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ITF Therapeutics

Concord, Massachusetts, United Statesitftherapeutics.com ↗
Ownership
Private
Development stage
Commercial
01

Overview

ITF Therapeutics launched in January 2024 as the U.S. rare disease affiliate of Italfarmaco. Its lead product, DUVYZAT™ (givinostat), a histone deacetylase inhibitor for Duchenne muscular dystrophy in patients aged six and older regardless of genetic mutation, received FDA approval on March 21, 2024 and is now commercially available in the U.S.[2][5] The company has rapidly built out its team and infrastructure to support commercialization and patient access.

Therapeutic areas
Rare Diseases
Modalities
Small molecules (notably, histone deacetylase inhibitors)[5]
Industry
Biotech
02

Drug pipeline

1 asset

givinostat

Commercial
Indications
Duchenne muscular dystrophy
03

Partnerships

Collaborates closely with patient advocacy groups in rare diseases; no major pharma partnerships disclosed beyond relationship with parent Italfarmaco[1][6].

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