CompletedPhase 1NCT04041648
Single Ascending Dose Study for Evaluation of Safety, Tolerability and Pharmacokinetics of L606
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
- Pharmosa Biopharm Inc.
- Principal Investigator
- Thomas L Hunt, MD, PhDPharmosa Biopharm Inc.PPD
- Intervention
- L606 (Liposomal Treprostinil) Inhalation Solution 51ug(drug)
- Enrollment
- 52 enrolled
- Eligibility
- 18-50 years · All sexes
- Timeline
- 2018 – 2020
Study locations (1)
- PPD, Austin, Texas, United States
Collaborators
PPD Development, LP
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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