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Moderna, Inc.: EMA Committee For Medicinal Products For Human Use Adopts Positive Opinion Recommending Authorization Of Moderna's Omicron BA.4-BA.5 Targeting Bivalent Covid-19 Vaccine In The European Union

Positive recommendation follows the recent approval of Spikevax bivalent Original/Omicron BA.1 (mRNA-1273.214), a bivalent booster vaccine targeting the Omicron BA.1 subvariant, in SeptemberCAMBRIDGE,
United States United Kingdom South Korea Lavina Talukdar Luke Mircea Willats European Commission

Investegate |BioNTech SE Announcements | BioNTech SE: Pfizer and BioNTech Receive Positive CHMP Opinion for COMIRNATY® in Children 6 Months to less than 5 Years in the European Union

Investegate announcements from BioNTech SE, Pfizer and BioNTech Receive Positive CHMP Opinion for COMIRNATY® in Children 6 Months to less than 5 Years in the European Union
United States United Kingdom Sylke Maas Fosun Pharma European Commission Drug Administration

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COMP adopts positive opinion on Orphan Disease Designation for Mycapssa for the treatment of Acromegaly

18.10.2022 - COMP adopts positive opinion on Orphan Disease Designation for Mycapssa for the treatment of Acromegaly DUBLIN, Ireland, and Boston MA, October 18, 2022 Amryt (Nasdaq: AMYT), a global, commercial-stage biopharmaceutical company dedicated to ... Seite 1
United States Joe Wiley Myalept Myalepta Juxtapid Lojuxta Amryt Pharma Committee For Orphan Medicinal Products

Investegate |NOVARTIS AG CHF0.50(REGD) Announcements | NOVARTIS AG CHF0.50(REGD): Novartis receives positive CHMP opinion for Pluvicto® for patients with progressive, PSMA-positive metastatic castration-resistant prostate cancer

Investegate announcements from NOVARTIS AG CHF0.50(REGD), Novartis receives positive CHMP opinion for Pluvicto® for patients with progressive, PSMA-positive metastatic castration-resistant prostate cancer
France General United States Northern Ireland United Kingdom Isabella Zinck Karim Fizazi

Atara Biotherapeutics, Inc.: CHMP Recommends Approval of Atara Biotherapeutics' Ebvallo (tabelecleucel) for the Treatment of Epstein-Barr Virus-Positive Post-Transplant Lymphoproliferative Disease

EbvalloTM on Track to be the First Ever Allogeneic T-Cell Therapy Approved Positive Opinion Based on Pivotal Phase 3 ALLELE Study Demonstrating a Favorable Risk-Benefit Profile European Commission
United States South San Francisco United Kingdom Pierre Fabre Eric Hyllengren Alex Chapman

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