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NCT07179380 · ClinicalTrials.gov registry record · Phase 3

Efficacy and Safety Study of Treprostinil Palmitil Inhalation Powder (TPIP) in Participants With Pulmonary Hypertension Associated With Interstitial Lung Disease (PH-ILD)

A Phase 3 study of Pulmonary Hypertension and Interstitial Lung Disease, sponsored by Insmed Incorporated.

Recruiting
Registry status
Phase 3
Development phase
344
Enrollment target
20
Study locations

NCT07179380 is a Phase 3 study of Pulmonary Hypertension and Interstitial Lung Disease that is actively recruiting participants, run by Insmed Incorporated. The registered enrollment target is 344 participants, below the 609-participant average among 72 other Pulmonary Hypertension trials with a reported enrollment target (44% lower). The trial reports 20 study locations across 12 states.

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The verdict

NCT07179380, a Phase 3 study of Pulmonary Hypertension and Interstitial Lung Disease, is actively recruiting participants, sponsored by Insmed Incorporated.

RECRUITING
Registry status
Phase 3
Development phase
344 participants
Enrollment target
20
Study locations

Study Summary

The primary objective of this study is to evaluate the effect of 24-weeks of once daily treatment with TPIP versus placebo on exercise capacity in adults with PH-ILD.

Interventions

  • DRUG Placebo
  • DRUG Treprostinil Palmitil Inhalation Powder

Study Locations (20)

Other

  • GEO002 - Tbilisi
  • GEO004 - Tbilisi
  • GEO003 - Tbilisi
  • GEO001 - Tbilisi
  • DEU010 - Gauting
  • ISR001 - Haifa
  • ISR002 - Jerusalem
  • ISR004 - Tel Aviv

Chiba

  • JPN002 - Narashino-shi
  • JPN004 - Narita

California

  • USA001 - Santa Barbara

Florida

  • USA006 - Naples

Oregon

  • USA003 - Bend

Virginia

  • USA008 - Richmond

Bavaria

  • DEU003 - München

Hesse

  • DEU005 - Immenhausen

Trial Details

FieldValue
Enrollment Target 344 participants
Start Date 2026-01-07
Est. Completion 2028-12-30
Phase Phase 3

Sponsor

Insmed Incorporated

31 total trials

What the Registry Record Tells You About NCT07179380

The ClinicalTrials.gov registry entry for NCT07179380 describes a study currently listed as recruiting, categorized as Phase 3. The registered enrollment target is 344 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 609-participant average among 72 other Pulmonary Hypertension trials with a reported enrollment target (44% lower). The listed sponsor is Insmed Incorporated, which has 31 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Pulmonary Hypertension appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT07179380 reports 20 study locations spanning 12 distinct geographic areas - top geographies include Other, Chiba, California.

Frequently Asked Questions

What is clinical trial NCT07179380 about?

NCT07179380 is a clinical study titled "Efficacy and Safety Study of Treprostinil Palmitil Inhalation Powder (TPIP) in Participants With Pulmonary Hypertension Associated With Interstitial Lung Disease (PH-ILD)". The primary objective of this study is to evaluate the effect of 24-weeks of once daily treatment with TPIP versus placebo on exercise capacity in adults with PH-ILD.

What is the current status of trial NCT07179380?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 344 participants. The study started on 2026-01-07. Estimated completion is 2028-12-30.

What conditions does trial NCT07179380 study?

This clinical trial studies the following conditions: Pulmonary Hypertension, Interstitial Lung Disease.

What interventions are being tested in trial NCT07179380?

The interventions under investigation include: Placebo (DRUG), Treprostinil Palmitil Inhalation Powder (DRUG).

Who is sponsoring clinical trial NCT07179380?

This trial is sponsored by Insmed Incorporated, which has 31 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07179380 being conducted?

This trial has 20 study locations across California, Florida, Oregon, Virginia, Bavaria. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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