July 8 (Reuters) - Longeveron Inc LGVN.O:
LONGEVERON® ANNOUNCES U.S. FDA APPROVAL OF IND APPLICATION FOR A PHASE 2 PIVOTAL REGISTRATION STUDY EVALUATING LAROMESTROCEL AS A TREATMENT OF PEDIATRIC DILATED CARDIOMYOPATHY (DCM)
LONGEVERON INC - PHASE 2 TRIAL INITIATION EXPECTED IN FIRST HALF OF 2026
Source text: ID:nGNXJ3bvK
Further company coverage: LGVN.O
((((Reuters.Briefs@thomsonreuters.com));))