The purpose of this trial is to assess the tolerability and safety of NB1011 in the treatment of patients with cancers that overexpress TS, such as ovarian, gastrointestinal, colorectal, bladder, breast, and lung cancers.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
155
USC Norris Comprehensive Cancer Center
Los Angeles, California, United States
University of Minnesota
Minneapolis, Minnesota, United States
Princess Margaret Hospital
Toronto, Ontario, Canada
Safety/tolerability of NB1011 infusions
Determination of maximum tolerated dose (MTD)
Pharmacokinetics of NB1011 and its metabolite
Clinical activity as per Response Evaluation Criteria in Solid Tumors (RECIST) criteria
Assessment of TS overexpression
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