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NCT07234032

An Open-Label Extension Study of Treprostinil Palmitil Inhalation Powder (TPIP) in Participants With Pulmonary Hypertension Associated With Interstitial Lung Disease (PH-ILD)

Not yet recruiting Phase 3 Last updated 18 November 2025
What this trial tests

Phase 3 trial testing Treprostinil Palmitil Inhalation Powder in Pulmonary Hypertension in 344 participants. Not yet recruiting.

Timeline
1 April 2026
Primary endpoint
22 January 2031
22 January 2031

Quick facts

Lead sponsorInsmed Incorporated
PhasePhase 3
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment344
Start date1 April 2026
Primary completion22 January 2031
Estimated completion22 January 2031

Drugs / interventions tested

Conditions studied

Sponsor

Insmed Incorporated — full company profile →

Who can join

18 and older, any sex, with Pulmonary Hypertension or Interstitial Lung Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary objective of this study is to evaluate the safety and tolerability of the long-term use of TPIP in participants with PH-ILD from Study INS1009-311 (NCT07179380).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Treprostinil Palmitil Inhalation Powder

Trials testing the same drug.

Other recruiting trials for Pulmonary Hypertension

Currently open trials in the same condition.

Other Insmed Incorporated trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07234032.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing