Clinical Trials Directory

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AvailableNCT06939647

An Expanded Access Study to Assess Treprostinil Palmitil Inhalation Powder (TPIP) for Participants With Pulmonary Arterial Hypertension (PAH) and Pulmonary Hypertension Associated With Interstitial Lung Disease (PH-ILD)

Treprostinil Palmitil Inhalation Powder (TPIP) in Patients With Pulmonary Arterial Hypertension or Pulmonary Hypertension Associated With Interstitial Lung Disease

Status
Available
Phase
Study type
Expanded Access
Enrollment
Sponsor
Insmed Incorporated · Industry
Sex
All
Age
18 Years
Healthy volunteers

Summary

The purpose of this study is to provide continued access to TPIP for participants who have successfully completed the open-label extension (OLE) studies of INS1009-203 for PAH or INS1009-212 for PH-ILD.

Detailed description

Participants will receive TPIP 80 micrograms (μg), 160 μg, or 320 μg, inhalation single-dose capsules, orally, once daily (QD).

Conditions

Interventions

TypeNameDescription
DRUGTreprostinil PalmitilTreprostinil Palmitil Inhalation Powder

Timeline

First posted
2025-04-23
Last updated
2026-02-27

Source: ClinicalTrials.gov record NCT06939647. Inclusion in this directory is not an endorsement.