Zepzelca (lurbinectedin) in combination with atezolizumab approved by the European Commission as first-line maintenance therapy for extensive-stage small cell lung cancer

1 June 2026 - Immedica today announces that the European Commission has granted marketing authorisation for Zepzelca (lurbinectedin), in combination with ...

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Samsung Bioepis launches Opuviz (aflibercept) 40 mg/mL vial across Europe, to treat ophthalmic conditions

29 May 2026 - Samsung Bioepis today announced the launch of Opuviz 40 mg/mL solution for injection in a vial, ...

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AbbVie announces European Commission authorisation of expanded label for Venclyxto (venetoclax) to include additional combinations in previously untreated chronic lymphocytic leukaemia

29 May 2026 - AbbVie today announced that the European Commission (EC) has authorised an expanded label for Vencylxto (venetoclax) to ...

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Avanzanite Bioscience’s partner Agios announces Pyrukynd (mitapivat) approval in the European Union for adults with thalassaemia

22 May 2026 - Avanzanite Bioscience today reported that its partner, Agios Pharmaceuticals announced that the European Commission has granted marketing ...

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First medicine to treat rare uncontrolled growth of body tissues

22 May 2026 - Vijoice addresses an unmet medical need for patients with severe or life-threatening PIK3CA-related overgrowth spectrum disorders. ...

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New medicine for two types of pulmonary fibrosis

22 May 2026 - Jascayd slowed loss of lung function in patients with idiopathic or progressive pulmonary fibrosis. ...

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First oral GLP-1 treatment for weight management

22 May 2026 - EMA has recommended an extension to the marketing authorisation for Wegovy (semaglutide) in the EU to add ...

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Henlius’ serplulimab receives positive CHMP opinion for the treatment of sqNSCLC

23 May 2026 - Henlius Biotech announced that serplulimab (Hetronifly), the company’s self-developed anti-PD-1 mAb, has received a positive opinion from ...

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Otarmeni (lunsotogene parvec) receives EMA filing acceptance for genetic hearing loss

22 May 2026 - Regeneron Pharmaceuticals today announced the EMA has accepted for review under accelerated assessment the marketing authorisation application ...

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Camizestrant in combination with a CDK4/6 inhibitor recommended for approval in the EU by CHMP for 1st-line advanced ER-positive breast cancer

22 May 2026 - Recommendation based on SERENA-6 Phase 3 trial results which showed combination reduced the risk of disease progression ...

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AbbVie announces positive CHMP opinion for Maviret (glecaprevir/pibrentasvir) for the treatment of acute hepatitis C infection

22 May 2026 - The positive opinion is supported by data from the Phase 3 M20-350 study evaluating the safety and ...

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Enhertu recommended for approval in the EU by CHMP for patients with previously treated HER2-positive metastatic solid tumours

22 May 2026 - Based on three Phase 2 trials of AstraZeneca and Daiichi Sankyo’s Enhertu which showed clinically meaningful responses ...

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The EMA accepts Teva’s marketing authorisation application for olanzapine long-acting injectable for the treatment of schizophrenia in adults

21 May 2026 - Teva Pharmaceuticals and Medincell today announced that the EMA has accepted the marketing authorisation application for olanzapine ...

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Allergan Aesthetics receives positive CHMP opinion for Boey (trenibotulinumtoxinE) for the temporary improvement of moderate to severe glabellar lines in adults

21 May 2026 - Positive opinion is supported by data from two pivotal Phase 3 trials, which demonstrated rapid results as ...

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EMA publishes agenda for 18-21 May 2026 CHMP meeting

18 May 2026 - The EMA has published a draft agenda for this week's CHMP meeting. ...

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