Brief: Gensight Biologics Announces Validation Of LUMEVOQ® Marketing Authorisation Application By EMA
Nov 3 (Reuters) - GENSIGHT BIOLOGICS SA SIGHT.PA :
* GENSIGHT BIOLOGICS REPORTS VALIDATION OF LUMEVOQ®
MARKETING
AUTHORISATION APPLICATION (MAA) BY EUROPEAN MEDICINES AGENCY
* IS ALSO WORKING TOWARDS SUBMITTING LUMEVOQ®'S BIOLOGICS
LICENSE
APPLICATION (BLA) TO U.S. FOOD AND DRUG ADMINISTRATION (FDA) IN
H2 2021.
Source text for Eikon: ID:nBw2xz0qla
Further company coverage: SIGHT.PA
(Gdansk Newsroom)
((gdansk.newsroom@thomsonreuters.com; +48 58 7785110;))
Recent news on Gensight Biologics SA
See all newsHealth Rounds: Blindness treatment based on Nobel-winning research shows promise
France's GenSight Biologics H1 net loss widens on higher R&D expenses
Brief: GenSight Biologics H1 Net Income EUR -10.3 Million
France's GenSight Biologics 2025 net loss narrows on reduced R&D spending
Brief: GenSight Biologics FY EPS EUR -0.08