Idorsia’s Jeraygo (aprocitentan) approved in Europe as first and only ERA for the treatment of resistant hypertension

 1 July 2024 - Jeraygo is a new oral antihypertensive therapy – the first in almost 40 years – that is ...

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Pierre Fabre Laboratories announce granting of European marketing authorisation for Obgemsa (vibegron) in overactive bladder

28 June 2024 - The European Commission has authorised the marketing of Obgemsa (vibegron) by Pierre Fabre Laboratories for the symptomatic ...

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CHMP recommends EU approval of Roche’s PiaSky for people with PNH, a rare, life-threatening blood condition

28 June 2024 - The recommendation is based on the COMMODORE 2 study results, where SC PiaSky given every month demonstrated ...

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Sipavibart EMA regulatory submission accepted under accelerated assessment for COVID-19 prevention

1 July 2024 - Submission based on positive SUPERNOVA Phase 3 trial data which demonstrated a statistically significant reduction in ...

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Lynparza and Imfinzi combination recommended for approval in the EU by CHMP for patients with mismatch repair proficient advanced or recurrent endometrial cancer

1 July 2024 - Recommendation based on DUO-E Phase 3 results, which showed both regimens demonstrated statistically significant and clinically ...

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Roche’s Vabysmo gets CHMP recommendation for third indication retinal vein occlusion

28 June 2024 - Positive recommendation is based on two Phase 3 studies. In addition to robust retinal drying with Vabysmo, ...

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Highlights from the 24-27 June 2024 CHMP meeting

28 June 2024 - The EMA’s CHMP recommended ten medicines for approval at its June 2024 meeting. ...

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AbbVie receives positive CHMP opinion for epcoritamab (Tepkinly) for the treatment of adults with relapsed/refractory follicular lymphoma

28 June 2024 - Positive CHMP opinion based on results from the Phase 1/2 EPCORE NHL-1 study. ...

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Tofidence (tocilizumab), a biosimilar referencing RoActemra, approved in the European Union

24 June 2024 - Tofidence complements existing portfolio of immunology biosimilars commercialised by Biogen ...

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Roche’s Ocrevus subcutaneous administration approved by European Commission, as first and only twice-a-year injection for relapsing and primary progressive multiple sclerosis

25 June 2024 - Roche is working closely with national health systems in Europe to ensure people with multiple sclerosis ...

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EMA publishes agenda for June 24-27 2024 CHMP meeting

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

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Jemperli (dostarlimab) plus chemotherapy application accepted for review by the EMA to expand use to all patients with primary advanced or recurrent endometrial cancer

24 June 2024 - Regulatory submission supported by statistically significant and clinically meaningful progression-free and overall survival data from Part 1 ...

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Takeda receives approval from European Commission for Fruzaqla in previously treated metastatic colorectal cancer

21 June 2024 - Approval based on results from positive, global, Phase 3 FRESCO-2 trial. ...

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European Medicines Agency validates Bristol Myers Squibb’s application for subcutaneous nivolumab

21 June 2024 - Validation is based on results from CheckMate -67T, the first Phase 3 trial of the subcutaneous formulation ...

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Truqap plus Faslodex approved in the EU for patients with advanced oestrogen receptor positive breast cancer

20 June 2024 - Approval based on CAPItello-291 results which showed this combination reduced the risk of disease progression or ...

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