CHMP adopts positive opinion recommending Hepcludex (bulevirtide) for full marketing authorization for the treatment of hepatitis delta virus

4 May 2023 - If granted by the European Commission, Hepcludex will become the only approved treatment for HDV in the ...

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Gene therapies are still hampered by substantial delays between approval and launch

3 May 2023 - Gene therapies hold promise for treating a wide range of diseases. Innovative companies such as bluebird bio ...

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Bristol Myers Squibb receives European Commission approval for CAR T cell therapy Breyanzi (lisocabtagene maraleucel) for relapsed or refractory large B-cell lymphoma after one prior therapy

3 May 2023 - Approval of Breyanzi based on the pivotal Phase 3 TRANSFORM trial, in which Breyanzi significantly improved ...

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US FDA accepts for priority review supplemental biologics license application and EMA validates application for Reblozyl (luspatercept-aamt) as first-line treatment of anaemia in adults with lower-risk myelodysplastic syndromes

1 May 2023 - Applications based on results from Phase 3 COMMANDS study in which first-in-class Reblozyl demonstrated a highly statistically ...

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CHMP issues positive opinion for futibatinib for the treatment of adults with cholangiocarcinoma

27 April 2023 - Taiho Pharmaceutical announced today that the EMA's CHMP has issued a positive opinion recommending the conditional ...

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UCB receives positive CHMP opinions for bimekizumab for the treatment of adults with psoriatic arthritis and axial spondyloarthritis in the European Union

27 April 2023 - Positive CHMP opinions are supported by data from four Phase 3 studies that evaluated bimekizumab in active ...

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Novartis Cosentyx gains positive CHMP opinion for hidradenitis suppurativa

26 April 2023 - Positive opinion paves way for first new treatment option in hidradenitis suppurativa in nearly a decade. ...

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CHMP recommends EU approval of Roche’s fixed-duration Columvi (glofitamab) for people with relapsed or refractory diffuse large B-cell lymphoma

26 April 2023 - The recommendation is based on results from the Phase I/II NP30179 study, where Columvi given as a ...

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Bristol Myers Squibb receives positive CHMP opinion recommending approval for Camzyos (mavacamten) for the treatment of symptomatic obstructive hypertrophic cardiomyopathy

26 April 2023 - Recommendation based on positive Phase 3 EXPLORER-HCM and VALOR-HCM trials demonstrating benefit in patients receiving Camzyos ...

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First vaccine to protect older adults from respiratory syncytial virus (RSV) infection

26 April 2023 - EMA has recommended a marketing authorisation in the European Union for Arexvy (recombinant, adjuvanted), the first vaccine ...

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Highlights from the 24-26 April 2023 CHMP meeting

26 April 2023 - The EMA’s CHMP recommended seven medicines for approval at its April 2023 meeting. ...

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Akebia receives European Commission approval for Vafseo (vadadustat) for the treatment of symptomatic anaemia associated with chronic kidney disease in adults on chronic maintenance dialysis

25 April 2023 -  -- Akebia Therapeutics today announced that the European Commission has granted marketing authorisation for Vafseo (vadadustat), ...

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Celltrion seeks approval for Xolair biosimilar in EU

25 April 2023 - Celltrion said it has completed a marketing authorization application for CT-P39, a biosimilar referencing Xolair (omalizumab) ...

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European Medicines Agency validates marketing authorisation application for Jemperli (dostarlimab) plus chemotherapy for the treatment of dMMR/MSI-H primary advanced or recurrent endometrial cancer

25 April 2023 - Regulatory submission based on pivotal data from Part 1 of the RUBY Phase 3 trial. ...

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EMA publishes agenda for 24-26 April 2023 CHMP meeting

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

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