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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


NCT number NCT03789643
Study type Interventional
Source Akros Pharma Inc.
Contact Yoshiro Masuda
Phone 609-919-9570
Email ClinicalTrials@akrospharma.com
Status Not yet recruiting
Phase Phase 2
Start date March 2019
Completion date June 2021

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