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A Study to Assess the Efficacy and Safety of Treprostinil Palmitil Inhalation Powder (TPIP) in Participants With Progressive Pulmonary Fibrosis (PPF)

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NCT07805785 · readout in 1,456 d

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

Phase
Phase 3
Status
Not yet recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
800estimated

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 2026-09-04

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2026-12-01estimatedWhen the study began enrolling
Primary completion2030-08-31estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2030-08-31estimatedThe whole study's end, after follow-up
First posted2026-09-04actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-09-04actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Progressive Pulmonary Fibrosis
  • Interstitial Lung Disease

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 From Baseline in Absolute Forced Vital Capacity (FVC) at Week 52
measured Baseline, Week 52

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