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.
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
- Conditions the study is for
- Hypertension, Pulmonary, Ventricular Dysfunction, Left
- 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
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
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
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
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
Belgium4 sites
Study site
Aalst, 9300
Study site
Brussels, 1070
Study site
Ghent, 9000
Study site
Leuven, 3000
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
Czechia4 sites
Study site
Brno, 656 91
Study site
Olomouc, 77900
Study site
Prague, 12808
Study site
Prague, 140 21
Australia3 sites
Study site
Herston, Queensland, 4029
Study site
Melbourne, Victoria, 3004
Study site
Sydney, New South Wales, 2010
China3 sites
Study site
Beijing, 100020
Study site
Shanghai, 200032
Study site
Shanghai, 200433
Netherlands3 sites
Study site
Amsterdam, 1081 HV
Study site
Amsterdam, 1091 AC
Study site
Nijmegen, 6525 GA
Poland3 sites
Study site
Bydgoszcz, 85-168
Study site
Gdansk, 80-214
Study site
Warsaw, 04-628
Singapore3 sites
Study site
Singapore, 119074
Study site
Singapore, 169609
Study site
Singapore, 308433
Switzerland3 sites
Study site
Geneva, Canton of Geneva, 1205
Study site
Lugano, Canton Ticino, 6900
Study site
Zurich, Canton of Zurich, 8091
Austria2 sites
Study site
Innsbruck, Tyrol, 6020
Study site
Vienna, State of Vienna, 1090
Italy2 sites
Study site
Naples, Campania, 80131
Study site
Pavia, Lombardy, 27100
United Kingdom2 sites
Study site
Cambridge, Cambridgeshire, CB2 0AY
Study site
London, London, SW3 6NP
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 group | Role | What they receive |
|---|---|---|
| Riociguat (Adempas, BAY63-2521) up to 2 mg | Experimental | Participants 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 mg | Experimental | Participants 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 mg | Experimental | Participants received riociguat 0.5 mg tid (fixed dose). Receives: Drug: Riociguat (Adempas, BAY63-2521) |
| Placebo | Placebo comparator | Participants received placebo tid. Receives: Drug: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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.
- First posted9 Feb 2010 (estimated)
- Study start14 Apr 2010
- Primary completion6 Jun 2012
- 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
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Hypertension, PulmonaryStudies of the same condition, open and under way.
- More trials run by BayerThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Bayer
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Bayer Study Director, Study director, Bayer
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
- Results posted
- Yes, on ClinicalTrials.gov
- 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 22719060Bonderman 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