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Completed Phase 2 Interventional Results available

A Phase 2 Open-Label Study of the Efficacy and Safety of ABT-199 (GDC-0199) in Chronic Lymphocytic Leukemia (CLL) Subjects With Relapse or Refractory to B-Cell Receptor Signaling Pathway Inhibitor Therapy

ClinicalTrials.gov ID: NCT02141282

Public ClinicalTrials.gov record NCT02141282. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 12, 2026, 12:28 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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

Study identification

NCT ID
NCT02141282
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AbbVie
Industry
Enrollment
127 participants

Conditions and interventions

Interventions

  • Venetoclax Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 99 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 9, 2014
Primary completion
Dec 21, 2021
Completion
Dec 21, 2021
Last update posted
Dec 18, 2022

2014 – 2021

United States locations

U.S. sites
15
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
Moores Cancer Center at UC San Diego /ID# 128535 La Jolla California 92093
University of California, Los Angeles /ID# 127262 Los Angeles California 90095
Stanford University School of Med /ID# 126495 Stanford California 94305-2200
Georgetown University Hospital /ID# 127261 Washington D.C. District of Columbia 20007
Emory Midtown Infectious Disease Clinic /ID# 131249 Atlanta Georgia 30322
Northwestern University Feinberg School of Medicine /ID# 126497 Chicago Illinois 60611-2927
Beth Israel Deaconess Medical Center /ID# 134509 Boston Massachusetts 02215-5400
Dana-Farber Cancer Institute /ID# 126496 Boston Massachusetts 02215
Columbia Univ Medical Center /ID# 128536 New York New York 10032-3725
New York Presbyterian Hospital Weill Cornell Medical Center /ID# 129648 New York New York 10032-3725
Univ Rochester Med Ctr /ID# 130011 Rochester New York 14642
The Ohio State University /ID# 127263 Columbus Ohio 43210
University of Pennsylvania /ID# 126860 Philadelphia Pennsylvania 19104-5502
University of Texas MD Anderson Cancer Center /ID# 126498 Houston Texas 77030
University of Utah /ID# 130813 Salt Lake City Utah 84112-5500

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02141282, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 18, 2022 · Synced May 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02141282 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →