Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 2 Interventional

A Study of ABT-263 in Combination With Dose-Intensive Rituximab, or Dose-Intensive Rituximab Alone, in Previously Untreated Patients With B-Cell, Chronic Lymphocytic Leukemia (CLL)

ClinicalTrials.gov ID: NCT01087151

Public ClinicalTrials.gov record NCT01087151. 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 Nov 9, 2026, 4:53 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase II, Multicenter, Randomized, Controlled, Open-label Study of the Safety, Efficacy and Pharmacokinetics of ABT-263 in Combination With Dose-intensive Rituximab, or Dose-intensive Rituximab Alone, in Previously Untreated Patients With B-Cell, Chronic Lymphocytic Leukemia (CLL)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This Phase II, randomized, open-label, international, multicenter trial is designed to evaluate the safety and efficacy of rituximab monotherapy when given according to a dose intense regimen and to assess the safety, efficacy, and pharmacokinetics of ABT-263 when combined with dose-intense rituximab in previously untreated patients with B-cell CLL.

Study identification

NCT ID
NCT01087151
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Genentech, Inc.
Industry
Enrollment
118 participants

Conditions and interventions

Interventions

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
Aug 2010 (Type not available)
Primary completion
Jun 2012 (Actual)
Completion
Jun 2012 (Actual)
Last update posted
Nov 2, 2016

2010 – 2012

United States locations

U.S. sites
48
U.S. states
18
U.S. cities
41
Facility City State ZIP Site status
Not listed Alhambra California 91801 —
Not listed Antioch California 94531 —
Not listed Berkeley California 94704 —
Not listed Burbank California 91505 —
Not listed Duarte California 91010 —
Not listed Dublin California 94568 —
Not listed La Jolla California 92093 —
Not listed Los Angeles California 90024 —
Not listed Los Angeles California 90073 —
Not listed Los Angeles California 90095-1772 —
Not listed Los Angeles California 90095 —
Not listed Northridge California 91325 —
Not listed Pleasant Hill California 94523 —
Not listed San Leandro California 94578-2626 —
Not listed San Luis Obispo California 93454 —
Not listed Santa Monica California 90404 —
Not listed Fort Collins Colorado 80528 —
Not listed Norwalk Connecticut 06856 —
Not listed Bay Pines Florida 33744 —
Not listed Atlanta Georgia 30322 —
Not listed Chicago Illinois 60612 —
Not listed Decatur Illinois 62526 —
Not listed Harvey Illinois 60426 —
Not listed Tinley Park Illinois 60477 —
Not listed Shreverport Louisiana 71103 —
Not listed Baltimore Maryland 21215 —
Not listed Bethesda Maryland 20817 —
Not listed Bethesda Maryland 20874 —
Not listed Randallstown Maryland 21133 —
Not listed Lansing Michigan 48909 —
Not listed Lansing Michigan 48912 —
Not listed Omaha Nebraska 68114 —
Not listed Henderson Nevada 89052 —
Not listed Las Vegas Nevada 89148 —
Not listed Las Vegas Nevada 89169 —
Not listed Reno Nevada 89502 —
Not listed Cherry Hill New Jersey 08003 —
Not listed Farmington New Mexico 87401 —
Not listed Oneida New York 13421 —
Not listed Oswego New York 13126 —
Not listed Syracuse New York 13210 —
Not listed Middletown Ohio 45042 —
Not listed Philadelphia Pennsylvania 19111 —
Not listed Pittsburgh Pennsylvania 15224 —
Not listed Corpus Christi Texas 78405 —
Not listed Lubbock Texas 79410 —
Not listed Lubbock Texas 79415 —
Not listed Everett Washington 98201 —

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 55 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01087151, 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 Nov 2, 2016 · Synced Nov 9, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01087151 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →