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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 Sep 1, 2026, 1:43 PM 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 23, 2022
Primary completion
Mar 26, 2025
Completion
Mar 26, 2025
Last update posted
Mar 29, 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 29, 2026 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05147805 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →