The purpose of this study is to assess safety and tolerability of multiple ascending doses of AZD1152 and to assess effect of AZD1152 on the rate of complete remission in patients with relapsed acute myeloid leukaemia who are not considered to be suitable for standard chemotherapy.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
30
intravenous
Research Site
Nagoya, Aichi-ken, Japan
Research Site
Yoshida-gun, Fukui, Japan
Research Site
Fukuoka, Fukuoka, Japan
Research Site
Maebashi, Gunma, Japan
To assess the safety and tolerability of AZD1152 in patients with AML by assessment of AEs, vital signs, ECG parameters, clinical chemistry, haematology (including clotting parameters) and urinalysis
Time frame: assessed at each visit
To examine the pharmacokinetics of AZD1152
Time frame: assessed after dose administration
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Research Site
Isehara, Kanagawa, Japan
Research Site
Yokohama, Kanagawa, Japan
Research Site
Chūō, Tokyo, Japan