Evaluation of Safety and Efficacy of Fludarabine, Cyclophosphamide, and Rituximab (FCR) +/- Lumiliximab in Subjects With Previously Untreated Chronic Lymphocytic Leukemia (CLL)

PHASE2TerminatedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

February 29, 2008

Primary Completion Date

June 30, 2010

Study Completion Date

September 30, 2010

Conditions
Chronic Lymphocytic Leukemia
Interventions
DRUG

Lumiliximab + FCR

Dose, schedule, and duration in the protocol

DRUG

FCR

Dosage, schedule, and duration in the protocol

Trial Locations (36)

1000

Research Site, Brussels

1090

Research Site, Vienna

1190

Research Site, Vienna

1200

Research Site, Brussels

2060

Research Site, Antwerp

2145

Research Site, Westmead

2610

Research Site, Wilrijk

3000

Research Site, Leuven

3058

Research Site, Melbourne (Coburg)

5530

Research Site, Mont-Godinne

7601

Research Site, Hackensack

8036

Research Site, Graz

8800

Research Site, Roeselare

32610

University of Florida/Pulmonary, Critical Care & Sleep Medicine, Gainesville

33136

University of Miami Miller School of Medicine, Miami

33604

Research Site, Pessac

34295

Research Site, Montpellier

37044

Research Site, Tours

37232

Vanderbilt University Medical Center-IPF Program, Nashville

48202

Research Site, Detroit

59000

Research Site, Lille

60612

Research Site, Chicago

60637

University of Chicago, Chicago

67000

Research Site, Strasbourg

69495

Research Site, Pierre-Bénite

75475

Research Site, Paris

98101

Research Site, Seattle

03756

Dartmouth-Hitchcock Medical Center, Lebanon

K1H1A2

Research Site, Ottawa

15-276

Research Site, Bialystok

80-952

Research Site, Gdansk

93-510

Research Site, Lodz

EX25DW

Research Site, Exeter

PL68DH

Research Site, Plymouth

WC1E6DB

Research Site, London

BA13NG

Research Site, Bath, Avon

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Biogen

INDUSTRY