Brief: EMA Says Application For Marketing Authorisation For The Advanced Therapy Medicinal Product Lumevoq Withdrawn
April 26 (Reuters) - Gensight Biologics SA SIGHT.PA :
* EMA SAYS APPLICATION FOR MARKETING AUTHORISATION FOR THE
ADVANCED THERAPY MEDICINAL PRODUCT LUMEVOQ WAS WITHDRAWN
* EMA: CHMP RECOMMENDED GRANTING EXTENSION OF INDICATION FOR
SPIKEVAX BIVALENT ORIGINAL/OMICRON BA.4-5 TO INCLUDE USE AS
BOOSTER IN CHILDREN AGED 6-11
* EMA - CHMP RECOMMENDED OPFOLDA FOR TREATMENT OF GLYCOGEN
STORAGE DISEASE TYPE II IN COMBINATION WITH CIPAGLUCOSIDASE ALFA
((Reuters.Briefs@thomsonreuters.com;))
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