Overview

Single Ascending Dose Study for Evaluation of Safety, Tolerability and Pharmacokinetics of L606

Status:
Completed
Trial end date:
2020-05-12
Target enrollment:
Participant gender:
Summary
The primary objective of this study is to evaluate the Pharmacokinetics, Safety and Tolerability of L606 (Liposomal Treprostinil) Inhalation Solution in Single Ascending Dose study design in healthy volunteers.
Phase:
Phase 1
Details
Lead Sponsor:
Pharmosa Biopharm Inc.
Collaborator:
PPD
Treatments:
Pharmaceutical Solutions
Treprostinil