April 26 (Reuters) - Gensight Biologics SA:
* EMA SAYS APPLICATION FOR MARKETING AUTHORISATION FOR THE ADVANCED THERAPY MEDICINAL PRODUCT LUMEVOQ WAS WITHDRAWN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