Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
VTB-10 is a first-in-class drug candidate developed by Vasthera using its proprietary Redoxizyme platform for the treatment of pulmonary arterial hypertension (PAH), a rare and progressive disease characterized by elevated blood pressure in the lung arteries. VTB-10 is a small molecule enzyme ("Chemzyme") designed to precisely replicate peroxiredoxin (PRX) function, an enzyme found deficient in PAH lesions. Mechanistically, VTB-10 works by inhibiting intimal hyperplasia through targeting **PDGFR signaling** in pulmonary arterial smooth muscle cells and promoting re-endothelialization by restoring **VEGFR2 signaling** in pulmonary arterial endothelial cells. Preclinical studies have demonstrated that VTB-10 can reverse abnormal vascular remodeling and restore functional endothelium, thereby normalizing pulmonary artery structure and function[1][2][4][6][8].
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 VTB-10.