This is a phase 1, open-label, dose-escalation clinical trial to evaluate the safety of SGN-75 in patients with CD70-positive relapsed or refractory non-Hodgkin lymphoma or metastatic renal cell carcinoma.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
58
SGN-75 (IV) in 21- or 28-day cycles; dose range: 0.3-9 mg/kg
University of Alabama at Birmingham
Birmingham, Alabama, United States
City of Hope National Medical Center
Duarte, California, United States
UCLA Medical Center / University of California at Los Angeles
Los Angeles, California, United States
Incidence of adverse events and laboratory abnormalities
Time frame: Through 1 month following last dose
Best clinical response
Time frame: Every 2 months
Duration of response, progression-free survival
Time frame: Every 3 months until progression of disease or initiation of new treatment for cancer
Blood concentrations of SGN-75 and metabolites
Time frame: Through 1 month following last dose
Incidence of antitherapeutic antibodies
Time frame: Through 1 month following last dose
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Karmanos Cancer Institute / Wayne State University
Detroit, Michigan, United States
Mayo Clinic
Rochester, Minnesota, United States
Memorial Sloan Kettering Cancer Center
New York, New York, United States
Sarah Cannon Research Institute
Nashville, Tennessee, United States
MD Anderson Cancer Center / University of Texas
Houston, Texas, United States
Seattle Cancer Care Alliance / University of Washington
Seattle, Washington, United States