Assess the Oral Bioavailability of New ABT-263 Formulations

PHASE1CompletedINTERVENTIONAL
Enrollment

36

Participants

Timeline

Start Date

August 31, 2008

Primary Completion Date

August 31, 2010

Conditions
Chronic Lymphocytic LeukemiaLymphomasLeukemias
Interventions
DRUG

ABT-263

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

DRUG

ABT-263

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.

DRUG

ABT-263

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.

Trial Locations (5)

20892

Site Reference ID/Investigator# 16341, Bethesda

90404

Site Reference ID/Investigator# 10282, Santa Monica

92024

Site Reference ID/Investigator# 10281, Encinitas

03756

Site Reference ID/Investigator# 9441, Lebanon

07601

Site Reference ID/Investigator# 20041, Hackensack

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Genentech, Inc.

INDUSTRY

lead

Abbott

INDUSTRY