Feb 12 (Reuters) - Larimar Therapeutics Inc LRMR.O :
* LARIMAR THERAPEUTICS REPORTS POSITIVE TOP-LINE DATA FROM
PHASE 2
DOSE EXPLORATION STUDY FROM 25 MG AND 50 MG COHORTS OF
NOMLABOFUSP IN PATIENTS WITH FRIEDREICH’S ATAXIA
* LARIMAR THERAPEUTICS INC: DOSE DEPENDENT INCREASES IN
FRATAXIN
LEVELS WERE OBSERVED IN SKIN AND BUCCAL CELLS
* LARIMAR THERAPEUTICS INC: INITIATED DISCUSSIONS WITH FDA
ON USE
OF TISSUE FRATAXIN LEVELS AS A NOVEL SURROGATE ENDPOINT TO
SUPPORT A POTENTIAL BLA
* LARIMAR THERAPEUTICS INC: NOMLABOFUSP WAS GENERALLY WELL
TOLERATED
* LARIMAR THERAPEUTICS INC: BIOLOGICS LICENSE APPLICATION
SUBMISSION FOR ACCELERATED APPROVAL TARGETED FOR 2H 2025
* LARIMAR THERAPEUTICS INC: EXPECT TO PROVIDE INTERIM DATA
FROM
OLE STUDY IN Q4 OF 2024
Source text for Eikon: ID:nGNX24gSlc
Further company coverage: LRMR.O
((Reuters.Briefs@thomsonreuters.com;))