To determine the safety, tolerability, dose-limiting toxicity (DLT), pharmacokinetic-pharmacodynamic profile, and maximum tolerated dose (MTD) of KU-0059436 when administered orally to patients with advanced solid tumours. To further evaluate the safety and efficacy of KU-0059436 in an expanded cohort of BCRA-enriched population, primarily ovarian cancer patients
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
98
Research Site
Brussels, Belgium
Research Site
Amsterdam, Netherlands
Research Site
Szczecin, Poland
Research Site
Edinburgh, United Kingdom
Research Site
London, United Kingdom
To determine the safety, tolerability, dose-limiting toxicity (DLT), and (MTD) of KU-0059436
Time frame: assessed at each visit
Objective tumour response
Time frame: assessed every 8 weeks
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