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A Study to Evaluate the Efficacy and Safety of Once Daily Treprostinil Palmitil Inhalation Powder (TPIP) in Participants With Pulmonary Arterial Hypertension (PAH)

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NCT07481981 · readout in 862 d

Sponsored by Insmed Incorporated (industry) · INSM — their whole pipeline →.

Phase
Phase 3
Status
Recruiting
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
344estimated
Sites
3
Countries
Japan, United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2026-07-21actualWhen the study began enrolling
Primary completion2028-12-28estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2029-01-28estimatedThe whole study's end, after follow-up
First posted2026-03-19actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-19actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Pulmonary Arterial Hypertension

Interventions

  • Drug: Treprostinil Palmitil Inhalation Powder — also filed as INS1009
  • Drug: Placebo

Primary outcome

what the primary-completion date above is the date OF
Change in 6-Minute Walk Distance (6MWD) Measured at 1 to 3 Hours Post-Dose From Baseline at Week 24
measured Baseline, Week 24

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