Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Oruvestat (VTG-001) is an orally bioavailable, potent, and selective small molecule inhibitor of Vascular Adhesion Protein-1 (VAP-1), also known as Amine Oxidase Copper Containing 3 (AOC3). VAP-1 is a dual-function protein acting as both an adhesion molecule and a semicarbazide-sensitive amine oxidase (SSAO) enzyme that facilitates leukocyte recruitment to inflamed tissues. By inhibiting the enzymatic activity of VAP-1, oruvestat reduces the inflammatory response and subsequent fibrosis, positioning it as a therapeutic candidate for inflammatory and fibrotic conditions. Originally developed by Pharmaxis as PXS-4728A and previously licensed to Boehringer Ingelheim as BI 1467335, the asset was acquired by Vantage Biosciences for development in non-proliferative diabetic retinopathy (NPDR), metabolic dysfunction-associated steatohepatitis (MASH), and primary sclerosing cholangitis (PSC).
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on oruvestat.