Jan 3 (Reuters) - Gensight Biologics SA SIGHT.PA :
* A SCIENTIFIC ADVICE CONFIRMS UK MHRA COULD ACCEPT A
MARKETING
AUTHORISATION APPLICATION FOR LUMEVOQ® WITH THE MOST RECENT
CLINICAL DATA FROM EXISTING TRIALS (NOT NECESSARILY INCLUDING
RECOVER DATA)
* PLANS TO FILE AN APPLICATION FOR A MARKETING AUTHORISATION
IN
THE UK IN H2 2024, AIMING FOR A POSSIBLE DECISION BY H2 2025
* DECISION TO MIX TWO SUCCESSFUL DRUG SUBSTANCE BATCHES INTO
ONE
SINGLE DRUG PRODUCT BATCH; PRODUCT NOW EXPECTED TO BE FULLY
RELEASED IN Q3 2024 (VERSUS EARLY Q2 2024 PREVIOUSLY)
* EXTENDED CASH RUNWAY TO MID-FEBRUARY 2024
* ONGOING DISCUSSIONS TO BRIDGE AAC RESUMPTION IN FRANCE IN
Q3
2024; ESTIMATED NEED AMOUNTING TO €14 MILLION
Source text: http://tinyurl.com/yu5br8kh
Further company coverage: SIGHT.PA
(Gdansk Newsroom)
((gdansk.newsroom@thomsonreuters.com; +48 58 7696600;))