Brief: Larimar Therapeutics Announces FDA Clearance To Initiate The 25 Mg Cohort Of A Phase 2 Dose Exploration Trial Of Cti-1601 In Friedreich’S Ataxia Patients
Sept 14 (Reuters) - Larimar Therapeutics Inc LRMR.O :
* LARIMAR THERAPEUTICS ANNOUNCES FDA CLEARANCE TO INITIATE
THE 25
MG COHORT OF A PHASE 2 DOSE EXPLORATION TRIAL OF CTI-1601 IN
FRIEDREICH’S ATAXIA PATIENTS
* LARIMAR THERAPEUTICS INC - INITIATION OF PHASE 2 TRIAL IS
EXPECTED IN Q4 2022, WITH TOP-LINE DATA EXPECTED IN 2H 2023
Source text for Eikon: ID:nGNX38Tdx
Further company coverage: LRMR.O
((Reuters.Briefs@thomsonreuters.com;))
Recent news on Larimar Therapeutics
See all newsU.S. STOCKS ON THE MOVE-Regenxbio, Repay, Natera, Fortune Brands
Larimar tumbles as safety concerns resurface in rare disease drug study update
U.S. STOCKS ON THE MOVE-Regenxbio, Repay, Natera, Fortune Brands
U.S. STOCKS ON THE MOVE-SpaceX, Charter, Gulfport Energy
Larimar tumbles as safety concerns resurface in rare disease drug study update