drugset / Trial / NCT00982566

Assess the Oral Bioavailability of a New ABT-263 Formulation in Subjects With Cancer

NCT00982566

Phase 1 Completed 37 enrolled AbbVie Genentech, Inc. · collab
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

EvaluationDrugModalityDoseRoute
Subject Navitoclax Small molecule 200 mg Oral
Subject Navitoclax Small molecule 250 mg Oral