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Completed Phase 2 Interventional

A Study to Evaluate the Efficacy, Safety and Pharmacokinetics of Treprostinil Palmitil Inhalation Powder in Participants With Pulmonary Arterial Hypertension

ClinicalTrials.gov ID: NCT05147805

Public ClinicalTrials.gov record NCT05147805. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 17, 2026, 3:20 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2b, Randomized, Double-Blind, Multicenter, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Treprostinil Palmitil Inhalation Powder in Participants With Pulmonary Arterial Hypertension

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The main objective of the study is to assess the effect of treprostinil palmitil inhalation powder (TPIP) compared with placebo on pulmonary vascular resistance.

Study identification

NCT ID
NCT05147805
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Insmed Incorporated
Industry
Enrollment
102 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 24, 2022 (Actual)
Primary completion
Mar 27, 2025 (Actual)
Completion
Mar 27, 2025 (Actual)
Last update posted
Mar 30, 2026

2022 – 2025

United States locations

U.S. sites
21
U.S. states
10
U.S. cities
19
Facility City State ZIP Site status
USA025 Phoenix Arizona 85006 —
USA022 Scottsdale Arizona 85258 —
USA021 Tucson Arizona 85724 —
USA023 Sacramento California 95817 —
USA002 West Hollywood California 90048 —
USA008 Gainesville Florida 32610 —
USA005 Jacksonville Florida 32224 —
USA007 Orlando Florida 32803 —
USA011 Tampa Florida 33601 —
USA010 Winter Park Florida 32792-3800 —
USA009 Atlanta Georgia 30309 —
USA006 Chicago Illinois 60611 —
USA001 Chicago Illinois 60612 —
USA013 Indianapolis Indiana 46260 —
USA014 Iowa City Iowa 52242 —
USA003 Kansas City Kansas 66160 —
USA102 New York New York 10021 —
USA017 New York New York 10032-1559 —
USA016 Dallas Texas 75246 —
USA012 Denison Texas 75020 —
USA018 Houston Texas 77030 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 71 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05147805, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 30, 2026 · Synced Oct 17, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05147805 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →