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
Study Drug
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