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Clinical 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


Clinical Trial Description

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


Study Design


Related Conditions & MeSH terms


NCT number NCT01065454
Study type Interventional
Source Bayer
Contact
Status Active, not recruiting
Phase Phase 2
Start date April 14, 2010
Completion date December 31, 2025

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