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Riociguat in Patients With Chronic Thromboembolic Pulmonary Hypertension (CTEPH) — EAS  

Hypertension, Pulmonary Clinical Trial

Official title:
An Open-label Phase IIIb Study of Riociguat in Patients With In-operable CTEPH, or Recurrent or Persisting PH After Surgical Treatment Who Are Not Satisfactorily Treated and Cannot Participate in Any Other CTEPH Trial

Clinical Trial Summary

The aim of the study is to assess safety, tolerability and clinical effects of different doses of riociguat in patients with inoperable Chronic Thromboembolic Pulmonary Hypertension (CTEPH) and who are not satisfactorily treated and cannot participate in any other CTEPH trial. In the US the study runs as an Expanded Access program under 21 CFR 312.320.

Clinical Trial Description

n/a

Study Design

N/A

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01784562
Study type Expanded Access
Source Bayer
Contact
Status No longer available
Phase N/A
View Details
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