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Terminated Phase 2 Interventional

Lumiliximab With Fludarabine, Cyclophosphamide, and Rituximab (FCR) Versus FCR Alone in Subjects With Relapsed Chronic Lymphocytic Leukemia (CLL)

ClinicalTrials.gov ID: NCT00391066

Public ClinicalTrials.gov record NCT00391066. 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 Apr 29, 2026, 5:14 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 Randomized, Open Label, Multicenter, Phase 2 Study to Evaluate the Safety and Efficacy of Lumiliximab in Combination With Fludarabine, Cyclophosphamide, and Rituximab Versus Fludarabine, Cyclophosphamide, and Rituximab Alone in Subjects With Relapsed Chronic Lymphocytic Leukemia

Study identification

NCT ID
NCT00391066
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Biogen
Industry
Enrollment
627 participants

Conditions and interventions

Interventions

  • FCR Drug
  • FCR + Lumiliximab 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
Oct 31, 2006
Primary completion
Jun 30, 2010
Completion
Nov 30, 2010
Last update posted
Oct 1, 2015

2006 – 2010

United States locations

U.S. sites
53
U.S. states
23
U.S. cities
53
Facility City State ZIP Site status
Research Site Scottsdale Arizona
Research Site Alhambra California
Research Site Burbank California
Research Site Fullerton California
Research Site La Jolla California
Research Site Long Beach California
Research Site Los Angeles California
Research Site Northridge California
Research Site Oxnard California
Research Site Pomona California
Research Site Redondo Beach California
Research Site Sacramento California
Research Site Santa Maria California
Research Site Fort Myers Florida
Research Site Atlanta Georgia
Research Site Marietta Georgia
Research Site Chicago Illinois
Research Site Maywood Illinois
Research Site Indianapolis Indiana
Research Site Overland Park Kansas
Research Site Shreveport Louisiana
Research Site Boston Massachusetts
Research Site Detroit Michigan
Research Site Saint Joseph Michigan
Research Site Ypsilant, Michigan
Research Site Minneapolis Minnesota
Research Site Columbia Missouri
Research Site St Louis Missouri
Research Site Billings Montana
Research Site Omaha Nebraska
Research Site Hackensack New Jersey
Research Site Morristown New Jersey
Research Site Chapel Hill North Carolina
Research Site Raleigh North Carolina
Research Site Columbus Ohio
Research Site Kettering Ohio
Research Site Philadelphia Pennsylvania
Research Site Pittsburgh Pennsylvania
Research Site Greenville South Carolina
Research Site Nashville Tennessee
Research Site Austin Texas
Research Site Bedford Texas
Research Site Dallas Texas
Research Site Fort Worth Texas
Research Site Fredericksburg Texas
Research Site Houston Texas
Research Site San Antonio Texas
Research Site Norfolk Virginia
Research Site Roanoke Virginia
Research Site Kennewick Washington
Research Site Saint Louis Washington
Research Site Spokane Washington
Research Site Yakima Washington

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 141 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00391066, 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 Oct 1, 2015 · Synced Apr 29, 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 protocol, eligibility criteria, and contact information for NCT00391066 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →