Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
TPN171H is a novel, potent, and selective phosphodiesterase type 5 (PDE5) inhibitor developed for the treatment of pulmonary arterial hypertension (PAH) and erectile dysfunction (ED). As a small molecule drug, TPN171H acts by inhibiting PDE5A, leading to increased levels of cyclic guanosine monophosphate (cGMP), which promotes vasodilation in the pulmonary vasculature and corpus cavernosum. Clinical studies have shown that TPN171H is generally safe and well-tolerated in healthy subjects with linear pharmacokinetics over the tested dose range. Unlike some other PDE5 inhibitors, it has minimal impact on blood pressure or color discrimination. The drug has been approved for ED in Uzbekistan and is under regulatory review for ED in China; it remains under clinical development for PAH[1][2][3][4][5][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 TPN171H.