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Sorafenib Study: Dosing in Patients With Pulmonary Arterial Hypertension (PAH)

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.
 
ClinicalTrials.gov Identifier: NCT00452218
Recruitment Status : Completed
First Posted : March 27, 2007
Last Update Posted : August 24, 2016
Sponsor:
Collaborator:
Bayer
Information provided by (Responsible Party):
University of Chicago

Tracking Information
First Submitted Date  ICMJE March 26, 2007
First Posted Date  ICMJE March 27, 2007
Last Update Posted Date August 24, 2016
Study Start Date  ICMJE March 2007
Actual Primary Completion Date May 2012   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: September 16, 2008)
Monthly 6MW/B [ Time Frame: 16 weeks ]
Original Primary Outcome Measures  ICMJE
 (submitted: March 26, 2007)
  • monthly 6MW/B
  • WHO functional class
  • 4 month right heart catheterization
Change History
Current Secondary Outcome Measures  ICMJE
 (submitted: September 16, 2008)
  • Efficacy [ Time Frame: 16 Weeks ]
  • World Health Organization (WHO) function class [ Time Frame: 16 weeks ]
  • Right heart catheterization [ Time Frame: 16 Week ]
  • Naughton Balke-Treadmill Test [ Time Frame: 16 Weeks ]
Original Secondary Outcome Measures  ICMJE Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title  ICMJE Sorafenib Study: Dosing in Patients With Pulmonary Arterial Hypertension (PAH)
Official Title  ICMJE Sorafenib Study: Dosing in Patients With Pulmonary Arterial Hypertension (PAH)
Brief Summary The purpose of this study is to assess the safety and tolerability of sorafenib in patients with PAH already on existing therapy with a prostacyclin [epoprostenol (Flolan)], treprostinil (Remodulin), or iloprost alone, or with or without sildenafil (Viagra/Revatio).
Detailed Description

Pulmonary arterial hypertension (PAH) is an angioproliferative vasculopathy resulting from abnormal endothelial and smooth muscle cell interactions. Idiopathic and familial PAH (formerly known as primary pulmonary hypertension) occurs more often in women than in men, with a median survival of 2.8 years if untreated and a mean age at diagnosis of 35 years. The key features of this vasculopathy causes a progressive narrowing of the pulmonary artery and their branches, resulting in right heart failure and death. Proliferating endothelial cells obliterate medium-sized precapillary arteries, thereby forming the characteristic "plexiform" lesions. When combined with the expansion of both vascular smooth muscle cells and adventitial cells in pulmonary arteries, these observations evoke comparisons to cancer pathobiology. Currently, FDA-approved therapies for PAH such as prostacyclins (epoprostenol, treprostinil, and iloprost), endothelin receptor blockers (bosentan) and phosphodiesterase inhibitors (sildenafil) all produce functional improvement (6 minute walk distance- 6MW) with minimal change in hemodynamic measurements at cardiac catheterization. Only epoprostenol has provided survival benefit with the 5-year survival, remaining at 50% without demonstrable reversal of the vasculopathy. Clearly there is a critical need for novel targets and therapies for PAH.

In this protocol, the principal investigator (PI) will leverage a large PAH referral practice with an established clinical database to assess the potential utility of kinase inhibitors as a new class of agents for protease-activated receptor (PAR). These drugs inhibit processes important to pathological blood vessel branching and growth and have been a focus for the internationally renowned University of Chicago Phase I/II trials unit in oncology led by Dr. Mark Ratain (Co-Investigator). The University of Chicago has had a major role in the drug development of the recently (12/05) FDA-approved drug, sorafenib, for advanced renal carcinoma. Sorafenib inhibits Raf-1 kinase, a regulator of endothelial apoptosis, and inhibits angiogenesis growth factor receptors VEGFR-2, PDGFR-B, and VEGFR-3.

Study Type  ICMJE Interventional
Study Phase  ICMJE Phase 1
Study Design  ICMJE Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Condition  ICMJE Pulmonary Arterial Hypertension
Intervention  ICMJE Drug: Sorafenib
200 mg daily and dose escalated to a maximum of 400 mg twice daily
Other Names:
  • BAY 43-9006
  • Nexavar
Study Arms  ICMJE Experimental: Open
Intervention: Drug: Sorafenib
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Completed
Actual Enrollment  ICMJE
 (submitted: March 26, 2007)
12
Original Enrollment  ICMJE Same as current
Actual Study Completion Date  ICMJE May 2012
Actual Primary Completion Date May 2012   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion criteria:

  • Age > 18 years
  • PAH defined as IPAH, FPAH, or PAH associated with collagen vascular disease
  • Baseline 6MW > 150 meters
  • PAH as defined by hemodynamics at diagnosis by right heart catheterization defined as: mean PAP > 25 mmHg with a normal PCWP < 15 mm Hg at rest and a PVR > 3 Wood units
  • Receiving conventional therapy as clinically indicated (oxygen, diuretics, aldosterone antagonist, calcium channel blockers, digoxin) with dose that is unchanged in the preceding 30 days prior to enrollment. This is excluding anticoagulants (warfarin) as the patient's dose may not be stable if the patient is having a cardiac catheterization at baseline within 30 days of enrollment and warfarin is being held. The dose of warfarin needs to be stable for 7 days or therapeutic with an INR = 2.0
  • If on intravenous/subcutaneous prostacyclin at a stable dose > 30 days
  • If subjects are on sildenafil, must be at a stable dose > 30 days
  • Must have right heart catheterization on prostacyclin + sildenafil within preceding 30 days. Subjects must be on a stable dose of medication within 30 days prior to cardiac catheterization and therefore there can be no dosage changes of the medications between catheterization and baseline
  • Must have pulmonary function tests (PFT) within 90 days prior to enrollment: TLC, FEV1, FVC, DLCO
  • Women of childbearing years must use adequate contraception (hormonal or barrier method of birth control) prior to enrollment. Subjects need to have a negative serum or urine pregnancy test.
  • Ability to understand and the willingness to sign a written informed consent document

Exclusion Criteria

  • PAH associated with all other etiologies: HIV, portopulmonary disease, congenital heart disease
  • Subjects with pulmonary hypertension due to thromboembolism, significant interstitial lung disease, chronic obstructive pulmonary disease, congestive heart failure, valvular heart disease
  • Subjects with (World Health Organization (WHO) functional Class IV(19)
  • Subjects with scleroderma with total lung capacity (TLC) < 60% of predicted within 30 days of screening
  • Subjects with significant obstructive lung disease with FEV1/FVC < 80% of predicted
  • Subjects with hypotension defined as systolic arterial pressure < 90 mmHg at baseline
  • Subjects with hypertension defined as systolic arterial pressure >140 mmHg at baseline or a diastolic arterial pressure > 90 mmHg
  • Subjects with impaired renal function defined as creatinine clearance < 30 ml/min as defined by the Cockcroft-Gault formula:

    • Male: creatinine clearance (ml/min) = (140-age) x (body weight in kg)/ (72x serum creatinine in mg/dl);
    • Female: creatinine clearance (ml/min)= 0.85 (140-age) x (body weight in kg)/ (72x serum creatinine in mg/dl)
  • Subjects with liver function tests (transaminases (AST/ALT), total bilirubin, and alkaline phosphatase) > 2X normal values
  • Subjects with acutely decompensated heart failure or hospitalization within the previous 30 days prior to screening
  • Subjects may not be receiving any other investigational agents
  • Subjects on endothelin receptor antagonists (bosentan, sitaxsentan, ambrisentan) or chronic arginine supplementation
  • Subjects with left ventricular ejection fraction < 45% or left ventricular shortening fraction < 0.2
  • Subjects with acute myocardial infarction within 90 days prior to screening
  • Subjects with limitations to performance of exercise measures (6MW) due to conditions other than PH associated dyspnea/fatigue
  • Subjects taking nitrates for any medical problem
  • Subjects taking phosphodiesterase inhibitors (any formulation) for erectile dysfunction
  • Subjects with a recent (< 180 days) history of pulmonary embolism verified by ventilation/perfusion scan, angiogram, or spiral CT scan
  • Pregnant or lactating women
  • Subjects with a history of current drug abuse including alcohol
Sex/Gender  ICMJE
Sexes Eligible for Study: All
Ages  ICMJE 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers  ICMJE No
Contacts  ICMJE Contact information is only displayed when the study is recruiting subjects
Listed Location Countries  ICMJE United States
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT00452218
Other Study ID Numbers  ICMJE 14636A
Has Data Monitoring Committee Yes
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement  ICMJE Not Provided
Current Responsible Party University of Chicago
Original Responsible Party Not Provided
Current Study Sponsor  ICMJE University of Chicago
Original Study Sponsor  ICMJE Same as current
Collaborators  ICMJE Bayer
Investigators  ICMJE
Principal Investigator: Mardi Gomberg, M.D. University of Chicago
PRS Account University of Chicago
Verification Date August 2016

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP