86
Participants
Start Date
April 30, 2007
Primary Completion Date
December 31, 2010
Study Completion Date
December 31, 2010
ABT-263
"Phase 1 dosing under two different schedules: 14 days on drug, 7 days off or continuous dosing.~\- 50 patients with SCLC and non-hematologic malignancies. Enrollment is closed in this arm of the study.~Phase 2a dosing under two different schedules: 14 days on drug, 7 days off or continuous dosing.~\- 40 patients with SCLC"
Site Reference ID/Investigator# 12343, Bethesda
Site Reference ID/Investigator# 4934, Charlotte
Site Reference ID/Investigator# 8324, Atlanta
Site Reference ID/Investigator# 2624, Nashville
Site Reference ID/Investigator# 2623, Chicago
Site Reference ID/Investigator# 5261, Phoenix
Site Reference ID/Investigator# 13605, Peoria
Site Reference ID/Investigator# 4718, Sacramento
Site Reference ID/Investigator# 6650, Tacoma
Site Reference ID/Investigator# 11942, Los Angeles
Site Reference ID/Investigator# 3755, Aurora
Site Reference ID/Investigator# 2625, Baltimore
Site Reference ID/Investigator# 11941, Boston
Site Reference ID/Investigator# 2626, Boston
Site Reference ID/Investigator# 7493, Edmonton
Site Reference ID/Investigator# 7635, Ottawa
Site Reference ID/Investigator# 18541, Leicester
Site Reference ID/Investigator# 2622, Manchester
Collaborators (1)
Genentech, Inc.
INDUSTRY
AbbVie (prior sponsor, Abbott)
INDUSTRY