CompletedPhase 1NCT01153386
Pharmacokinetic Linearity and Comparative Bioavailability of Treprostinil Diethanolamine
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
- United Therapeutics
- Principal Investigator
- Thomas L Hunt, MD, PhDPPD Development, LP
- Intervention
- Treprostinil diethanolamine(drug)
- Enrollment
- 36 enrolled
- Eligibility
- 18-55 years · All sexes
- Timeline
- 2010 – 2010
Study locations (1)
- PPD Development, Austin, Texas, United States
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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