ABT-263
Sponsors
AbbVie (prior sponsor, Abbott), AbbVie, Abbott, Genentech, Inc., Rutgers, The State University of New Jersey
Conditions
B-cell Chronic Lymphocytic LeukemiaCD20-Positive Lymphoid MalignanciesChronic Lymphocytic LeukemiaChronic Lymphoid LeukemiaFollicular LymphomaHealthy Female SubjectsHematological MalignanciesLeukemias
Phase 1
A Study of ABT-263 in Subjects With Relapsed or Refractory Lymphoid Malignancies
CompletedNCT00406809
Start: 2006-11-30End: 2016-10-31Updated: 2021-08-02
A Phase 1/2a Study of ABT-263 in Subjects With Small Cell Lung Cancer (SCLC) or Other Non-Hematological Malignancies
CompletedNCT00445198
Start: 2007-04-30End: 2010-12-31Updated: 2018-06-06
A Study of ABT-263 in Participants With Relapsed or Refractory Chronic Lymphocytic Leukemia
CompletedNCT00481091
Start: 2007-07-25End: 2022-05-12Updated: 2023-06-13
Assess the Oral Bioavailability of New ABT-263 Formulations
CompletedNCT00743028
Start: 2008-08-31Updated: 2010-10-07
Safety Study of ABT-263 in Combination With Rituximab in Lymphoid Cancers
CompletedNCT00788684
Start: 2009-07-21End: 2025-02-07Updated: 2025-02-20
Study of ABT-263 When Administered in Combination With Either Fludarabine/Cyclophosphamide/Rituximab or Bendamustine/Rituximab in Relapsed or Refractory Chronic Lymphocytic Leukemia
CompletedNCT00868413
Start: 2009-11-30End: 2013-05-31Updated: 2013-06-07
A Study Evaluating the Safety of ABT-263 in Combination With Etoposide/Cisplatin in Subjects With Cancer
CompletedNCT00878449
Start: 2009-10-31End: 2011-07-31Updated: 2018-06-06
Safety Study of ABT-263 in Combination With Gemzar (Gemcitabine) in Subjects With Solid Tumors
CompletedNCT00887757
Start: 2009-09-30End: 2011-11-30Updated: 2017-11-21
Safety Profile, MTD, and PK Profile Studies of ABT-263 When Administered in Combination With Standard and Weekly Regimens of Docetaxel in Subjects With Cancer
CompletedNCT00888108
Start: 2009-07-31End: 2012-03-31Updated: 2012-05-22
Safety Study of ABT-263 in Combination With Paclitaxel in Subjects With Solid Tumors
CompletedNCT00891605
Start: 2009-07-31End: 2012-07-31Updated: 2017-11-21
Assess the Oral Bioavailability of a New ABT-263 Formulation in Subjects With Cancer
CompletedNCT00982566
Start: 2009-10-31End: 2010-12-31Updated: 2017-11-21
A Study Evaluating ABT-263 With Erlotinib, ABT-263 With Irinotecan, and ABT-263 Monotherapy in Cancer Subjects
CompletedNCT01009073
Start: 2009-10-31End: 2013-06-30Updated: 2017-11-20
A Study to Assess the Effect of Ketoconazole on the Metabolism of ABT-263 (Navitoclax).
CompletedNCT01021358
Start: 2010-01-31Target: 12Updated: 2010-12-20
Assess the Oral Bioavailability of a New ABT-263 Formulation in Healthy Female Subjects
CompletedNCT01053520
Start: 2009-10-31End: 2010-01-31Target: 12Updated: 2010-11-09
Phase 2
Study Assessing the Safety and Efficacy of ABT-263 in Subjects With B-cell Chronic Lymphocytic Leukemia (CLL) Who Have Failed at Least One Prior Fludarabine-containing Regimen
WithdrawnNCT00918450
Start: 2010-03-31Target: 150Updated: 2010-02-26
A Study of ABT-263 in Combination With Dose-Intensive Rituximab, or Dose-Intensive Rituximab Alone, in Previously Untreated Patients With B-Cell, Chronic Lymphocytic Leukemia (CLL)
CompletedNCT01087151
Start: 2010-08-31End: 2012-06-30Updated: 2016-11-02
Navitoclax and Abiraterone Acetate With or Without Hydroxychloroquine in Treating Patients With Progressive Metastatic Castrate Refractory Prostate Cancer
TerminatedNCT01828476
Start: 2013-06-30End: 2016-03-03Updated: 2017-05-04
A Study of ABT-263 as Single Agent in Women With Platinum Resistant/Refractory Recurrent Ovarian Cancer
CompletedNCT02591095
Start: 2016-01-31End: 2019-03-31Updated: 2019-03-19