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Completed Phase 2 Interventional Results available

A Study Evaluating the Safety and Efficacy of Venetoclax (GDC-0199) Plus Bendamustine + Rituximab (BR) in Comparison With BR or Venetoclax Plus Rituximab in Participants With Relapsed and Refractory Follicular Non-Hodgkin's Lymphoma (fNHL)

ClinicalTrials.gov ID: NCT02187861

Public ClinicalTrials.gov record NCT02187861. 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 Jul 22, 2026, 9:45 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 II, Open-Label Study Evaluating the Safety and Efficacy of GDC-0199 (ABT-199) Plus Bendamustine Plus Rituximab (BR) in Comparison With BR Alone or GDC-0199 Plus Rituximab (R) in Patients With Relapsed and Refractory Follicular Non-Hodgkin's Lymphoma

Study identification

NCT ID
NCT02187861
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
163 participants

Conditions and interventions

Interventions

  • Venetoclax Drug
  • Bendamustine Drug
  • Rituximab Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Nov 30, 2014
Primary completion
Sep 26, 2016
Completion
Mar 15, 2018
Last update posted
Jun 4, 2019

2014 – 2018

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
Southern Cancer Center, PC Mobile Alabama 36608
Arizona Cancer Center Tucson Arizona 85719
UCLA School of Medicine; Hematology/Oncology Los Angeles California 90095
Nothwest Georgia Oncology Centers P.C Austell Georgia 30106
Northwestern University Chicago Illinois 60611
University of Illinois at Chicago College of Medicine Chicago Illinois 60612-7302
Primary Healthcare Associates SC - Harvey Harvey Illinois 60426
University of Kansas; Medical Center & Medical pavilion Westwood Kansas 66205
Sidney Kimmel Comp Cancer Ctr Baltimore Maryland 21231-1000
Hackensack University Medical Center Hackensack New Jersey 07601
James P. Wilmot Cancer Center Rochester New York 14642
University of Pennsylvania; School of Medicine Philadelphia Pennsylvania 19104
Allegheny General Hospital Pittsburgh Pennsylvania 15212
University of Pittsburgh Pittsburgh Pennsylvania 15213
University of Virginia Charlottesville Virginia 22903
VCU Massey Cancer Center Richmond Virginia 23298-003
West Virginia Uni Med. Center - Robert Byrd Health Science Morgantown West Virginia 26506

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 54 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02187861, 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 Jun 4, 2019 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02187861 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →