Company intelligence / Profile preview

IntraBio

Ownership: Private
Development stage: Phase 3

Overview

IntraBio has achieved FDA approval for AQNEURSA (modified amino acid) to treat neurological manifestations of Niemann-Pick type C. Its lead program IB1001 completed a pivotal Phase III trial in mid-June 2023. The company’s pipeline includes additional assets targeting rare and common neurodegenerative diseases. Clinical results have been published in leading medical journals; the company has moved its HQ from Oxford, UK to Austin, Texas.

Therapeutic areas: Rare DiseasesNeurology
Modalities: Small molecules (notably modified amino acids such as N-Acetyl-L-Leucine)
Industry: Biotech

Drug pipeline

7 assets

levacetylleucine

Approved

6 more assets in the full pipeline.

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Partnerships

None specifically named; collaborations with academic institutions are noted.

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