drugset / Trial / NCT05176951

A Study to Evaluate the Safety and Tolerability of Treprostinil Palmitil Inhalation Powder in Participants With Pulmonary Hypertension Associated With Interstitial Lung Disease

NCT05176951 ↗

Phase 2 Completed 39 enrolled Insmed Incorporated
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of this study is to evaluate the safety and tolerability of treprostinil palmitil inhalation powder (TPIP) compared with placebo

Timeline

Start
2022-12-22
Primary completion
2024-03-14
Completion
2024-03-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Treprostinil Palmitil Small molecule 80 ug Inhaled
Subject Treprostinil Palmitil Small molecule 640 ug Inhaled