Long-term Safety and Efficacy of Ralinepag in Pulmonary Arterial Hypertension

Part of paid clinical trials in Birmingham, Alabama.

Sponsor
United Therapeutics
Study ID
NCT02279745
Phase
PHASE2
Status
Completed

Conditions

  • Pulmonary Arterial Hypertension

Eligibility Criteria

Sex
ALL
Age
18 Years - 75 Years
Healthy Volunteers
Not accepted

Interventions

Study Details

This study was an open-label extension study to determine the long-term safety and tolerability of ralinepag in subjects with World Health Organization (WHO) Group 1 pulmonary arterial hypertension (PAH) who have completed Study APD811-003, or who were assigned to receive placebo and were discontinued due to clinical worsening.

Key Dates

Start date
Jul 8, 2015
Status verified
Nov 2021
Primary completion
Mar 29, 2021
Completion
Mar 29, 2021

Study Design

Enrollment
45 participants (actual)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Oral Ralinepag
    Ralinepag immediate-release (IR) capsules of 10, 20, 30, 40, and 100 mcg or extended-release (XR) tablets of 50, 250, and 400 mcg for oral administration.

Primary Outcome Measure

Change From Baseline in Pulmonary Vascular Resistance [ Time Frame: At 1 or 2 years after the subject enrolled into the study, pending their last RHC prior to Protocol Amendment 2. ]

Locations (18)

Find similar trials in Birmingham, AL

Related Studies