Idiopathic Interstitial Pneumonias / Hypertension,Pulmonary Clinical Trial
— RISE-IIPOfficial 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).
| Verified date | October 2017 |
| Source | Bayer |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
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).
| Status | Terminated |
| Enrollment | 147 |
| Est. completion date | September 14, 2016 |
| Est. primary completion date | May 5, 2016 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 80 Years |
| Eligibility |
- Inclusion Criteria: - Men or women aged from =18 to =80 years - Diagnosed with one of the following (confirmed using a multidisciplinary approach, as per ATS(American Thoracic Society) / ERS(European Respiratory Society) / JRS (Japanese Respiratory Society) / ALAT(Latin American Thoracic Association) guidelines: - Major IIPs (idiopathic interstitial pneumonias) diagnosis or suspected as one of the following: - Idiopathic pulmonary fibrosis - Idiopathic nonspecific interstitial pneumonia - Respiratory bronchiolitis-interstitial lung disease - Desquamative interstitial pneumonia - Cryptogenic organizing pneumonia - Acute interstitial pneumonia - Rare IIPs diagnosis by one of the following: - Idiopathic lymphoid interstitial pneumonia - Idiopathic pleuroparenchymal fibroelastosis - Unclassifiable idiopathic interstitial pneumonias - Forced Vital Capacity (FVC) = 45 % - 6MWD (6 minutes walking distance) = 150 m to = 450 m {under stable O2(oxygen) supplementation via nasal cannula} - Diagnosis of PH (pulmonary hypertension) confirmed by right heart catheter (RHC) with (mean artery pulmonary artery pressure )mPAP = 25 mmHg and (pulmonary artery wedge pressure)PAWP =15 mmHg at rest - Systolic blood pressure (SBP) = 95 mmHg and no signs or symptoms of hypotension - WHO functional class II-IV - Women of childbearing potential can only be included in the study if a pregnancy test is negative. Women of childbearing potential must agree to use adequate contraception when sexually active. 'Adequate contraception' is defined as any combination of at least 2 effective methods of birth control, of which at least one is a physical barrier (e.g. condoms with hormonal contraception or implants or combined oral contraceptives, certain intrauterine devices). Adequate contraception is required from the signing of the informed consent form up until 4 weeks after the last study drug administration - Exclusion Criteria: - Known significant left heart disease: - Pulmonary venous hypertension indicated by baseline pulmonary capillary wedge pressure > 15 mmHg - Symptomatic coronary artery disease - Systolic left-ventricular dysfunction with an left ventricular ejection fraction (LVEF) <45% - Active state of hemoptysis or pulmonary hemorrhage, including those events managed by bronchial artery embolization - Any history of bronchial artery embolization or massive hemoptysis within 3 months prior to screening. Massive hemoptysis being defined as acute bleeding >240 mL in a 24-hour period or recurrent bleeding >100 mL/d over several days - Difference > 15% between the eligibility and the baseline 6MWD test - Forced expiratory volume in one second (FEV1) / Forced Vital Capacity (FVC) <0.65 after bronchodilator administration - Initiation in cytotoxic, immunosuppressive, cytokine modulating therapy initiated within 3 months prior to screening. Such agents might include. azathioprine, cyclophosphamide, corticosteroids, etanercept, tumor necrosis factor alpha (TNFa) inhibitors and others - Any specific treatment for (pulmonary arterial hypertension) PAH/PH (pulmonary hypertension )within 3 months prior to screening - Concomitant use of the following medication: nitrates or (nitric oxide) NO donors (such as amyl nitrite) in any form, phosphodiesterase 5 inhibitors (such as sildenafil, tadalafil, vardenafil) and non-specific phosphodiesterase (PDE) inhibitors (theophylline, dipyridamole), - Pregnant women (i.e. positive pregnancy test or other signs of pregnancy), or breast feeding women, or women of childbearing potential not using adequate contraception (as defined in the aforementioned inclusion criterion) and not willing to agree to 4 weekly pregnancy testing from Visit 1(first administration of study drug) onwards until 4 weeks after last study drug intake |
| Country | Name | City | State |
|---|---|---|---|
| United States | University of California, Los Angeles | Los Angeles | California |
| United States | Columbia University Medical Center | New York | New York |
| United States | Via Christi Clinic | Wichita | Kansas |
| Lead Sponsor | Collaborator |
|---|---|
| Bayer |
United States, Argentina, Australia, Belgium, Canada, Colombia, Denmark, France, Germany, Greece, Israel, Italy, Japan, New Zealand, Portugal, Russian Federation, Saudi Arabia, Spain, Switzerland, Turkey, United Kingdom,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Mean Change in 6 Minute Walking Distance (6MWD) From Baseline to Week 26 | The 6MWD test is designed to evaluate a patient's exercise capacity while performing an everyday activity. | Baseline to 26 weeks | |
| Secondary | Number 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; need for hospitalization due to worsening cardiopulmonary (CP) status, attributable to progression of disease (including but not limited to increased shortness of breath or increased leg swelling); >15% decrease in the 6MWD test; worsening of WHO functional class. | From baseline to week 26 |