The purpose of this study is to evaluate safety and efficacy ofKarenitecin (BNP1350) as a treatment of adults with brain tumors.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
40
Karenitecin 1.0 mg/m2 administered as a single 60-minute IV infusion daily for five consecutive days. The cycle is repeated every 21 days until occurrence of progressive disease or unacceptable toxicity.
For Information call 210-614-1701 for a site near you
Durham, North Carolina, United States
Objective Tumor Response Rate
Time frame: Randomization to end of treatment
Overall Survival
Time frame: Randomization to date of death due to any cause
Overall Safety
Time frame: Randomization to end of study participation
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