Trial Information
A Dose-Finding Study of CpG 7909 in Previously Treated Chronic Lymphocytic Leukemia
Inclusion Criteria:
- Diagnosis of CLL
- CLL previously treated
- Hemoglobin >/= 10
- Platelets >/= 50,000
- Neutrophils >= 1,000 -
Exclusion Criteria:
- patients with brain mets
- patients with autoimmune disease
- patients on corticosteroids or immunosuppressants
- patients with uncontrolled intercurrent illness
- pregnant women
- HIV patients receiving combination anti-retroviral therapy
Type of Study:
Interventional
Study Design:
Allocation: Randomized, Endpoint Classification: Bio-availability Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Principal Investigator
Brian Link, MD
Investigator Role:
Principal Investigator
Investigator Affiliation:
UIHC
Authority:
United States: Food and Drug Administration
Study ID:
200402002
NCT ID:
NCT00233506
Start Date:
July 2004
Completion Date:
Related Keywords:
- Chronic Lymphocytic Leukemia
- CpG 7909
- CLL
- Leukemia
- Leukemia, Lymphocytic, Chronic, B-Cell
- Leukemia, Lymphoid
Name | Location |
University of Iowa |
Iowa City, Iowa 52242 |
Mayo Clinic |
Rochester, Minnesota 55905 |