Imatinib (QTI571) in Pulmonary Arterial Hypertension



Status:Completed
Conditions:High Blood Pressure (Hypertension)
Therapuetic Areas:Cardiology / Vascular Diseases
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:September 2009
End Date:May 2011

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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)

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).


Key Inclusion criteria

- Male or female patients ≥18 years of age with a current diagnosis of pulmonary
arterial hypertension (PAH) according to the Dana Point 2008 Meeting: World Health
Organization (WHO) Diagnostic Group I, idiopathic or heritable (familial or sporadic)
PAH, PAH associated with collagen vascular disease including systemic sclerosis,
rheumatoid arthritis, mixed connective tissue diseases, and overlap syndrome. PAH
following one year repair of congenital heart defect [Atrial Septal Defect (ASD),
Ventricular Septal Defect (VSD) or Posterior Descending Artery (PDA)], or PAH
associated with diet therapies or other drugs

- A Pulmonary Vascular Resistance (PVR) ≥ 800 dynes.sec.cm-5 (as assessed by Right
Heart Catheterization (RHC) at screening or in the 3 months preceding the screening
visit) despite treatment with two or more specific PAH therapies, including
Endothelin Receptor Antagonists (ERAs), phosphodiesterase 5 inhibitors (PDE5), or
subcutaneous, inhaled, intravenous or oral prostacyclin analogues for ≥ 3 months.
Background therapy doses were to be stable for ≥ 30 days except for warfarin and
prostacyclin analogues ( ≥ 30 days but doses could vary even within the month before
enrollment).

- World Health Organization functional Class II-IV. For WHO Functional Class IV, one of
the 2 or more specific PAH therapies were to be an inhaled, subcutaneous, intravenous
or oral prostacyclin analogue, unless the subject showed intolerance of prostacyclin
analogues.

- 6MWD ≥ 150 meters and ≤ 450 meters at screening. Distances of two consecutive 6MWTs
were to be within 15% of one another.

Key Exclusion criteria

- With a pulmonary capillary wedge pressure > 15 mm Hg to rule out PAH secondary to
left ventricular dysfunction.

- With a diagnosis of pulmonary artery or vein stenosis

- Left ventricular ejection fraction (LVEF) < 45%

- With Disseminated Intravascular Coagulation (DIC)

- With evidence of major bleeding or intracranial hemorrhage

- With a history of elevated intracranial pressure

- With a history of latent bleeding risk such as diabetic retinopathy, gastrointestinal
bleeding due to gastric or duodenal ulcers, or colitis ulcerosa

- With a QTcF > 450 msec for males and > 470 msec for females at screening and baseline
in the absence of right bundle branch block.

- With a history of ventricular tachycardia, ventricular fibrillation or ventricular
flutter

- With a history of Torsades de Pointes

- With a history of long QT syndrome

- Having undergone atrial septostomy in the 3 months prior to the screening visit
We found this trial at
29
sites
Chicago, Illinois 60612
277
mi
from 43215
Chicago, IL
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Atlanta, Georgia 30322
432
mi
from 43215
Atlanta, GA
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Aurora, Colorado 80010
1155
mi
from 43215
Aurora, CO
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Baltimore, Maryland 21287
345
mi
from 43215
Baltimore, MD
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Birmingham, Alabama 35209
495
mi
from 43215
Birmingham, AL
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Boston, Massachusetts 02118
643
mi
from 43215
Boston, MA
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Cincinnati, Ohio 45229
95
mi
from 43215
Cincinnati, OH
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Clearwater, Florida 33756
830
mi
from 43215
Clearwater, FL
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Cleveland, Ohio 44109
123
mi
from 43215
Cleveland, OH
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Dallas, Texas 75216
914
mi
from 43215
Dallas, TX
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Durham, North Carolina 27710
352
mi
from 43215
Durham, NC
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Houston, Texas 77030
995
mi
from 43215
Houston, TX
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4451
mi
from 43215
Innsbruck,
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Knoxville, Tennessee 37934
280
mi
from 43215
Knoxville, TN
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Los Angeles, California 90095
1982
mi
from 43215
Los Angeles, CA
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Miami Beach, Florida 33140
991
mi
from 43215
Miami Beach, FL
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Milwaukee, Wisconsin 53209
335
mi
from 43215
Milwaukee, WI
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Minneola, New York 11501
496
mi
from 43215
Minneola, NY
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230 Park Avenue, 21st Floor
New York, New York 10169
1-888-669-6682)
Novartis Novartis, which was created in 1996 by the merger of the Swiss companies Ciba-Geigy...
481
mi
from 43215
New York, NY
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Oklahoma City, Oklahoma 73104
848
mi
from 43215
Oklahoma City, OK
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Omaha, Nebraska 68144
691
mi
from 43215
Omaha, NE
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Philadelphia, Pennsylvania 19102
416
mi
from 43215
Philadelphia, PA
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Phoenix, Arizona 85012
1660
mi
from 43215
Phoenix, AZ
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Pittsburgh, Pennsylvania 15224
165
mi
from 43215
Pittsburgh, PA
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Portland, Oregon 97228
Novartis Novartis, which was created in 1996 by the merger of the Swiss companies Ciba-Geigy...
2028
mi
from 43215
Portland, OR
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Rochester, Minnesota 55905
559
mi
from 43215
Rochester, MN
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San Francisco, California 94121
2111
mi
from 43215
San Francisco, CA
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St. Louis, Missouri 63110
397
mi
from 43215
St. Louis, MO
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Weston, Florida 33331
972
mi
from 43215
Weston, FL
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