Trials / Terminated
TerminatedNCT01172756
A Study to Test the Effects of Riociguat in Patients With Pulmonary Hypertension Associated With Left Ventricular Diastolic Dysfunction
Acute Hemodynamic Effects of Riociguat (BAY63-2521) in Patients With Pulmonary Hypertension Associated With Diastolic Heart Failure: A Randomized, Double-blind, Placebo-controlled, Single-dose Study in Three Ascending Dose Cohorts
- Status
- Terminated
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 39 (actual)
- Sponsor
- Bayer · Industry
- Sex
- All
- Age
- 18 Years – 90 Years
- Healthy volunteers
- Not accepted
Summary
The aim of this study is to assess whether single oral doses of Riociguat safely improve the cardiovascular function in patients with pulmonary hypertension associated with left ventricular diastolic dysfunction
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Riociguat (BAY63-2521) | 0.5 mg single oral dose |
| DRUG | Riociguat (BAY63-2521) | 1 mg single oral dose |
| DRUG | Riociguat (BAY63-2521) | 2 mg single oral dose |
| DRUG | Placebo | single oral dose |
Timeline
- Start date
- 2010-07-01
- Primary completion
- 2012-10-01
- Completion
- 2012-10-01
- First posted
- 2010-07-30
- Last updated
- 2014-11-04
Locations
7 sites across 3 countries: Austria, Czechia, Germany
Source: ClinicalTrials.gov record NCT01172756. Inclusion in this directory is not an endorsement.