Wednesday, July 8, 2026

pharma · Friedreich Ataxia · LRMR

Larimar Therapeutics

Larimar Therapeutics trial registry — 6 ClinicalTrials.gov studies with program phase, status, and indication context.

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
Intelligence · Clinical Trials

Larimar Therapeutics clinical trials

Registry index of 6 ClinicalTrials.gov studies linked to Larimar Therapeutics programs — each row shows trial ID, program name, phase, status, and indication.

Larimar Therapeutics trial registry — 6 ClinicalTrials.gov studies with program phase, status, and indication context.

Recent trial activity

3 updates

Latest clinical program signals indexed for Larimar Therapeutics.

  1. Nomlabofusp, Placebo to Nomlabofusp — Phase 3

    Clinical update
  2. CTI-1601 — Phase 2

    Clinical update
  3. Nomlabofusp — Phase 1

    Clinical update

Trial registry

6 studies
  1. 2025-521628-31-00

    Nomlabofusp, Placebo to Nomlabofusp

    Phase 3 active 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.

    CTIS ↗