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Hypertension, PulmonaryPhase 2LEPHTNCT01065454

A Study to Test the Effects of Riociguat in Patients With Pulmonary Hypertension Associated With Left Ventricular Systolic Dysfunction

A Phase 2 study testing Riociguat (Adempas, BAY63-2521) in people with Hypertension, Pulmonary and Ventricular Dysfunction, Left, run by Bayer at 83 sites in 18 countries.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record

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Trial summary

The aim of this study is to assess whether increasing oral doses of Riociguat are safe and improve the well-being, symptoms and outcome in patients with pulmonary hypertension associated with left ventricular systolic dysfunction Read more about this study

Who is it for?
Ages 18 to 80 years
What is being tested?
Riociguat (Adempas, BAY63-2521)
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
202 participants
Where
83 sitesin 18 countries
Study dates
14 Apr 2010to 23 Jul 2025
Phase
Phase 2

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Male and female patients with symptomatic pulmonary hypertension due to left ventricular systolic dysfunction despite optimized heart failure therapy

Who cannot join

  • Types of pulmonary hypertension other than group 2.1 of Dana Point Classification

Trial locations and contacts

83 sites in 18 countries.

83 sites in 18 countries

United States14 sites
  • Study site

    Baltimore, Maryland, 21201

  • Study site

    Boston, Massachusetts, 02114-2696

  • Study site

    Cincinnati, Ohio, 45219

  • Study site

    Fairfield, Ohio, 45014

  • Study site

    Falls Church, Virginia, 22042

  • Study site

    Iowa City, Iowa, 52242

  • Study site

    Los Angeles, California, 90073-1003

  • Study site

    Miami, Florida, 33136

  • Study site

    Milwaukee, Wisconsin, 53215

  • Study site

    Rochester, Minnesota, 55905

  • Study site

    San Diego, California, 92103

  • Study site

    St Louis, Missouri, 63110

  • Study site

    Torrance, California, 90502

  • Study site

    Westminster, California, 92683

Other trials in United States

Japan14 sites
  • Study site

    Arakawa-ku, Tokyo, 116-8567

  • Study site

    Higashiibaraki, Ibaraki, 311-3193

  • Study site

    Kita-ku, Osaka, Osaka, 530-8480

  • Study site

    Kusatsu, Shiga, 525-8585

  • Study site

    Nagoya, Aichi-ken, 466-8560

  • Study site

    Ōgaki, Gifu, 503-8502

  • Study site

    Osaka, Osaka, 541-8567

  • Study site

    Sendai, Miyagi, 980-8574

  • Study site

    Seto, Aichi-ken, 489-8642

  • Study site

    Shinjuku-ku, Tokyo, 162-8666

  • Study site

    Suita, Osaka, 565-0871

  • Study site

    Sunto, Shizuoka, 411-8611

  • Study site

    Tanabe, Wakayama, 646-8558

  • Study site

    Tsu, Mie-ken, 514-1101

Other trials in Japan

Spain7 sites
  • Study site

    A Coruña, A Coruña, 15006

  • Study site

    Barcelona, Barcelona, 08003

  • Study site

    Madrid, Madrid, 28041

  • Study site

    Majadahonda, Madrid, 28222

  • Study site

    Murcia, Murcia, 30120

  • Study site

    Palma, Palma de Mallorca, 7198

  • Study site

    Valencia, Valencia, 46026

Other trials in Spain

France6 sites
  • Study site

    Bron, 69677

  • Study site

    Lille, 59037

  • Study site

    Nantes, 44035

  • Study site

    Pessac, 33604

  • Study site

    Rouen, 76031

  • Study site

    Toulouse, 31059

Other trials in France

Germany5 sites
  • Study site

    Augsburg, Bavaria, 86156

  • Study site

    Cologne, North Rhine-Westphalia, 50937

  • Study site

    Erfurt, Thuringia, 99089

  • Study site

    Greifswald, Mecklenburg-Vorpommern, 17475

  • Study site

    Heidelberg, Baden-Wurttemberg, 69115

Other trials in Germany

Belgium4 sites
  • Study site

    Aalst, 9300

  • Study site

    Brussels, 1070

  • Study site

    Ghent, 9000

  • Study site

    Leuven, 3000

Other trials in Belgium

Canada4 sites
  • Study site

    Edmonton, Alberta, T6G 2B7

  • Study site

    Montreal, Quebec, H3T 1E2

  • Study site

    Québec, Quebec, G1V 4G5

  • Study site

    Vancouver, British Columbia, V5Z 1M9

Other trials in Canada

Czechia4 sites
  • Study site

    Brno, 656 91

  • Study site

    Olomouc, 77900

  • Study site

    Prague, 12808

  • Study site

    Prague, 140 21

Other trials in Czechia

Australia3 sites
  • Study site

    Herston, Queensland, 4029

  • Study site

    Melbourne, Victoria, 3004

  • Study site

    Sydney, New South Wales, 2010

Other trials in Australia

China3 sites
  • Study site

    Beijing, 100020

  • Study site

    Shanghai, 200032

  • Study site

    Shanghai, 200433

Other trials in China

Netherlands3 sites
  • Study site

    Amsterdam, 1081 HV

  • Study site

    Amsterdam, 1091 AC

  • Study site

    Nijmegen, 6525 GA

Other trials in Netherlands

Poland3 sites
  • Study site

    Bydgoszcz, 85-168

  • Study site

    Gdansk, 80-214

  • Study site

    Warsaw, 04-628

Other trials in Poland

Singapore3 sites
  • Study site

    Singapore, 119074

  • Study site

    Singapore, 169609

  • Study site

    Singapore, 308433

Other trials in Singapore

Switzerland3 sites
  • Study site

    Geneva, Canton of Geneva, 1205

  • Study site

    Lugano, Canton Ticino, 6900

  • Study site

    Zurich, Canton of Zurich, 8091

Other trials in Switzerland

Austria2 sites
  • Study site

    Innsbruck, Tyrol, 6020

  • Study site

    Vienna, State of Vienna, 1090

Other trials in Austria

Italy2 sites
  • Study site

    Naples, Campania, 80131

  • Study site

    Pavia, Lombardy, 27100

Other trials in Italy

United Kingdom2 sites
  • Study site

    Cambridge, Cambridgeshire, CB2 0AY

  • Study site

    London, London, SW3 6NP

Other trials in United Kingdom

Denmark1 site
  • Study site

    Aarhus N, 8200

Other trials in Denmark

About this study

Official title: Randomized, Double Blind, Placebo Controlled, Parallel Group, Multi-center Study to Evaluate the Hemodynamic Effects of Riociguat (BAY 63-2521) as Well as Safety and Kinetics in Patients With Pulmonary Hypertension Associated With Left Ventricular Systolic Dysfunction

The aim of this study is to assess whether increasing oral doses of Riociguat are safe and improve the well-being, symptoms and outcome in patients with pulmonary hypertension associated with left ventricular systolic dysfunction

Read the detailed description

Pharmacokinetics parameters were regarded as exploratory parameters. Adverse event data will be covered in Adverse events section.

Being tested
Riociguat (Adempas, BAY63-2521), Placebo
Keywords
Pulmonary Hypertension, Left ventricular dysfunction
Medical subject headings
Hypertension, Pulmonary, Ventricular Dysfunction, Left

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Riociguat (Adempas, BAY63-2521)Drug

    up to 2 mg three times a day (increasing from 0.5 to 1 to 2 mg)

  • Riociguat (Adempas, BAY63-2521)Drug

    up to 1 mg three times a day (increasing from 0.5 to 1 mg)

  • Riociguat (Adempas, BAY63-2521)Drug

    fixed 0.5 mg three times a day

  • PlaceboDrug

    Placebo three times a day

Study groups in NCT01065454
Study groupRoleWhat they receive
Riociguat (Adempas, BAY63-2521) up to 2 mgExperimentalParticipants received riociguat up to 2 mg three times per day (tid) (increasing from 0.5 to 1 to 2 mg).
Receives: Drug: Riociguat (Adempas, BAY63-2521)
Riociguat (Adempas, BAY63-2521) up to 1 mgExperimentalParticipants received riociguat up to 1 mg tid (increasing from 0.5 to 1 mg).
Receives: Drug: Riociguat (Adempas, BAY63-2521)
Riociguat (Adempas, BAY63-2521) fixed 0.5 mgExperimentalParticipants received riociguat 0.5 mg tid (fixed dose).
Receives: Drug: Riociguat (Adempas, BAY63-2521)
PlaceboPlacebo comparatorParticipants received placebo tid.
Receives: Drug: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Pulmonary Artery Mean Pressure (PAPmean) at Rest - Change From Baseline to Week 16

    Mean pulmonary arterial pressure (PAPmean) is a directly measured hemodynamic parameter. PAPmean is recorded during a right heart catheterization.

    Measured: Baseline and visit 6 (16 weeks)

Secondary outcomes (25)
  1. Venous Oxygen Saturation (SvO2) - Change From Baseline to Week 16

    The mixed venous oxygen saturation rate (SvO2) is a directly measured hemodynamic parameter. SvO2 is recorded during a right heart catheterization.

    Measured: Baseline and visit 6 (16 weeks)

  2. Pulmonary Vascular Resistance (PVR) - Change From Baseline to Week 16

    The pulmonary vascular resistance (PVR) is a calculated hemodynamic parameter. PVR is derived from the directly measured parameters mean pulmonary arterial pressure (PAPmean) and pulmonary capillary wedge pressure (PCWP), divided by the cardiac output (CO). PVR and PAPmean are acquired during a right heart catheterization. CO is a calculated hemodynamic parameter, too. Formula: PVR = 80*(PAPmean - PCWP)/CO

    Measured: Baseline and visit 6 (16 weeks)

  3. Pulmonary Vascular Resistance Index (PVRi) - Change From Baseline to Week 16

    The pulmonary vascular resistance index (PVRi) is a calculated hemodynamic parameter. PVRi is derived from the pulmonary vascular resistance (PVR) normalized by the body surface area (BSA). Formula: PVRi = 80*(PAPmean - PCWP)*BSA/CO

    Measured: Baseline and visit 6 (16 weeks)

  4. Systemic Vascular Resistance (SVR) - Change From Baseline to Week 16

    The systemic vascular resistance (SVR) is a calculated hemodynamic parameter. SVR is derived from the directly measured parameter mean right atrial pressure (RAPmean) and the calculated parameter mean systemic arterial pressure (SAPmean) divided by the cardiac output (CO). RAPmean is acquired during a right heart catheterization. CO is a calculated hemodynamic parameter, too. Formula: SVR = 80*(SAPmean - RAPmean)/CO

    Measured: Baseline and visit 6 (16 weeks)

  5. Systemic Vascular Resistance Index (SVRi) - Change From Baseline to Week 16

    The systemic vascular resistance index (SVRi) is a calculated hemodynamic parameter. SVRi is derived from the systemic vascular resistance (SVR) normalized by the body surface area (BSA). Formula: SVRi = 80*(SAPmean - RAPmean)*BSA/CO

    Measured: Baseline and visit 6 (16 weeks)

  6. Transpulmonary Pressure Gradient (TPG) - Change From Baseline to Week 16

    The transpulmonary pressure gradient (TPG) is a calculated hemodynamic parameter. TPG is calculated from the directly measured parameters mean pulmonary arterial pressure (PAPmean) and pulmonary capillary wedge pressure (PCWP). These 2 parameters are acquired during a right heart catheterization. Formula: TPG = PAPmean - PCWP

    Measured: Baseline and visit 6 (16 weeks)

  7. Pulmonary Capillary Wedge Pressure (PCWP) - Change From Baseline to Week 16

    Pulmonary capillary wedge pressure (PCWP) is a directly measured hemodynamic parameter acquired during a right heart catheterization.

    Measured: Baseline and visit 6 (16 weeks)

  8. Tricuspid Annular Plane Systolic Excursion (TAPSE) - Change From Baseline to Week 16

    The tricuspid annular plane systolic excursion (TAPSE) is a measured echocardiography parameter. It is acquired during a non-invasive echocardiography examination.

    Measured: Baseline and visit 6 (16 weeks)

  9. Systolic Pulmonary Arterial Pressure (PAPsyst) - Change From Baseline to Week 16

    Systolic pulmonary arterial pressure (PAPsyst) is a directly measured hemodynamic parameter acquired during a right heart catheterization.

    Measured: Baseline and visit 6 (16 weeks)

  10. Left Ventricular Ejection Fraction (LVEF) - Change From Baseline to Week 16

    The left ventricular ejection fraction work index (LVEF) is a calculated echocardiography parameter. LVEF is derived from the directly measured parameters left ventricular end-diastolic volume (LVEDV) and left ventricular end-systolic volume (LVESV). These 2 parameters are acquired during a non-invasive echocardiography examination. Formula: LEVF = 100*(LVEDV - LVESV)/LVEDV

    Measured: Baseline and visit 6 (16 weeks)

  11. Left Ventricular End-systolic Volume (LVESV) - Change From Baseline to Week 16

    Left ventricular end-systolic volume (LVESV) is a measured echocardiography parameter. It is acquired during a non-invasive echocardiography examination.

    Measured: Baseline and visit 6 (16 weeks)

  12. Left Ventricular End-diastolic Volume (LVEDV) - Change From Baseline to Week 16

    Left ventricular end-diastolic volume (LVEDV) is a measured echocardiography parameter. It is acquired during a non-invasive echocardiography examination.

    Measured: Baseline and visit 6 (16 weeks)

  13. E-wave Deceleration Time - Change From Baseline to Week 16

    E-wave deceleration time is a measured echocardiography parameter. It is acquired during a non-invasive echocardiography examination.

    Measured: Baseline and visit 6 (16 weeks)

  14. Ratio of Mitral Peak Velocity of Early Filling to Mitral Peak Velocity of Late Filling (E/A) - Change From Baseline to Week 16

    E/A ratio is a measured echocardiography parameter and describes the ratio of mitral peak velocity of early filling to mitral peak velocity of late filling. It is acquired during a non-invasive echocardiography examination.

    Measured: Baseline and visit 6 (16 weeks)

  15. 6-minute Walking Distance (6MWD) - Change From Baseline to Week 16

    6-minute walking distance (6MWD) is a measure for the objective evaluation of a patient's functional exercise capacity.

    Measured: Baseline and visit 6 (16 weeks)

  16. WHO (World Health Organization) Functional Class - Change From Baseline to Week 16

    The WHO functional assessment of pulmonary arterial hypertension ranged from functional class I (Patients with PH but without resulting limitation of physical activity) to class IV (Patients with PH with inability to carry out any physical activity without symptoms. These patients manifest signs of right-heart failure.). Changes to a lower WHO functional class resemble improvement, changes to a higher functional class resemble deterioration of PAH.

    Measured: Baseline and visit 6 (16 weeks)

  17. Percentage of Participants With Clinical Worsening

    The combined endpoint "time to clinical worsening", made up of the following components, defined by the first occurrence: all cause mortality, including cardiovascular mortality; first hospitalization for a cardiovascular event, including heart failure, acute myocardial infarction, stroke or ventricular arrhythmia; upgrade of the HTx (heart transplantation) status to next higher level; need for IV diuretics; persistent worsening of WHO functional class due to deterioration of PH or cardiac function.

    Measured: At visit 6 (16 weeks)

  18. Borg CR 10 Scale - Change From Baseline to Week 16

    The Borg CR10 Scale is a patient reported outcome measure used in clinical diagnosis of e.g. breathlessness and dyspnea. It documents the patient's exertion during a physical test. Low values indicate low levels of exertion, high values indicate more intense exertion reported by the patient. The score ranges from 0 ("Nothing at all") to 10 ("Extremely strong - Maximal").

    Measured: Baseline and visit 6 (16 weeks)

  19. EQ-5D Utility Score - Change From Baseline to Week 16

    EQ-5D utility score is a Quality-of-Life patient reported outcome measure. An increase in the utility score represents an improvement in quality of life. The score ranges from 0 (worst imaginable health state) to 100 (best imaginable health state).

    Measured: Baseline and visit 6 (16 weeks)

  20. Minnesota Living With Heart Failure Questionnaire (MLHF) Score - Change From Baseline to Week 16

    The self-reported Minnesota Living with Heart Failure questionnaire (MLHF) is designed to measure the effects of PH and PH-specific treatments on an individual's quality of life. The MLHF total score can range from 0 (best) to 105 (worst).

    Measured: Baseline and visit 6 (16 weeks)

  21. Cystatin C - Change From Baseline to Week 16

    Cystatin C is a biomarker for predicting new onset or deteriorating cardiovascular disease.

    Measured: Baseline and visit 6 (16 weeks)

  22. N-terminal Pro-brain Natriuretic Peptide (NT-pro BNP) - Change From Baseline to Week 16

    N-terminal pro-brain natriuretic peptide (NT-pro BNP) levels in the blood are used for screening, diagnosis of acute congestive heart failure (CHF) and may be useful to establish prognosis in heart failure.

    Measured: Baseline and visit 6 (16 weeks)

  23. Troponin T - Change From Baseline to Week 16

    Troponin T is a cardiac-specific protein which is released from damaged or injured heart muscle cells.

    Measured: Baseline and visit 6 (16 weeks)

  24. Asymmetric Dimethylarginine (ADMA) - Change From Baseline to Week 16

    Asymmetric dimethylarginine (ADMA) is an endogenous inhibitor of nitric oxides. Recent clinical studies have indicated that ADMA may have diagnostic relevance as a novel cardiovascular risk marker.

    Measured: Baseline and visit 6 (16 weeks)

  25. Osteopontin - Change From Baseline to Week 16

    Osteopontin is a cytokine-like pro-fibrotic mediator, which is expressed in cardiovascular tissues. Its expression is induced by increased pressure and volume load in the myocardium, kidney and lung. Therefore, osteopontin may be used as a prognostic marker in patients with cardiovascular diseases.

    Measured: Baseline and visit 6 (16 weeks)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Feb 2010 (estimated)
  2. Study start14 Apr 2010
  3. Primary completion6 Jun 2012
  4. Study completion23 Jul 2025

Why it stopped: The sponsor terminated the study for strategic reasons. This decision was not due to safety concerns for participants receiving treatment at the time the study was terminated.

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
202 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01065454
Sponsor's protocol ID
14308
Other IDs
2023-507001-34-00, 2009-015878-35, 2009, 2023
Acronym
LEPHT
Status last verified
Aug 2026
First submitted
8 Feb 2010
Last updated
20 Aug 2026
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
No: Availability of this study's data will later be determined according to Bayer's commitment to the EFPIA/PhRMA "Principles for responsible clinical trial data sharing". This pertains to scope, timepoint and process of data access. As such, Bayer commits to sharing upon request from qualified researchers patient-level clinical trial data, study-level clinical trial data, and protocols from clinical trials in patients for medicines and indications approved in the US and EU as necessary for conducting legitimate research. This applies to data on new medicines and indications that have been approved by the EU and US regulatory agencies on or after January 01, 2014. Interested researchers can use www.vivli.org to request access to anonymized patient-level data and supporting documents from clinical studies to conduct research. Information on the Bayer criteria for listing studies and other relevant information is provided in the member section of the portal.

Publications

  • Ghio S, Bonderman D, Felix SB, Ghofrani HA, Michelakis ED, Mitrovic V, Oudiz RJ, Frey R, Roessig L, Semigran MJ. Left ventricular systolic dysfunction associated with pulmonary hypertension riociguat trial (LEPHT): rationale and design. Eur J Heart Fail. 2012 Aug;14(8):946-53. doi: 10.1093/eurjhf/hfs071. Epub 2012 Jun 20.

    PubMed 22719060
  • Bonderman D, Ghio S, Felix SB, Ghofrani HA, Michelakis E, Mitrovic V, Oudiz RJ, Boateng F, Scalise AV, Roessig L, Semigran MJ; Left Ventricular Systolic Dysfunction Associated With Pulmonary Hypertension Riociguat Trial (LEPHT) Study Group. Riociguat for patients with pulmonary hypertension caused by systolic left ventricular dysfunction: a phase IIb double-blind, randomized, placebo-controlled, dose-ranging hemodynamic study. Circulation. 2013 Jul 30;128(5):502-11. doi: 10.1161/CIRCULATIONAHA.113.001458. Epub 2013 Jun 17.

    PubMed 23775260

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