Trial record 1 of 1 for:    Zileuton With or Without Celecoxib As Chemopreventive Agents in Smokers
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Zileuton With or Without Celecoxib As Chemopreventive Agents in Smokers

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
National Cancer Institute (NCI)
ClinicalTrials.gov Identifier:
NCT01021215
First received: November 24, 2009
Last updated: October 7, 2013
Last verified: October 2013

November 24, 2009
October 7, 2013
May 2010
September 2011   (final data collection date for primary outcome measure)
Change in urinary LTE4 and PGE-M levels [ Time Frame: Baseline and day 6 ] [ Designated as safety issue: No ]
Pre- and post- treatment differences in biomarker values measured in each treatment arm will be compared using the paired t-test should the data conform to the normality assumption or one-sample Wilcoxon rank-sum test.
Pre- and Post-treatment differences of Urinary LTE4 and PGE-M Levels [ Time Frame: Baseline and at final clinic visit Day 7 ] [ Designated as safety issue: No ]
Complete list of historical versions of study NCT01021215 on ClinicalTrials.gov Archive Site
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Zileuton With or Without Celecoxib As Chemopreventive Agents in Smokers
Modulation of Arachidonic Acid Metabolism by Chemopreventive Agents in Smokers

The goal of this clinical research study is to learn how zileuton alone or the combination of zileuton and celecoxib may affect certain chemicals in the body that may be linked with a risk for smoking-related lung disease. These effects will be measured by a urine test

PRIMARY OBJECTIVES:

I. To determine whether short-term administration of zileuton, a 5-lipoxygenase (5-LO) inhibitor, in current smokers will suppress the formation of urinary leukotriene E4 (LTE4) and shunt arachidonic acid into the cyclooxygenase (COX) pathway, resulting in elevated urinary prostaglandin E-metabolite (PGE-M).

SECONDARY OBJECTIVES:

I. To determine whether short-term co-administration of celecoxib, a selective COX-2 inhibitor, and zileuton suppresses levels of both urinary LTE4 and PGE-M in current smokers.

II. To evaluate the association between baseline levels of urinary LTE4 and magnitude of the arachidonic acid shunt induced by zileuton.

OUTLINE: Patients are randomized to 1 of 2 treatment arms.

ARM I: Patients receive zileuton orally (PO) twice daily (BID) on days 1-6.

ARM II: Patients receive zileuton as in Arm I and celecoxib PO BID on days 1-6.

Interventional
Phase 1
Phase 2
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Prevention
Tobacco Use Disorder
  • Drug: zileuton
    Given PO
  • Drug: celecoxib
    Given PO
  • Other: laboratory biomarker analysis
    Correlative studies
  • Experimental: Arm I (zileuton)
    Patients receive zileuton PO BID on days 1-6.
    Interventions:
    • Drug: zileuton
    • Other: laboratory biomarker analysis
  • Experimental: Arm II (zileuton and celecoxib)
    Patients receive zileuton as in Arm I and celecoxib PO BID on days 1-6.
    Interventions:
    • Drug: zileuton
    • Drug: celecoxib
    • Other: laboratory biomarker analysis
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
80
Not Provided
September 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Male or female current tobacco smokers with more or equal to 10 pack years of self-reported smoking exposure and an average of more or equal to 10 cigarettes/day
  • ECOG performance status 0 or 1 (Karnofsky 70-100%)
  • Total bilirubin less or equal to 2 X ULN
  • Direct bilirubin less or equal to 2 X ULN
  • AST (SGOT) less or equal to 2 X ULN
  • ALT (SGPT) less or equal to 2 X ULN
  • Alkaline phosphatase less or equal to 2 X ULN
  • If the participant is female, of childbearing potential and not lactating, she has a documented negative serum pregnancy test within 14 days prior to randomization

Exclusion Criteria:

  • The participant has active cancer (excluding non-melanoma skin cancer)
  • The participant has a history of curatively treated cancer with surgical therapy finished within 6 months prior to the Screening visit; or has had chemotherapy, cancer-related immunotherapy, hormonal therapy (other than HRT for menopause), or radiation therapy within 12 months of the screening visit
  • The participant has a chronic inflammatory condition, including but not limited to, ulcerative colitis, Crohn's disease, rheumatoid arthritis, psoriasis, gout and pancreatitis
  • The participant has an ongoing or active infection, including but not limited to HIV, pneumonia, urinary tract infection
  • The participant has a history of NSAID use, including aspirin (low-dose aspirin also prohibited) and selective COX-2 inhibitors within the previous 4 weeks
  • The participant has used zileuton or a leukotriene receptor antagonist within the previous 4 weeks
  • The participant has a history of corticosteroid use (excluding topical nasal sprays and dermal application) within the last 6 weeks
  • The participant has an acute or chronic kidney disorder
  • The participant exhibits clinical evidence of active liver disease or history of chronic liver disease
  • The participant has active cardiac disease, or a history of myocardial infarction, angina or coronary artery disease within the past 6 months
  • The participant has a history of a cerebrovascular accident (CVA) or transient ischemic attack (TIA)
  • The participant has a bleeding history
  • The participant is taking drugs known to interact with zileuton or celecoxib, including theophylline, warfarin, propranolol, fluconazole or lithium
  • The participant has received any investigational medication within 30 days of the screening visit or is scheduled to receive an investigational agent during the study
  • The participant is pregnant or nursing; women must not be pregnant or lactating
  • The participant is a female of child-bearing potential (women are considered not of childbearing potential if they are at least two years postmenopausal and/or surgically sterile) who has not used adequate contraception (abstinence; barrier methods such as IUD, diaphragm with spermicidal gel, condom, or others; and hormonal methods such as birth control pills or others) since her last menses prior to study entry
  • The participant is a female of child-bearing potential or male who does not agree to use adequate contraception for the duration of study participation; should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her study physician immediately
  • The participant has participated in the study previously and was withdrawn
  • Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
  • Pregnant or nursing participants or those who are HIV-positive will be excluded from the study
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01021215
NCI-2013-00730, NCI-2013-00730, 2009-0804, 2009-0804, N01CN35159
Not Provided
National Cancer Institute (NCI)
National Cancer Institute (NCI)
Not Provided
Principal Investigator: Powel Brown M.D. Anderson Cancer Center
National Cancer Institute (NCI)
October 2013

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