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Rhythm Pharmaceuticals Receives Positive CHMP Opinion for ▼¹ IMCIVREE® (setmelanotide) for the Treatment of Obesity and Control of Hunger in Patients

BOSTON, July 22, 2022 (GLOBE NEWSWIRE) -- Rhythm Pharmaceuticals, Inc. (Nasdaq: RYTM), a commercial-stage biopharmaceutical company focused on transforming the lives of patients and their families living with hyperphagia and severe obesity caused by rare melanocortin-4 receptor (MC4R) pathway diseases, today announc...
United States United Kingdom Great Britain Philip Beales David Meeker University College London

F. Hoffmann-La Roche Ltd: CHMP recommends EU approval of Roche's Vabysmo, the first bispecific antibody for the eye, for two leading causes of vision loss

Vabysmo (faricimab) simultaneously targets and inhibits two disease pathways that drive neovascular or "wet" age-related macular degeneration (nAMD) and diabetic macular edema (DME)The CHMP recommendation
United States United Kingdom Levi Garraway Birgit Masjost Loren Kalm Sabine Borngr

DGAP-News: EMA Committee for Medicinal Products for Human Use (CHMP) Recommends Use of the Moderna COVID-19 Booster in Adolescents (12-17 Years) in the European Union

DGAP-News: Moderna, Inc. / Key word(s): Miscellaneous EMA Committee for Medicinal Products for Human Use (CHMP) Recommends Use of the Moderna COVID-19 Booster in Adolescents (12-17 Years) in the European Union 22.07.2022 / 14:05 The issuer is solely responsible for the content of this announceme...
United Kingdom Lavina Talukdar Luke Mircea Willats European Commission Distribution Services Exchange Commission

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Alnylam Pharmaceuticals, Inc.: Alnylam Receives Positive CHMP Opinion for Vutrisiran for the Treatment of Hereditary Transthyretin-mediated (hATTR) Amyloidosis in Adult Patients with Stage 1 or Stage 2 Polyneuropathy

Positive Opinion Based on HELIOS-A Phase 3 Study European Commission Decision Expected in September 2022 - Alnylam Pharmaceuticals, Inc. (Nasdaq: ALNY), the leading RNAi therapeutics company, today
United Kingdom United States Emily Bunting Christine Regan Lindenboom Josh Brodsky Kasha Witkos

Karyopharm and Menarini Group Receive Full Marketing Authorisation from the European Commission for NEXPOVIO (selinexor) for the Treatment of Patients with Multiple Myeloma After at Least One Prior Therapy

- Based on Results from Phase 3 BOSTON Study, Marketing Authorisation Expands Multiple Myeloma Indication - - Approval Follows Positive Opinion by European Committee for Medicinal Products for Human Use (CHMP) in May 2022 - NEWTON, Mass.andFLORENCE, Italy, July 21, 2022 /PRNewswire/ -- Karyopharm Therapeutics Inc. (Nasdaq:KPTI), a commercial-stage pharmaceutical company pioneering novel cancer therapies, and the Menarini Group ("Menarini"), a privately-held, leading international pharm...
United States United Kingdom South Korea Northern Ireland Richard Paulson Elcin Barker Ergun

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