TerminatedPhase 2NCT01725269
Long-term Study of AIR001 in Subjects With WHO Group 1 Pulmonary Arterial Hypertension Who Completed AIR001-CS05
Studying Drug- or toxin-induced pulmonary arterial hypertension
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Aires Pharmaceuticals, Inc.
- Principal Investigator
- Adaani E Frost, M.D., MDBaylor College of Medicine, Houston
- Intervention
- AIR001(drug)
- Enrollment
- 17 enrolled
- Eligibility
- 18-75 years · All sexes
- Timeline
- 2013 – 2014
Study locations (25)
- UCSD Medical Center, La Jolla, California, United States
- UCLA Medical Center, Torrance, California, United States
- University of Colorado Denver, Aurora, Colorado, United States
- Kentuckiana Pulmonary Associates, Louisville, Kentucky, United States
- University of Maryland Medical Center, Baltimore, Maryland, United States
- Tufts Medical Center, Boston, Massachusetts, United States
- Brigham and Women's Hospital, Boston, Massachusetts, United States
- Boston University School of Medicine, Boston, Massachusetts, United States
- Washington University School of Medicine, St Louis, Missouri, United States
- Duke University Medical Center, Durham, North Carolina, United States
- University of Cincinnati, Cincinnati, Ohio, United States
- The Ohio State University Medical Center, Columbus, Ohio, United States
- University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States
- University of Texas Southwestern Medical Center, Dallas, Texas, United States
- Adaani Frost, M.D., Houston, Texas, United States
- +10 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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