Escalating Dose Study in Subjects With Relapsed or Refractory B Cell Non-Hodgkin Lymphoma, Chronic Lymphocytic Leukemia, and Waldenstrom's Macroglobulinemia

PHASE1CompletedINTERVENTIONAL
Enrollment

113

Participants

Timeline

Start Date

July 18, 2011

Primary Completion Date

June 26, 2015

Study Completion Date

June 26, 2015

Conditions
B Cell Non-Hodgkin's LymphomaChronic Lymphocytic LeukemiaWaldenstrom Macroglobulinemia
Interventions
DRUG

AVL-292

125 mg to 625 mg orally, once a day, for 28 days (28 days equals 1 cycle). Number of cycles: until progression or unacceptable toxicity develops

Trial Locations (13)

10029

Mount Sinai School of Medicine and Mount Sinai Graduate School of Biological Sciences, New York

14642

University of Rochester Medical Center, Rochester

32224

Mayo Clinic Jacksonville, Jacksonville

35805

Clearview Cancer Institute Oncology Specialties, P.C, Huntsville

44195

Cleveland Clinic, Cleveland

47905

Horizon Oncology Center, Lafayette

60611

Northwestern University, Chicago

77030

The University of Texas MD Anderson Cancer Center, Houston

77380

US Oncology, The Woodlands

78229

University of Texas Health Sciences Center, San Antonio

85719

University of Arizona SPORE, Tucson

92093-0960

University of California San Diego, La Jolla

02115

Dana Farber Cancer Institute, Boston

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

The Leukemia and Lymphoma Society

OTHER

lead

Celgene

INDUSTRY