July 17 (Reuters) - Coya Therapeutics Inc COYA.O :
* COYA THERAPEUTICS REPORTS ADDITIONAL PROOF-OF-CONCEPT
CLINICAL
BIOMARKER DATA IN PATIENTS WITH ALZHEIMER’S DISEASE
* COYA THERAPEUTICS INC - TREATMENT WITH LD IL-2
ADMINISTERED
SUBCUTANEOUSLY APPEARED TO BE SAFE AND WELL TOLERATED IN
PATIENTS WITH AD
* COYA THERAPEUTICS - ONGOING PHASE 2, DOUBLE BLIND, PLACEBO
CONTROLLED TRIAL IS ALMOST FULLY ENROLLED, SHOULD REPORT TOP
LINE RESULTS IN JULY, 2024
* COYA THERAPEUTICS INC - OVERALL, ADMINISTRATION OF LD-IL-2
APPEARED TO BE SAFE AND WELL TOLERATED
* COYA THERAPEUTICS INC - MOST COMMON ADVERSE EVENTS OF
LD-IL-2
WERE MILD INJECTION-SITE REACTIONS AND MILD LEUKOPENIA
* COYA THERAPEUTICS INC - NO SERIOUS ADVERSE EVENTS WERE
REPORTED,
AND NO PATIENT DISCONTINUED STUDY
Source text for Eikon: ID:nBw4xsnnVa
Further company coverage: COYA.O
((Reuters.Briefs@thomsonreuters.com;))