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Study to Evaluate Efficacy and Safety of JTT-251 in Participants With Pulmonary Arterial Hypertension — RELIEF-PAH  

Pulmonary Arterial Hypertension Clinical Trial

Official title:
A Phase 2, Multicenter, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of JTT-251 Administered for 24 Weeks to Participants With Pulmonary Arterial Hypertension (RELIEF-PAH)

Clinical Trial Summary

Study to evaluate the efficacy, safety, tolerability and pharmacokinetics of JTT-251 administered for 24 weeks in participants with pulmonary arterial hypertension (PAH)

Clinical Trial Description

This is a study to evaluate the efficacy, safety, tolerability and pharmacokinetics of JTT-251 administered for 24 weeks in participants with pulmonary arterial hypertension (PAH). Participants completing this study (RELIEF-PAH) will be eligible to enroll in an open-label extension study (RELIEF-PAH OLE) to evaluate the long-term efficacy, safety, tolerability and pharmacokinetics of JTT-251 in participants with PAH. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03789643
Study type Interventional
Source Akros Pharma Inc.
Contact
Status Withdrawn
Phase Phase 2
Start date March 2019
Completion date June 2021
View Details
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