A Study to Evaluate Efficacy and Safety of Oral BAY63-2521 in Patients With CTEPH. - NCT00855465-30030 (Clinical Trial 275644)


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A Study to Evaluate Efficacy and Safety of Oral BAY63-2521 in Patients With CTEPH. - NCT00855465-30030 (Clinical Trial 275644)
Permalink: http://www.ClinicalConnection.com/exp/ExpandedPatientViewStudy275644.aspx

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City:

Decatur

State:

Zip Code:

30030

Conditions:

Pulmonary Hypertension

Purpose:

The aim of the study is to assess the efficacy and safety of different doses of BAY63-2521, given orally for 16 weeks, in patients with Chronic Thromboembolic Pulmonary Hypertension (CTEPH).

Study summary:

Criteria:

Inclusion Criteria: - Male and female patients with CTEPH either inoperable or with persistent or recurrent PH after surgery. Exclusion Criteria: - All types of pulmonary hypertension except subtypes 4.1 and 4.2 of the Venice Clinical Classification of Pulmonary Hypertension.

Study is available at:

Decatur, GA 30030
United States

Primary Contact:
Bayer Clinical Trials Contact
Email: clinical-trials-contact@bayerhealthcare.com

If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.

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Data Source:		ClinicalTrials.gov
Date Processed:		March 16, 2010
Modifications to this listing:		Only selected fields are shown, please use the link above to view all information about this clinical trial.

Clinical trials are medical research studies designed to test the safety and/or effectiveness of new drugs, devices, or treatments in humans. These studies are conducted worldwide for a range of conditions and illnesses. Learn more about clinical research and participating in a study at About Clinical Trials.


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