Drug intelligence / Profile preview

PH-501

Development stage
Unknown
Lead developer
Yuanyan Pharmaceutical Port Life Science Research
Modality
Small Molecules
Administration
Oral
01

Overview

PH-501 is an orally administered small molecule phosphodiesterase type 5 (PDE5) inhibitor being developed for the treatment of pulmonary arterial hypertension (PAH). Developed by Original Drug Port (Shanghai) Pharmaceutical, the compound targets the PDE5 enzyme to prevent the degradation of cyclic guanosine monophosphate (cGMP) in pulmonary vascular smooth muscle cells. Increased cGMP levels facilitate vasodilation and inhibit the proliferation of smooth muscle cells, thereby reducing pulmonary arterial pressure and improving exercise capacity. PH-501 is currently being evaluated in a Phase Ib/II clinical trial (CTR20252910) in China to determine its safety, pharmacokinetics, and preliminary efficacy in patients with PAH.

02

Targets

PDE5 (Phosphodiesterase 5A)

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