drugset / Trial / NCT00982566
Assess the Oral Bioavailability of a New ABT-263 Formulation in Subjects With Cancer
RandomizedCrossoverOpen-labelTreatment
Summary
This is a randomized, single dose, open-label, multicenter crossover study to determine the oral bioavailability of a new ABT-263 formulation relative to that of the current ABT-263 formulation being administered in ongoing Phase 1/2a studies. Approximately 48 evaluable subjects with lymphoid malignancies, including chronic lymphocytic leukemia, and solid tumors will be enrolled in this study.
Timeline
- Start
- 2009-10
- Primary completion
- 2010-10
- Completion
- 2010-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Navitoclax | Small molecule | 200 mg | Oral |
| Subject | Navitoclax | Small molecule | 250 mg | Oral |