Trials / Available
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
| Type | Name | Description |
|---|---|---|
| DRUG | Treprostinil Palmitil | Treprostinil 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.