Pulmonary Hypertension and Imatinib

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01092897
Recruitment Status : Completed
First Posted : March 25, 2010
Last Update Posted : February 4, 2014
Information provided by (Responsible Party):
Kewal Asosingh, Ph.D, The Cleveland Clinic

March 24, 2010
March 25, 2010
February 4, 2014
March 2010
December 2012   (Final data collection date for primary outcome measure)
Measuring circulating biomarkers of imatinib affect [ Time Frame: within one year of the end of the study ]
Same as current
Complete list of historical versions of study NCT01092897 on Archive Site
Evaluate effect of imatinib on the activation of mast cells [ Time Frame: within one year of the end of the study ]
Same as current
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Pulmonary Hypertension and Imatinib
Biomarkers in Pulmonary Arterial Hypertension Treated With Imatinib
The purpose of the study is to determine whether circulating molecular and cellular biomarkers are predictive of imatinib effect on pulmonary artery hypertension.
We hypothesize that bone marrow progenitor cells are mobilized into the circulation in PAH, home to the lungs and differentiate into mast cells, which promote vascular remodeling and vasoconstriction through release of renin and chymase. As a corollary to this, we hypothesize that anti cKit tyrosine kinase inhibitor (TKI), imatinib, provides clinical benefit to patients through inhibition of mast cell progenitor proliferation, mobilization and differentiation. To test this, we will determine if mast cell progenitors and mast cell biomarkers are related to imatinib clinical response. This will be an ancillary study, part of a placebo-controlled, double-blind multi center clinical trial of imatinib in pulmonary arterial hypertension.
Observational Model: Cohort
Time Perspective: Prospective
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Probability Sample
Patients diagnosed with PAH that are enrolled in the Imatinib clinical trial.
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Subjects with PAH treated with Imatinib

*   Includes publications given by the data provider as well as publications identified by Identifier (NCT Number) in Medline.
Same as current
December 2012
December 2012   (Final data collection date for primary outcome measure)

Inclusion Criteria:

from Imatinib Trial

  • Male or Female 18 years or older
  • A current diagnosis or Pulmonary Arterial Hypertension according to the Dana Point 2008 Meeting: 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 (ASD, VSD, or PDA), or PAH associated with diet therapies or other drugs
  • A PVR> assess by RHC at screening or in the 2 months preceding the screening visit despite treatment with two or more specific PAH therapies, including endothelin receptor antagonists (ERA), phosphodiesterase 5 inhibitors (PDE5), or inhaled, intravenous or oral prostacyclin analogues for ≥3 months. On stable background therapy doses for ≥ 30 days except for warfarin (≥30 days but doses can vary even within the mouth before enrollment)
  • WHO Functional Class II-IV. For WHO Functional Class IV, one of the 2 or more specific PAH therapies must be an inhaled, intravenous or oral prostacyclin analogue, unless the subject has been shown to be intolerant of prostacyclin analogues.
  • 6MWD≥150meters and ≥450meters at screening. Distances of two consecutive 6MWTs should be within 15% of one another.
  • Ability to provide written informed consent

Exclusion Criteria: from Imatinib Trial

  • Women of childbearing potential who are not practicing birth control methods.
  • Pregnant or nursing (lactating) women, where pregnancy is defined as the state of positive hCG laboratory test (> 5 mIU/MI)
  • Have previously received treatment with imatinib
  • In treatment with chronic nitric oxide therapy
  • Pre-existing lung disease including parasitic diseases affecting lungs, congenital abnormalities of the lungs, thorax or diaphragm or bronchial asthma associated with chronic hypoxia that may contribute to severity of PAH
  • 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
  • With other diagnosis of PAH in WHO Diagnostic Group 1 re excluded including congenital systemic to pulmonary shunts (large, small that not surgically repaired, portal hypertension, HIV infection, glycogen storage disease, Gaucher's disease, hereditary hemorrhagic telangiectasia, hemoglobinopthaies, myeloproliferative disorders)
  • With a diagnosis of PAH associated with: venous hypertension (WHO Diagnostic Group II), hypoxia (WHO Diagnostic Group III), chronic pulmonary thromboembolic disease (WHO Diagnostic Group IV) or other miscellaneous causes (WHO Diagnostic Class V, which includes sarcoidosis, histiocytosis X, lympangiomatosis, compression of pulmonary vessels).
  • With deficient thrombocyte function, thrombocytopenia >50x109/L(50x103/µL)
  • With a history of acute heart failure or chronic left sided heart failure
  • With uncontrolled systemic arterial hypertension, systolic >160mmHg or diastolic >90mmHg
  • With hemoglobin <100g/L (10 g/dl)
  • With deficiencies of blood coagulation, inherited or acquired blood disorders, factor XII, factor XIII; decreased generation of coagulation factors due to acute or chronic liver diseases, efficient coagulation due to auto-antibodies against coagulation factors such as in lupus anticoagulant
  • With disseminated intravascular coagulation (DIC)
  • With evidence of major bleeding or intracranial hemorrhage
  • With a history of latent bleeding risk such as diabetic retinopathy, gastrointestinal bleeding due to gastric or duodenal ulcers, or colitis ulcerosa
  • With a history of moderate or greater hepatic insufficiency transaminase levels >4times the upper limit or normal or a bilirubin >2times the upper limit of normal
  • With a history of renal insufficiency (serum creatinine >200µmol/1or 2.6mg/dl)
  • Previous therapeutic radiation of lungs mediastinum
  • With a history of sickle cell anemia
  • With a QTcF>450msec for males and >470 msec for females at screening
  • With a history of ventricular tachycardia, ventricular fibrillation or ventricular flutter
  • Having syncope in the 3 months prior to the screening visit
  • With a history of Torsades de Pointes
  • With a history of long QT syndrome
  • Having undergone atrial septostomy in the 3 months prior to screening visit
  • Having undergone radiofrequency catheter ablation for atrial or sinus arrhythmias in the 3 months prior to screening visit
  • With an advanced, sever, or unstable disease of any type that may interfere with the primary and secondary endpoint evaluations
  • With a history of immunodeficiency diseases, including HIV
  • With a known hypersensitivity to QTI571 or drugs similar to the study drug
  • With a disability that may prevent the patient from competing all study requirements and in particular, interfere with the 6MWT assessment
  • With a life expectancy of 6months or less
  • Having used other investigational drugs at the time of enrollment, within 30 days or 5 half-lives of enrollment, whichever is longer
  • With a history of malignancy of any organ system (other than localized basal cell carcinoma of the skin), treated or untreated, within the past 5 years, regardless of whether there is evidence of local recurrence or metastases.
  • With a diagnosis of Hepatitis B or C
  • With a history of alcohol abuse within 6 months of screening
  • With a history of illicit drug abuse within 6 months of screening
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
Contact information is only displayed when the study is recruiting subjects
United States
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Kewal Asosingh, Ph.D, The Cleveland Clinic
The Cleveland Clinic
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Principal Investigator: Kewal Asosingh, M.S., Ph.D The Cleveland Clinic
The Cleveland Clinic
February 2014