Sep 3European Commission Greenlights Keytruda and Padcev Combo as First-Line Treatment for Advanced Urothelial Carcinoma | iPharmaCenter
Sep 1European Commission Expands Approval for GSK's Arexvy, the First RSV Vaccine for Adults Aged 50-59 at Increased Risk | iPharmaCenter
Aug 27European Union Approves Ordspono for Treatment of Relapsed/Refractory Follicular Lymphoma and Diffuse Large B-cell Lymphoma | iPharmaCenter
Aug 24Leqembi (lecanemab) Approved in Great Britain for Early-Stage Alzheimer's Disease | iPharmaCenter
Aug 24The European Commission Grants Approval for Tepkinly for a New Indication in Treating Relapsed/Refractory Follicular Lymphoma in Adults | iPharmaCenter
Jul 2Committee for Medicinal Products for Human Use | CHMP Positive Opinion | June | Europe Drug Approvals | 2024 | iPharmaCenter
Jun 10European Commission Approves Roche's Alecensa as First Targeted Adjuvant Therapy for Early-Stage ALK-Positive Lung Cancer | 2024 | iPharmaCenter
May 31Biogen Gains European Commission Approval for QALSODY (tofersen), a Novel Therapy for a Rare Genetic Form of ALS | EMA Drug Approvals | 2024 | iPharmaCenter
Nov 17, 2023Medicines and Healthcare products Regulatory Agency | UK Drug approvals | News | iPharmaCenter
Oct 17, 2023EMA Drug Approvals | CHMP Positive Opinions in October 2023 | Europe drug approvals | iPharmaCenter
Sep 27, 2023Drug approvals in Europe| EMA drug approvals | 2023 |European Commission News| iPharmaCenter
May 16, 2023Medicines and Healthcare products Regulatory Agency | News | 2023 Approvals | iPharmaCenter
Jan 26, 2023Drug approvals in Europe| EMA drug approvals in 2022 |European Commission News| iPharmaCenter
Sep 19, 2022Opdualag was approved for unresectable/metastatic melanoma | LAG-3 inhibitors | Mode of action
Jan 12, 2021Biogen initiated Phase 4 trial to determine the efficacy of Spinraza in Zolgensma treated patients
Dec 28, 2020Kite’s CAR-Tcell therapy received approval in Europe for relapsed or refractory mantle cell lymphoma
Oct 9, 2020European Commission to purchase 200 million doses of Johnson and Johnson's COVID 19 vaccine
Oct 3, 2020HAS says Gilead's Veklury 'does not improve benefit' for COVID19 patients; EMA to review safety
Jul 3, 2020Gilead’s Veklury received conditional marketing authorization from the European Commission