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Terminated Phase 3 Interventional Results available

Extension to QTI571A2301 to Evaluate the Long-term Safety, Tolerability and Efficacy of Imatinib in Severe Pulmonary Arterial Hypertension (PAH)

ClinicalTrials.gov ID: NCT01117987

Public ClinicalTrials.gov record NCT01117987. 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 26, 2026, 9:11 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

An Extension to QTI571A2301 to Evaluate the Long-term Safety, Tolerability and Efficacy of Oral QTI571 (Imatinib) in the Treatment of Severe Pulmonary Arterial Hypertension: IMPRES Extension

Brief summary

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

This is a multinational, multi center extension study. This study will provide data on the long-term safety, tolerability, and efficacy of imatinib in the treatment of severe pulmonary arterial hypertension.

Study identification

NCT ID
NCT01117987
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
144 participants

Conditions and interventions

Interventions

Drug

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
Apr 2010 (Type not available)
Primary completion
Apr 2014 (Actual)
Completion
Apr 2014 (Actual)
Last update posted
Aug 13, 2015

2010 – 2014

United States locations

U.S. sites
19
U.S. states
16
U.S. cities
19
Facility City State ZIP Site status
Novartis Investigative Site Birmingham Alabama 35294-0006 —
Novartis Investigative Site Phoenix Arizona 85013 —
Novartis Investigative Site Los Angeles California 90095 —
Novartis Investigative Site San Francisco California 94143 —
Novartis Investigative Site Weston Florida 33331 —
Novartis Investigative Site Chicago Illinois 60637 —
Novartis Investigative Site Rochester Minnesota 55905 —
Novartis Investigative Site St Louis Missouri 63110 —
Novartis Investigative Site Omaha Nebraska 68131 —
Novartis Investigative Site Mineola New York 11501 —
Novartis Investigative Site New York New York 10029 —
Novartis Investigative Site Durham North Carolina 27710 —
Novartis Investigative Site Cincinnati Ohio 45219 —
Novartis Investigative Site Cleveland Ohio 44195 —
Novartis Investigative Site Oklahoma City Oklahoma 73104 —
Novartis Investigative Site Tualatin Oregon 97062 —
Novartis Investigative Site Pittsburgh Pennsylvania 15213 —
Novartis Investigative Site Houston Texas 77030 —
Novartis Investigative Site Milwaulkee 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 40 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01117987, 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 Aug 13, 2015 · Synced Oct 26, 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 NCT01117987 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →