Phase 2Not yet recruiting

Clinical Trial of NS-863 in Participants With Pulmonary Arterial Hypertension (PAH)

A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Dose Finding Trial to Evaluate the Efficacy and Safety of Orally Administered NS-863 in Participants With Pulmonary Arterial Hypertension (PAH)

Sponsor
NS Pharma, Inc. (Industry)
Enrolment
135 planned
Conditions
Pulmonary Arterial Hypertension
Interventions
NS-863 Low Dose; NS-863 High Dose; NS-863 Placebo
Ages
adults, older adults
Registry
NCT07441200, CTIS2025-525114-38-00

Full record on ClinicalTrials.gov

From the registry

A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Dose Finding Trial to Evaluate the Efficacy and Safety of Orally Administered NS-863 in Participants with Pulmonary Arterial Hypertension (PAH)

Primary outcomes

  • Change in pulmonary vascular resistance (PVR) at week 24
  • Number of participants who experienced an adverse event (AE) up to approximately 24 weeks.

History

  1. Study completion expected

  2. Primary completion expected

  3. Started

  4. Registered