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Sponsored by: |
Myogen |
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Information provided by: | Myogen |
ClinicalTrials.gov Identifier: | NCT00424021 |
AMB-220-E is an international, multicenter, open-label study examining the long-term safety of ambrisentan in subjects who have previously completed Myogen study AMB-220, "A Phase II, Randomized, Double-Blind, Dose-Controlled, Dose-Ranging, Multicenter Study of BSF 208075 Evaluating Exercise Capacity in Subjects with Moderate to Severe Pulmonary Arterial Hypertension".
Condition | Intervention | Phase |
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Pulmonary Hypertension |
Drug: ambrisentan |
Phase II |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Open Label, Dose Comparison, Single Group Assignment, Safety/Efficacy Study |
Official Title: | An Open-Label, Long-Term Study of Ambrisentan in Pulmonary Hypertension Subjects Having Completed Myogen Study AMB-220 |
Estimated Enrollment: | 60 |
Study Start Date: | April 2003 |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Study ID Numbers: | AMB-220-E |
Study First Received: | January 17, 2007 |
Last Updated: | January 17, 2007 |
ClinicalTrials.gov Identifier: | NCT00424021 |
Health Authority: | United States: Food and Drug Administration |
Idiopathic pulmonary hypertension Respiratory Tract Diseases Hypertension, Pulmonary |
Lung Diseases Vascular Diseases Hypertension |
Cardiovascular Diseases |