Friday, July 10, 2026

pharma · Friedreich Ataxia · LRMR

Larimar Therapeutics

Larimar Therapeutics is a pharma organization headquartered in Bala Cynwyd, USA. It trades on NYSE under ticker LRMR. Primary therapeutic focus areas include Friedreich Ataxia. NovaPharmaNews links 3 clinical program(s),

Bala Cynwyd, USA HQ
2016 Founded
82 Employees
Public company Type
LRMR · NYSE Ticker
Company details
Status
Public
HQ
Bala Cynwyd, USA
Founded
2016
Employees
82
Programs
3
Drugs
2
Patents
5
Clinical program

Nomlabofusp, Placebo to Nomlabofusp

Phase 3 · small molecule · Friedreich’s ataxia is the most common inherited ataxia in humans and results from a deficiency of the mitochondrial protein, FXN. Friedreich’s ataxia is a rare, progressive, multisystem disease with an incidence that is estimated to be 1:29,000, and a carrier frequency of ~1:85.

Nomlabofusp, Placebo to Nomlabofusp for Friedreich’s ataxia is the most common inherited ataxia in humans and results from a deficiency of the mitochondrial protein, FXN. Friedreich’s ataxia is a rare, progressive, multisystem disease with an incidence that is estimated to be 1:29,000, and a carrier frequency of ~1:85. is a Phase 3 program (small_molecule) at Larimar Therapeutics with 1 ClinicalTrials.gov record(s).

← All Larimar Therapeutics projects Phase 3 small molecule active

Internal code CLIN-1601-301

Full intelligence profile for this program is being prepared.

At a glance

Sponsor
Larimar Therapeutics
Phase
Phase 3
Modality
small_molecule
Indication
Friedreich’s ataxia is the most common inherited ataxia in humans and results from a deficiency of the mitochondrial protein, FXN. Friedreich’s ataxia is a rare, progressive, multisystem disease with an incidence that is estimated to be 1:29,000, and a carrier frequency of ~1:85.
Status
active
Trials
1