EMA starts evaluating use of Olumiant in hospitalised COVID-19 patients requiring supplemental oxygen

29 April 2021 - EMA has started evaluating an application to extend the use of Olumiant (baricitinib) to include treatment ...

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Vertex announces European Commission approval for Kaftrio (ivacaftor/tezacaftor/elexacaftor) in combination with ivacaftor to treat cystic fibrosis patients 12 years and older with at least one F508del mutation in the CFTR gene

28 April 2021 - New indication includes people ages 12 years and older who have one copy of the F508del mutation ...

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Y-mAbs submits omburtamab marketing authorisation application to the EMA

27 April 2021 - Y-mAbs Therapeutics today announced that the Company has submitted its marketing authorisation application to the European Medicines ...

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EMA grants accelerated assessment procedure for Nefecon for the treatment of IgA nephropathy

23 April 2021 - Calliditas Therapeutics today announced that its lead product candidate Nefecon, a novel oral formulation targeting down regulation ...

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Glenmark’s Ryaltris nasal spray now approved in Europe for the first-line treatment of allergic rhinitis in patients over 12 years of age

26 April 2021 - This marks Glenmark’s first innovative product approval in the European Union. ...

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Karyopharm announces European Medicines Agency's validation of its type II variation marketing authorisation application for Nexpovio (selinexor) in combination with Velcade (bortezomib) and dexamethasone for the treatment of adult patients with multiple myeloma

26 April 2021 - EMA regulatory decision expected in the fourth quarter of 2021. ...

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The European Union sues AstraZeneca over missing vaccine doses

26 April 2021 - The European Union has sued AstraZeneca over what the bloc has described as delays in shipping ...

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EMA and ECDC join forces for enhanced post-marketing monitoring of COVID-19 vaccines in Europe

26 April 2021 - The EMA and the European Centre for Disease Prevention and Control today kicked off a new ...

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Vertex and CRISPR Therapeutics announce Priority Medicines (PRIME) designation granted by the European Medicines Agency to CTX001 for transfusion-dependent beta thalassaemia

26 April 2021 - Vertex Pharmaceuticals and CRISPR Therapeutics today announced the EMA has granted Priority Medicines (PRIME) designation to ...

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Selumetinib recommended for approval in the EU by CHMP as the first medicine for paediatric patients with neurofibromatosis type 1 and plexiform neurofibromas

26 April 2021 - Recommendation based on the SPRINT Phase 2 trial, which showed selumetinib reduced tumour volume in children. ...

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Tagrisso recommended for approval in the EU by CHMP for the adjuvant treatment of patients with early-stage EGFR-mutated lung cancer

26 April 2021 - Opinion based on unprecedented results from the ADAURA Phase 3 trial where Tagrisso reduced the risk of ...

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European Commission approves GSK’s Jemperli (dostarlimab), the first anti-PD-1 therapy approved for recurrent or advanced endometrial cancer

23 April 2021 - The approval makes dostarlimab the first anti-PD-1 therapy available for endometrial cancer in Europe. ...

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LEO Pharma receives positive CHMP opinion of Adtralza (tralokinumab) for the treatment of adults with moderate-to-severe atopic dermatitis

23 April 2021 - The CHMP opinion is primarily supported by data from ECZTRA 1, 2, and 3 trials included in ...

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Bristol Myers Squibb receives positive CHMP opinion recommending approval for Opdivo (nivolumab) plus Yervoy (ipilimumab) as first-line treatment for unresectable malignant pleural mesothelioma

23 April 2021 - Recommendation based on positive results from the Phase 3 CheckMate-743 trial, in which Opdivo plus Yervoy demonstrated ...

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Bristol Myers Squibb receives positive CHMP opinion for Onureg (azacitidine tablets; CC-486) as frontline oral maintenance therapy for adults with acute myeloid leukaemia in first remission

23 April 2021 - In the pivotal Quazar AML-001 study, Onureg demonstrated significant overall survival and showed a relapse-free survival benefit ...

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