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Terminated Phase 2 Interventional Results available

Efficacy and Safety of Riociguat in Patients With Symptomatic Pulmonary Hypertension (PH) Associated With Idiopathic Interstitial Pneumonias (IIP)

ClinicalTrials.gov ID: NCT02138825

Public ClinicalTrials.gov record NCT02138825. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 4:53 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-blind, Placebo-controlled Phase II Study to Investigate the Efficacy and Safety of Riociguat (0.5 mg, 1.0 mg, 1.5 mg, 2.0 mg and 2.5 mg TID) in Patients With Symptomatic Pulmonary Hypertension Associated With Idiopathic Interstitial Pneumonias (IIP).

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

To evaluate the efficacy and safety of 26-weeks of treatment with riociguat vs. placebo in patients with symptomatic PH (pulmonary hypertension) associated with IIP (idiopathic interstitial pneumonias).

Study identification

NCT ID
NCT02138825
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bayer
Industry
Enrollment
147 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 4, 2014 (Actual)
Primary completion
May 5, 2016 (Actual)
Completion
Sep 14, 2016 (Actual)
Last update posted
Dec 4, 2017

2014 – 2016

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
University of California, Los Angeles Los Angeles California 90024 —
Not listed San Francisco California 94143 —
Not listed Aurora Colorado 80045 —
Not listed Miami Florida 33136 —
Not listed Orlando Florida 32803 —
Via Christi Clinic Wichita Kansas 67208 —
Not listed Louisville Kentucky 40202 —
Columbia University Medical Center New York New York 10032 —
Not listed Durham North Carolina 27710 —
Not listed Cincinnati Ohio 45219 —
Not listed Cleveland Ohio 44195 —
Not listed Columbus Ohio 43221 —
Not listed Portland Oregon 97213 —
Not listed Pittsburgh Pennsylvania 15213 —
Not listed Nashville Tennessee 37232-5735 —
Not listed Dallas Texas 75235-3858 —
Not listed Falls Church Virginia 22042 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 76 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02138825, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 4, 2017 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02138825 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →