View Clinical Trial (Medical Research Study)
A Study to Evaluate Efficacy and Safety of Oral BAY63-2521 in Patients With CTEPH. - NCT00855465-(Clinical Trial 275645)
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Baltimore |
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MD |
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| Conditions: |
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Pulmonary Hypertension |
| Purpose: |
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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).
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| Study summary: |
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| Criteria: |
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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. |
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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: |
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ClinicalTrials.gov |
| Date Processed: |
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June 22, 2010 |
Modifications to
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Only selected fields are shown, please use the link
above to view all information about this clinical trial. |
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