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Completed Phase 2 Interventional Results available

Ibrutinib Plus Venetoclax in Subjects With Treatment-naive Chronic Lymphocytic Leukemia /Small Lymphocytic Lymphoma (CLL/SLL)

ClinicalTrials.gov ID: NCT02910583

Public ClinicalTrials.gov record NCT02910583. 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, 2:20 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

Phase 2 Study of the Combination of Ibrutinib Plus Venetoclax in Subjects With Treatment-naïve Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma

Study identification

NCT ID
NCT02910583
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pharmacyclics LLC.
Industry
Enrollment
323 participants

Conditions and interventions

Interventions

  • Placebo Drug
  • ibrutinib Drug
  • venetoclax Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 70 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 27, 2016
Primary completion
Nov 11, 2020
Completion
Mar 26, 2024
Last update posted
Dec 19, 2024

2016 – 2024

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
14
Facility City State ZIP Site status
City of Hope /ID# 1142-0047 Duarte California 91010
Moores Cancer Center at UC San Diego /ID# 1142-0241 La Jolla California 92093
UC Irvine Medical Center - Chao Family Comprehensive Cancer Center /ID# 1142-0008 Orange California 92868-3201
Norton Cancer Center /ID# 1142-0071 Louisville Kentucky 40202
Rutgers Cancer Institute of New Jersey /ID# 1142-1193 New Brunswick New Jersey 08901
Northwell Health/Long Island Jewish Hospital /ID# 1142-0350 New Hyde Park New York 11042
New York Presbyterian Hospital/Weill Cornell Med College /ID# 1142-0200 New York New York 10021
University of Rochester Cancer Center /ID# 1142-0127 Rochester New York 14642-0001
Charlotte-Mecklenberg Hospital, Carolinas Healthcare System, Levine Cancer Inst /ID# 1142-0733 Charlotte North Carolina 28203
Cleveland Clinic Foundation /ID# 1142-0739 Cleveland Ohio 44195
University of Pennsylvania /ID# 1142-0069 Philadelphia Pennsylvania 19104
Tennessee Oncology - Chattanooga /ID# 1142-0123 Chattanooga Tennessee 37404-1108
MD Anderson Cancer Center /ID# 1142-0032 Houston Texas 77030
Swedish Cancer Institute /ID# 1142-0114 Seattle Washington 98104

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 32 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02910583, 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 19, 2024 · Synced May 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02910583 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →