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Completed Phase 3 Interventional Results available

Imatinib (QTI571) in Pulmonary Arterial Hypertension

ClinicalTrials.gov ID: NCT00902174

Public ClinicalTrials.gov record NCT00902174. 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 5, 2026, 8:59 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 24-week Randomized Placebo-controlled, Double-blind Multi-center Clinical Trial Evaluating the Efficacy and Safety of Oral QTI571 as an add-on Therapy in the Treatment of Severe Pulmonary Arterial Hypertension: Imatinib in Pulmonary Arterial Hypertension, a Randomized, Efficacy Study (IMPRES)

Brief summary

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

A multinational, multicenter, double blind, placebo-controlled study evaluating the efficacy and safety of imatinib as an add-on therapy in the treatment of patients with severe pulmonary arterial hypertension (PAH).

Study identification

NCT ID
NCT00902174
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
202 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
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 31, 2009
Primary completion
Apr 30, 2011
Completion
Apr 30, 2011
Last update posted
Feb 16, 2016

2009 – 2011

United States locations

U.S. sites
33
U.S. states
21
U.S. cities
28
Facility City State ZIP Site status
Novartis Investigative Site Birmingham Alabama 35294
Novartis Investigative Site Phoenix Arizona 85013
Novartis Investigative Site Los Angeles California 90024
Novartis Investigative Site San Francisco California 94143
Novartis Investigative Site Aurora Colorado 80045
Novartis Investigative Site Clearwater Florida 33756
Novartis Investigative Site Miami Beach Florida 33140
Novartis Investigative Site Weston Florida 33331
Novartis Investigative Site Atlanta Georgia 30342
Novartis Investigative Site Chicago Illinois 60637
Novartis Investigative Site Baltimore Maryland 21205
Novartis Investigative Site Boston Massachusetts 02111
Novartis Investigative Site Boston Massachusetts 02114
Novartis Investigative Site Boston Massachusetts 02118
Novartis Investigative Site Rochester Minnesota 55905
Novartis Investigative Site St Louis Missouri 63110
Novartis Investigative Site Omaha Nebraska 68131
Novartis Investigative Site Minneola New York 11501-3893
Novartis Investigative Site New York New York 10029
Novartis Investigative Site New York New York 10032
Novartis Investigative Site Durham North Carolina 27710
Novartis Investigative Site Cincinnati Ohio 45219
Novartis Investigative Site Cleveland Ohio 44106
Novartis Investigative Site Cleveland Ohio 44195
Novartis Investigative Site Oklahoma City Oklahoma 73104
Novartis Investigative Site Portland Oregon 97210
Novartis Investigative Site Philadelphia Pennsylvania 19140
Novartis Investigative Site Pittsburgh Pennsylvania 15212
Novartis Investigative Site Pittsburgh Pennsylvania 15213
Novartis Investigative Site Knoxville Tennessee 37934
Novartis Investigative Site Dallas Texas 75390
Novartis Investigative Site Houston Texas 77030
Novartis Investigative Site Milwaukee Wisconsin 53215

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 62 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00902174, 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 Feb 16, 2016 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00902174 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →