A Phase 2 Open-Label Study of the Efficacy and Safety of ABT-199 (GDC-0199) in Chronic Lymphocytic Leukemia Subjects with Relapse or Refractory to B-cell Receptor Signaling Pathway Inhibitor Therapy
Sponsor: |
AbbVie |
Enrolling: |
Male and Female Patients |
IRB Number: |
AAAN9606 |
U.S. Govt. ID: |
NCT02141282 |
Contact: |
Grace Lee: 646-317-5205 / gl2536@cumc.columbia.edu |
The purpose of this study is to evaluate how well the study drug ABT-199 works and safety of ABT-199 in subjects with Chronic Lymphocytic Leukemia (CLL) whose cancer has come back (relapsed) after treatment or no response (refractory) to treatment with B-cell receptor signaling pathway inhibitor therapy, namely Ibrutinib and/or Idelalisib. In addition, substances found in the blood, bone marrow and tissue (biomarkers) that may indicate the effects or progress of the leukemia and the activity of ABT-199 will be studied.
This study is closed
Investigator
Nicole Lamanna, MD
Do you have refractory or relapsed Chronic Lymphocytic Leukemia (CLL)? |
Yes |
No |
Do you have a confirmed diagnosis of Chronic Lymphocytic Leukemia (CLL)? |
Yes |
No |