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
A study for subjects with chronic lymphocytic leukemia using study drug ABT-199
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
Additional Study Information: 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 Qualify?
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
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For more information, please contact:
Grace Lee
gl2536@cumc.columbia.edu
646-317-5205