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Larimar Therapeutics

Bala Cynwyd, Pennsylvania, United Stateslarimartx.com ↗
Ownership
Public · LRMR
Employees
~65
Development stage
Phase 2
01

Overview

Larimar’s lead candidate nomlabofusp (formerly CTI–1601) has shown dose-dependent increases in frataxin levels and was generally well tolerated with no serious adverse events in Phase 2 studies. The FDA has selected the program for its START pilot to accelerate development. An open-label extension study continues enrolling, and a global Phase 3 trial will begin mid–2025. The company aims to submit a BLA by year-end 2025 seeking accelerated approval using skin FXN concentration as a surrogate endpoint.

Therapeutic areas
Neurology
Modalities
Protein replacement therapy (fusion proteins)Cell penetrating peptide technology
Industry
Biotech
02

Drug pipeline

5 assets

beloranib

3

4 more assets in the full pipeline.

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03

Partnerships

Friedreich’s Ataxia Research Alliance / TRACK–FA Neuroimaging Consortium academic/industry collaboration
04

Financials

Market cap
$402M
Total revenue
$0
Enterprise value
$250.7M

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