kidney disease

25 June 2021 - Astellas Pharma  today announced the CHMP of the EMA has adopted a positive opinion relating to the ...

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Forxiga recommended for approval in the EU by CHMP for the treatment of patients with chronic kidney disease

26 June 2021 - If approved, Forxiga has the potential to change the treatment paradigm for millions of people in ...

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Bristol Myers Squibb receives positive CHMP opinion for Opdivo (nivolumab) as adjuvant treatment for oesophageal or gastro-oesophageal junction cancer patients with residual pathologic disease following chemoradiotherapy

25 June 2021 - Recommendation based on positive results from the Phase 3 CheckMate -577 trial in which Opdivo doubled disease-free ...

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Libtayo (cemiplimab) approved by the European Commission as the first immunotherapy indicated for patients with advanced basal cell carcinoma

25 June 2021 - Approval based on data from the largest trial to date in patients with advanced basal cell carcinoma ...

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Libtayo (cemiplimab) approved by the European Commission for first-line treatment of patients with advanced non-small cell lung cancer with ≥50% PD-L1 expression

25 June 2021 - Approval based on a Phase 3 trial demonstrating Libtayo significantly improved overall survival compared to chemotherapy in ...

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BioMarin receives positive CHMP opinion in Europe for vosoritide for the treatment of children with achondroplasia from age 2 until growth plates close

25 June 2021 - Temporary Authorization for Use (ATU) granted in France to allow access and reimbursement of vosoritide to begin ...

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Bristol Myers Squibb receives positive CHMP opinion for anti-BCMA CAR T cell therapy Abecma (idecabtagene vicleucel) for relapsed and refractory multiple myeloma

25 June 2021 - Recommendation for approval based on results from pivotal KarMMa study. ...

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Samsung Bioepis and Biogen receive positive CHMP opinion for ranibizumab biosimilar, Byooviz

25 June 2021 - Samsung Bioepis and Biogen today announced that the EMA's CHMP has adopted a positive opinion for Byooviz, ...

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Highlights from 21-24 June CHMP meeting

25 June 2021 - EMA’s CHMP recommended eight medicines for approval at its June 2021 meeting. ...

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