Sept 23 (Reuters) - Nicox SA NCOX.PA :
* ANNOUNCES RESULTS FROM THE NCX 4251 PHASE 2B MISSISSIPPI
BLEPHARITIS TRIAL
* TRIAL DID NOT MEET PRIMARY OR SECONDARY EFFICACY ENDPOINTS
* PLEASED TO SEE THAT THERE IS A SIGNAL OF EFFICACY IN
COMPOSITE
SCORE OF SIGNS AND SYMPTOMS OF BLEPHARITIS
* TRIAL DID NOT MEET PRIMARY OR SECONDARY EFFICACY ENDPOINTS
* NEXT STEPS AND TIMELINES IN DEVELOPMENT OF NCX 4251 WILL
BE
ANNOUNCED FOLLOWING A MEETING WITH U.S. FOOD AND DRUG
ADMINISTRATION, EXPECTED TO TAKE PLACE AT BEGINNING OF 2022
* A SIGNAL OF NCX 4251'S POTENTIAL EFFICACY WAS SEEN IN
TRIAL WITH
NCX 4251 0.1% SHOWING A NUMERICAL IMPROVEMENT OVER PLACEBO IN
PRIMARY OUTCOME MEASURE
* BLEPHARITIS IS A COMMON EYE CONDITION CHARACTERIZED BY
EYELID
INFLAMMATION
* NCX 4251 ALSO SHOWED A STATISTICALLY SIGNIFICANT
DIFFERENCE
AGAINST PLACEBO IN EXPLORATORY ENDPOINT
* NCX 4251 WAS FOUND TO BE SAFE AND WELL-TOLERATED OVER 14
DAYS'
TREATMENT
* ALL OF ADVERSE EVENTS FOR NCX 4251 TREATMENT ARM WERE MILD
* THERE WERE NO DISCONTINUATIONS IN STUDY DUE TO AN ADVERSE
EVENT
Source text for Eikon: ID:nGNX1YC0Z2
Further company coverage: NCOX.PA
(Gdansk Newsroom)
((gdansk.newsroom@thomsonreuters.com; +48 58 769 66 00;))