The primary purpose of this protocol is to investigate the safety and tolerability of AZD1152 when given as a continuous 2-hour infusion every week and every 2 weeks in patients with advanced solid malignancies.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
70
2-hour continuous intravenous infusion
Research Site
Amsterdam, Netherlands
Research Site
Utrecht, Netherlands
Safety and Tolerability
Time frame: Assessed at each visit
Pharmacokinetics
Time frame: Assessed at predetermined timepoints after dose administration
Effect on biomarkers
Time frame: Assessed after treatment
Anti-tumor activity
Time frame: Assessed after treatment
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