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A Study to Assess the Effect of Rifampin on the Metabolism of Navitoclax

This study has been completed.
Sponsor:
Information provided by:
Abbott
ClinicalTrials.gov Identifier:
NCT01121133
First received: May 10, 2010
Last updated: June 4, 2011
Last verified: May 2011

May 10, 2010
June 4, 2011
May 2010
May 2011   (final data collection date for primary outcome measure)
To determine the effect of rifampin on the pharmacokinetics of navitoclax. [ Time Frame: Weekly ] [ Designated as safety issue: Yes ]
Same as current
Complete list of historical versions of study NCT01121133 on ClinicalTrials.gov Archive Site
To determine the safety of navitoclax when administered alone and in combination with rifampin in these patients. [ Time Frame: Daily ] [ Designated as safety issue: Yes ]
Same as current
Not Provided
Not Provided
 
A Study to Assess the Effect of Rifampin on the Metabolism of Navitoclax
A Phase I Study to Assess the Effect of a CYP3A Inducer (Rifampin) on the Pharmacokinetics of ABT-263 (Navitoclax)

This is an open-label, single or multiple center study to determine the interaction of rifampin with navitoclax (ABT-263) in approximately 12 subjects with cancer.

Not Provided
Interventional
Phase 1
Allocation: Non-Randomized
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Lymphoma, Including Chronic Lymphocytic Leukemia
  • Solid Tumors
  • Drug: navitoclax
    Subjects will be dosed with Navitoclax, then dosed with Navitoclax in combination with Rifampin.
    Other Name: ABT-263, navitoclax
  • Drug: Rifampin
    Subjects will be dosed with Navitoclax, then, dosed with Navitoclax in combination with Rifampin.
    Other Name: rifampin
Experimental: Arm A (navitoclax and rifampin)
Interventions:
  • Drug: navitoclax
  • Drug: Rifampin
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
12
May 2011
May 2011   (final data collection date for primary outcome measure)

Inclusion Criteria

  • 18 years of age or older.
  • Has a non-hematologic malignancy (radiographic, histologic, or cytologic confirmation), or hematologic malignancy (histologic or cytologic confirmation) that is either: relapsed or refractory to standard therapy, failed at least one prior therapy or no known effective therapy exists.
  • In the investigator's opinion, the subject's life expectancy is at least 90 days.
  • If clinically indicated, (e.g., subjects over the age of 70) subjects must have documented brain imaging (MRI or CT) negative for subdural or epidural hematoma within 28 days prior to the first dose of study drug.

Exclusion Criteria

  • Subjects with brain metastases must have clinically controlled neurologic symptoms, defined as surgical excision and/or radiation therapy followed by 21 days of stable neurologic function and no evidence of CNS disease progression as determined by CT or MRI within 21 days prior to the first dose of study drug.
  • History of or is clinically suspicious for cancer-related central nervous system (CNS) disease.
  • Has undergone an allogeneic stem cell transplant.
  • Has an underlying, predisposing condition of bleeding or currently exhibits signs of bleeding.
  • Has active peptic ulcer disease or other hemorrhagic esophagitis/gastritis.
  • Has active immune thrombocytopenic purpura or a history of being refractory to platelet transfusions (within 1 year prior to the first dose of study drug).
  • Significant history of cardiovascular disease (e.g., MI, thrombotic or thromboembolic event in the last 6 months), renal, neurologic, psychiatric, endocrinologic, metabolic, immunologic, or hepatic disease. Female subject is pregnant or breast-feeding.
  • History of or an active medical condition(s) that affects absorption or motility (e.g., Crohn's disease, celiac disease, gastroparesis, short bowel syndrome, etc).
  • Subject exhibits evidence of other clinically significant uncontrolled condition(s) including, but not limited to:

    • tuberculosis
    • diagnosis of fever and neutropenia within 1 week prior to study drug administration
  • Received any anti-cancer therapy including chemotherapy, immunotherapy, radiotherapy, hormonal (with the exception of hormones for hypothyroidism or estrogen replacement therapy [ERT], or agonists required to suppress serum testosterone levels [e.g., LHRH, GnRH, etc.] for subjects with prostate cancer Subject is currently receiving or requires anticoagulation therapy (e.g., warfarin at any dose) or any drugs or herbal supplements that affect platelet function, with the exception of low-dose heparin used to maintain the patency of a catheter.
  • Subject has used known inhibitors (e.g., ketoconazole) or inducers (e.g., rifampin and carbamazepine) of cytochrome P450 3A (CYP3A) within 1 week prior to first dose of study.
  • Subject has a history of hypersensitivity to any of the rifamycins.
  • In the opinion of the Investigator, the subject is an unsuitable candidate to receive ABT-263.
  • History of or is clinically suspicious for cancer-related central nervous system (CNS) disease.
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01121133
M10-955
No
Kyle Holen, M.D./Medical Director, Abbott
Abbott
Not Provided
Not Provided
Abbott
May 2011

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