A Study to Evaluate Efficacy & Safety of Oral BAY63-2521 in Patients With

Clinical Trial Description

Adverse event data will be covered in Adverse events section. ;

Study Design

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NCT number	NCT00855465
Study type	Interventional
Source	Bayer
Contact
Status	Completed
Phase	Phase 3
Start date	February 23, 2009
Completion date	June 27, 2012

A Study to Evaluate Efficacy and Safety of Oral BAY63-2521 in Patients With CTEPH. — CHEST-1

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms