Study of Weekly Motexafin Gadolinium (MGd) for Patients With Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma

Study Identifier
PCYC-0223
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact
Study Complete

Study Details

Medical Condition
  • Blood Cancer - Chronic Lymphocytic Leukemia (CLL)
  • Blood Cancer - Small Lymphocytic Lymphoma (SLL)
  • Blood Cancer - Leukemia (Other)
  • Blood Cancer - Non-Hodgkin's Lymphoma (General)
  • Study Drug
  • motexafin gadolinium
  • Phase
    Phase 1/Phase 2
    Sex
    Female & Male
    Age
    18+ years

    Protocol Summary

    The primary purpose of this study is to evaluate the safety, toxicities, dosage and response rate for an investigational drug, motexafin gadolinium, administered to patients with chronic lymphocytic leukemia or small lymphocytic lymphoma. The secondary purpose of this study is to evaluate the clinical benefit rate, the time it takes for a patient's chronic lymphocytic leukemia or small lymphocytic lymphoma to worsen, the duration of response and the time during which patients survive without chronic lymphocytic leukemia or small lymphocytic lymphoma worsening. Additionally, the patient's response to motexafin gadolinium will be compared to the response of the patient's cells in a laboratory to motexafin gadolinium.

    Study Locations

    Location
    Status
    Location
    USC Norris Cancer Hospital
    Los Angeles, California, United States, 90033
    Status
    Not applicable
    Location
    Scripps Cancer Center
    San Diego, California, United States, 92121
    Status
    Not applicable
    Location
    Northwestern University
    Chicago, Illinois, United States, 60611
    Status
    Not applicable
    Location
    The Mayo Clinic
    Rochester, Minnesota, United States, 55905
    Status
    Not applicable