Assess the Oral Bioavailability of New ABT-263 Formulations
A Single Dose Study Evaluating the Oral Bioavailability and Pharmacokinetics of the Capsule Formulation of ABT-263 in Subjects With Cancer
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Phase 1
Contacts and Locations
Study Locations
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California
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Encinitas, California, United States, 92024
- Site Reference ID/Investigator# 10281
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Santa Monica, California, United States, 90404
- Site Reference ID/Investigator# 10282
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Maryland
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Bethesda, Maryland, United States, 20892
- Site Reference ID/Investigator# 16341
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New Hampshire
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Lebanon, New Hampshire, United States, 03756
- Site Reference ID/Investigator# 9441
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New Jersey
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Hackensack, New Jersey, United States, 07601
- Site Reference ID/Investigator# 20041
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-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- > or =18 years of age;
- Non-hematologic malignancy or hematologic malignancy that is either relapsed or refractory to standard therapy, or failed up to 5 prior standard therapies or no know effective therapy exists;
- 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 1st dose of study drug;
- ECOG performance score of < or = 1;
Adequate bone marrow, renal and hepatic function per local laboratory reference range as follows:
- ANC > or = 1,000/µl;
- Platelets > or = 100,000/mm3;
- Hemoglobin > or = 9.0 g/dL;
- serum creatinine < or = 2.0 mg/dL or calculated creatinine clearance > or = 50;
- AST and ALT < or = 3.0 x ULN; Bilirubin < or = 1.5 x ULN. Gilbert's Syndrome may have a Bilirubin > 1.5 x ULN;
- aPTT, PT not to exceed 1.2 x ULN;
- Females must be surgically sterile, postmenopausal, have negative pregnancy test at screening;
Females not surgically sterile or postmenopausal & non-vasectomized males must practice at least one of the following methods of birth control:
- Total abstinence from sexual intercourse (minimum one complete menstrual cycle prior to starting study drug);
- Vasectomized partner;
- Hormonal contraceptives for at least 3 months prior to study;
- Double-barrier method (including condoms, contraceptive sponge, diaphragm or vaginal ring with spermicidal jellies or cream).
Exclusion Criteria:
- History of/clinically suspicious for cancer-related CNS disease; An allogeneic stem cell transplant.
- Underlying, predisposing condition of bleeding/currently exhibits signs of bleeding.
- History of non-chemotherapy induced thrombocytopenic associated bleeding w/i 1 year prior to the 1st dose.
- Peptic ulcer disease or other hemorrhagic esophagitis/gastritis.
- Active ITP/ history of being refractory to platelet transfusions.
- Significant history of cardiac, renal, neurologic, psychiatric, endocrinologic, metabolic, immunologic/hepatic disease.
- Females pregnant or breast-feeding.
- History of or active medical condition(s) that affects absorption or motility.
- Positive for HIV.
- Other clinically significant uncontrolled condition(s) including, but not limited to: active systemic fungal infection; neutropenic fever w/i 1 wk prior to study drug.
- Steroid therapy w/i 7 days prior to 1st dose for anti-cancer intent.
- Anti-cancer therapy including chemotherapy, immunotherapy, radiotherapy, hormonal (except hormones for hypothyroidism or ERT)/agonists required to suppress serum testosterone levels [e.g. LHRH, GnRH], any investigational therapy w/i 14 days prior to first dose of study drug.
- Biologic agent w/i 30 days prior to 1st dose.
- Anticoagulation therapy/drugs/herbal supplements affecting platelet function.
- Aspirin w/i 7 days prior to 1st dose.
- Grapefruit/grapefruit products.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: 1
|
Single dose of the current ABT-263 formulation being assessed in ongoing Phase 1/2 studies vs. a single dose of one of the new ABT-263 formulation
Single dose of the current ABT-263 formulation being assessed in ongoing Phase 1/2a studies vs. a single dose of a new ABT-263 formulation followed by QD dosing with a new ABT-263 formulation for 7 days.
|
|
Experimental: 2
|
Single dose of the current ABT-263 formulation being assessed in ongoing Phase 1/2 studies vs. a single dose of one of the new ABT-263 formulation
Single dose of the current ABT-263 formulation being assessed in ongoing Phase 1/2a studies vs. a single dose of a new ABT-263 formulation followed by QD dosing with a new ABT-263 formulation for 7 days.
|
|
Experimental: 3
|
Single dose of the current ABT-263 formulation being assessed in ongoing Phase 1/2 studies vs. a single dose of one of the new ABT-263 formulation
Single dose of the current ABT-263 formulation being assessed in ongoing Phase 1/2a studies vs. a single dose of a new ABT-263 formulation followed by QD dosing with a new ABT-263 formulation for 7 days.
|
|
Experimental: 4
|
Single dose of the current ABT-263 formulation being assessed in ongoing Phase 1/2 studies vs. a single dose of one of the new ABT-263 formulation
Single dose of the current ABT-263 formulation being assessed in ongoing Phase 1/2a studies vs. a single dose of a new ABT-263 formulation followed by QD dosing with a new ABT-263 formulation for 7 days.
|
|
Experimental: 5
|
Single dose of the current ABT-263 formulation being assessed in ongoing Phase 1/2 studies vs. a single dose of one of the new ABT-263 formulation
Single dose of the current ABT-263 formulation being assessed in ongoing Phase 1/2a studies vs. a single dose of a new ABT-263 formulation followed by QD dosing with a new ABT-263 formulation for 7 days.
|
|
Experimental: 6
|
Single dose of the current ABT-263 formulation being assessed in ongoing Phase 1/2 studies vs. a single dose of one of the new ABT-263 formulation
Single dose of the current ABT-263 formulation being assessed in ongoing Phase 1/2a studies vs. a single dose of a new ABT-263 formulation followed by QD dosing with a new ABT-263 formulation for 7 days.
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Assess the oral bioavailability of a new ABT-263 formulation relative to that of the current ABT-263 formulation being assessed in ongoing Phase 1/2a studies.
Time Frame: Two Period crossover design.
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Two Period crossover design.
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Assess the oral bioavailability of a new ABT-263 formulation relative to that of the current ABT-263 formulation being assessed in ongoing Phase 1/2a studies and assess new ABT-263 formulations after once daily dosing (QD) and twice daily dosing (BID).
Time Frame: Three Period crossover design.
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Three Period crossover design.
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Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Safety measures include number and percentage of subjects having treatment-emergent adverse events tabulated by MedDRA system organ class and preferred term, laboratory test results, lymphocyte enumeration results, vital signs, etc.
Time Frame: Two and three period crossover design
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Two and three period crossover design
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Collaborators and Investigators
Sponsor
Sponsor
Collaborators
Collaborators
Study record dates
Study Major Dates
Study Start
Study Start
Primary Completion (Actual)
Primary Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Estimate)
First Posted
Study Record Updates
Last Update Posted (Estimate)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- M10-454
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