The study will be an open label, multicenter, dose finding study. Depending on the tolerated dose up to 7 dose levels will be explored in this study, approximately 33 patients (21-54 depending on number of cohorts) may be enrolled into this study. Three patients will be initially dosed in each cohort. The primary objective of this study is to determine the recommended dose (RD) of twice daily oral doses of AZD2281 either as intermittent therapy for 7 days out of a 28-day schedule or given continuously, administered in combination with liposomal doxorubicin to patients with advanced solid tumors.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
44
capsules, oral, bd, 2 months
once every 4 weeks at 40mg/m2
Research Site
Milan, Italy
Research Site
Bellinzona, Switzerland
Research Site
Chur, Switzerland
recommended dose
Time frame: 2 months
pharmacokinetics
Time frame: 6 visits within 1 month
safety/tolerability/toxicity
Time frame: 2 months
DNA repair mechanism
Time frame: once
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.