Merck receives positive EU CHMP opinion for Keytruda (pembrolizumab) plus chemotherapy as first-line treatment for adult patients with unresectable non-epithelioid malignant pleural mesothelioma

15 November 2024 - Opinion granted based on positive overall survival results from the IND.227/KEYNOTE-483 trial. ...

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Tagrisso recommended for approval in the EU by CHMP for patients with unresectable EGFR mutated lung cancer

18 November 2024 - Recommendation based on LAURA Phase 3 trial results which showed Tagrisso extended median progression-free survival to ...

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AbbVie receives European Commission approval of Elahere (mirvetuximab soravtansine) for the treatment of platinum resistant ovarian cancer

18 November 2024 - VENTANA FOLR RxDx assay, the companion diagnostic to identify ovarian cancer patients eligible for Elahere, also ...

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Azurity Pharmaceuticals announces FDA approval of Danziten (nilotinib) tablets, the first and only nilotinib with no mealtime restrictions

14 November 2024 - Azurity Pharmaceuticals announced today that the US FDA has approved Danziten, the first and only nilotinib with ...

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AlveoGene receives rare paediatric disease designation from FDA for AVG-002, its novel, inhaled gene therapy for lethal neonatal surfactant protein B deficiency

15 November 2024 -  AlveoGene announces that it has been granted a rare paediatric disease designation by the US FDA ...

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Bristol Myers Squibb receives positive CHMP opinion for repotrectinib for the treatment of advanced ROS1 positive non-small cell lung cancer and advanced NTRK positive solid tumours

15 November 2024 - Recommendation based on data from registrational TRIDENT-1 and CARE trials, which demonstrated robust responses and durable activity ...

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Bristol Myers Squibb receives positive CHMP opinion for Opdivo (nivolumab) plus Yervoy (ipilimumab) for the first-line treatment of adult patients with microsatellite instability–high or mismatch repair deficient metastatic colorectal cancer

15 October 2024 - Opinion based on results from the Phase 3 CheckMate-8HW trial, in which the dual immunotherapy combination ...

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FDA approves revumenib for relapsed or refractory acute leukaemia with a KMT2A translocation

15 November 2024 - Today, the FDA approved revumenib (Revuforj, Syndax Pharmaceuticals), a menin inhibitor, for relapsed or refractory acute ...

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Highlights from the 11-14 November 2024 CHMP meeting

15 November 2024 - The EMA’s CHMP has recommended eight medicines for approval at its November 2024 meeting. ...

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Dupixent (dupilumab) sBLA accepted for FDA review for the treatment of chronic spontaneous urticaria

15 November 2024 - Resubmission includes new pivotal data which confirm Dupixent significantly reduced itch and hive activity. ...

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Sandoz receives European Commission approval for Afqlir (aflibercept), further strengthening leading biosimilar portfolio

15 November 2024 - Afqlir (aflibercept) approved to treat various retinal diseases, including neovascular age-related macular degeneration. ...

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Leqembi recommended for treatment of early Alzheimer’s disease

14 November 2024 - After re-examining its initial opinion, EMA’s CHMP has recommended granting a marketing authorisation to Leqembi (lecanemab) ...

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Knight Therapeutics announces Health Canada approval for Jornay PM to treat attention deficit hyperactivity disorder

14 November 2024 - Knight Therapeutics announced today that Health Canada has approved Jornay PM, an extended-release formulation of methylphenidate, a ...

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Leo Pharma’s Anzupgo (delgocitinib) cream achieves marketing approval in Switzerland

14 November 2024 - In addition to the results of the DELTA 1,2 and 3 trials, the marketing approval is supported ...

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EMA publishes agenda for 11-14 November 2024 CHMP meeting

11 November 2024 - - The EMA has published a draft agenda for this week's CHMP meeting. ...

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