Can a Lung-Blood-Pressure drug ease the strain of heart failure?
NCT ID NCT01065454
First seen Aug 20, 2026 · Last updated Aug 21, 2026 · Updated 1 time
Summary
This trial tests whether riociguat, a drug that relaxes blood vessels in the lungs, can safely lower high blood pressure in the lungs of people who also have a weakened left heart chamber. Participants receive either riociguat or a placebo for 16 weeks, with doctors measuring lung artery pressure and oxygen levels via a heart catheter. The goal is to see if the drug improves symptoms and well-being in this specific group of patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- riociguat (Adempas)
- What this could lead to
- If it works, riociguat could offer a new way to lower blood pressure in the lungs and ease symptoms for people with heart failure-related pulmonary hypertension.
- What could go wrong
- This is an early-phase trial, so the drug may not prove effective or safe in this specific patient group. Possible side effects include low blood pressure and bleeding risk.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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202 people
The number who actually took part.
- Started
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Apr 2010
- Finished
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Jul 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 80 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Male and female patients with symptomatic pulmonary hypertension due to left ventricular systolic dysfunction despite optimized heart failure therapy Exclusion Criteria: * Types of pulmonary hypertension other than group 2.1 of Dana Point Classification
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Study site
Los Angeles, California, 90073-1003, United States
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Study site
San Diego, California, 92103, United States
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Torrance, California, 90502, United States
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Westminster, California, 92683, United States
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Miami, Florida, 33136, United States
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Iowa City, Iowa, 52242, United States
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Baltimore, Maryland, 21201, United States
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Boston, Massachusetts, 02114-2696, United States
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Rochester, Minnesota, 55905, United States
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St Louis, Missouri, 63110, United States
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Cincinnati, Ohio, 45219, United States
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Fairfield, Ohio, 45014, United States
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Falls Church, Virginia, 22042, United States
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Milwaukee, Wisconsin, 53215, United States
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Sydney, New South Wales, 2010, Australia
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Herston, Queensland, 4029, Australia
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Melbourne, Victoria, 3004, Australia
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Vienna, State of Vienna, 1090, Austria
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Innsbruck, Tyrol, 6020, Austria
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Aalst, 9300, Belgium
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Brussels, 1070, Belgium
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Ghent, 9000, Belgium
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Leuven, 3000, Belgium
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Edmonton, Alberta, T6G 2B7, Canada
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Vancouver, British Columbia, V5Z 1M9, Canada
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Montreal, Quebec, H3T 1E2, Canada
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Québec, Quebec, G1V 4G5, Canada
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Beijing, 100020, China
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Shanghai, 200032, China
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Shanghai, 200433, China
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Brno, 656 91, Czechia
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Olomouc, 77900, Czechia
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Prague, 12808, Czechia
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Prague, 140 21, Czechia
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Aarhus N, 8200, Denmark
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Bron, 69677, France
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Lille, 59037, France
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Nantes, 44035, France
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Pessac, 33604, France
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Rouen, 76031, France
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Toulouse, 31059, France
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Heidelberg, Baden-Wurttemberg, 69115, Germany
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Augsburg, Bavaria, 86156, Germany
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Greifswald, Mecklenburg-Vorpommern, 17475, Germany
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Cologne, North Rhine-Westphalia, 50937, Germany
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Erfurt, Thuringia, 99089, Germany
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Naples, Campania, 80131, Italy
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Pavia, Lombardy, 27100, Italy
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Nagoya, Aichi-ken, 466-8560, Japan
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Seto, Aichi-ken, 489-8642, Japan
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Study site
Ōgaki, Gifu, 503-8502, Japan
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Higashiibaraki, Ibaraki, 311-3193, Japan
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Study site
Tsu, Mie-ken, 514-1101, Japan
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Study site
Sendai, Miyagi, 980-8574, Japan
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Study site
Kita-ku, Osaka, Osaka, 530-8480, Japan
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Osaka, Osaka, 541-8567, Japan
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Suita, Osaka, 565-0871, Japan
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Study site
Kusatsu, Shiga, 525-8585, Japan
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Study site
Sunto, Shizuoka, 411-8611, Japan
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Study site
Arakawa-ku, Tokyo, 116-8567, Japan
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Study site
Shinjuku-ku, Tokyo, 162-8666, Japan
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Tanabe, Wakayama, 646-8558, Japan
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Amsterdam, 1081 HV, Netherlands
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Amsterdam, 1091 AC, Netherlands
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Nijmegen, 6525 GA, Netherlands
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Bydgoszcz, 85-168, Poland
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Gdansk, 80-214, Poland
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Warsaw, 04-628, Poland
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Singapore, 119074, Singapore
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Study site
Singapore, 169609, Singapore
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Study site
Singapore, 308433, Singapore
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Study site
A Coruña, A Coruña, 15006, Spain
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Study site
Barcelona, Barcelona, 08003, Spain
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Study site
Madrid, Madrid, 28041, Spain
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Study site
Majadahonda, Madrid, 28222, Spain
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Murcia, Murcia, 30120, Spain
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Palma, Palma de Mallorca, 7198, Spain
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Study site
Valencia, Valencia, 46026, Spain
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Study site
Geneva, Canton of Geneva, 1205, Switzerland
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Zurich, Canton of Zurich, 8091, Switzerland
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Study site
Lugano, Canton Ticino, 6900, Switzerland
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Study site
Cambridge, Cambridgeshire, CB2 0AY, United Kingdom
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Study site
London, London, SW3 6NP, United Kingdom
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