This study will examine the safety profile of SGN-CD70A. The study will test increasing doses of SGN-CD70A given every 3 weeks (or an alternate dosing schedule up to every 6 weeks) to small groups of patients. The goal is to find the highest dose of SGN-CD70A that can be given to patients without causing unacceptable side effects. The pharmacokinetics and antitumor activity of SGN-CD70A will also be evaluated.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
38
Given intravenously every 3 weeks (or an alternate dosing schedule up to every 6 weeks)
University of Alabama at Birmingham
Birmingham, Alabama, United States
Incidence of adverse events
Time frame: Through 1 month following last dose
Incidence of laboratory abnormalities
Time frame: Through 1 month following last dose
Blood concentrations of SGN-CD70A and metabolites
Time frame: Through 3 to 6 weeks after dosing
Incidence of antitherapeutic antibodies
Time frame: Through 1 month following last dose
Objective response rate
Time frame: Through 1 month following last dose
Progression-free survival
Time frame: Approximately 3 years
Duration of response
Time frame: Approximately 3 years
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