Highlights from the 11-14 September 2023 CHMP meeting

15 September 2023 - The EMA’s CHMP recommended nine medicines for approval at its September 2023 meeting. ...

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argenx announces positive CHMP opinion for subcutaneous efgartigimod for generalised myasthenia gravis

15 September 2023 - Positive opinion based on Phase 3 ADAPT-SC study demonstrating non-inferior total IgG reduction at day 29 with ...

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Quizartinib recommended for approval in EU by CHMP for patients with newly diagnosed FLT3-ITD positive AML

15 September 2023 - Positive opinion based on QuANTUM-First results demonstrating quizartinib combined with standard chemotherapy improved overall survival. ...

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EMA recommends non-renewal of authorisation of Duchenne muscular dystrophy medicine Translarna

15 September 2023 - EMA’s human medicines committee (CHMP) has recommended not renewing the marketing authorisation for Translarna (ataluren), a ...

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Merck receives positive EU CHMP opinion for Keytruda (pembrolizumab) as adjuvant treatment for adults with non-small cell lung cancer at high risk of recurrence following complete resection and platinum-based chemotherapy

15 September 2023 - Opinion granted based on positive disease-free survival results from the Phase 3 KEYNOTE-091 trial. ...

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Enhertu recommended for approval in the EU by CHMP for patients with HER2 mutant advanced non-small cell lung cancer

15 September 2023 - Recommendation based on DESTINY-Lung02 trial results which showed AstraZeneca and Daiichi Sankyo’s Enhertu achieved strong and durable ...

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UCB receives CHMP positive opinion of zilucoplan for the treatment of adults with generalized myasthenia gravis in Europe

15 September 2023 - The CHMP positive opinion is based on the pivotal Phase 3 RAISE study in generalised myasthenia gravis ...

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Spikevax: EMA recommends approval of adapted COVID-19 vaccine targeting Omicron XBB.1.5

14 September 2023 - EMA’s human medicines committee (CHMP) has recommended authorising an adapted Spikevax vaccine targeting the Omicron XBB.1.5 ...

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EMA publishes agenda for 11-14 September 2023 CHMP meeting

11 September 2023 - The EMA has published a draft agenda for this week's CHMP meeting. ...

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European Commission expands Merck’s Ervebo [Ebola Zaire vaccine, live] indication to include children 1 year of age and older

7 September 2023 - Milestone signifies on-going effort to help prepare for outbreaks of Zaire ebolavirus. ...

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Janssen submits marketing authorisation application to the EMA seeking approval of erdafitinib for the treatment of patients with locally advanced or metastatic urothelial cancer with susceptible FGFR alterations

8 September 2023 - The submission is based on results from the Phase 3 THOR study, which were featured in ...

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Italfarmaco Group receives EMA validation of marketing authorisation application for givinostat in Duchenne muscular dystrophy

5 September 2023 - Italfarmaco Group announced today that its marketing authorisation application for givinostat as a potential treatment for ...

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SK Bioscience withdraws conditional marketing authorisation for COVID-19 vaccine in EU

4 September 2023 - SK Bioscience said it has voluntarily withdrawn its application for a conditional marketing authorisation license to ...

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InflaRx’s marketing authorisation application for vilobelimab for treatment of critically ill COVID-19 patients under review by European Medicines Agency

30 August 2023 - Regulatory submission based on pivotal data from PANAMO Phase III trial. ...

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EMA recommends approval of adapted COVID-19 vaccine targeting Omicron XBB.1.5

30 August 2023 - The EMA’s CHMP has recommended authorising an adapted Comirnaty vaccine targeting the Omicron XBB.1.5 subvariant. ...

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