Study identifier:D1531C00008
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A phase I, open label, multi-centre study to assess the safety, tolerability, and pharmacokinetics of AZD1152 in Japanese patients with acute myeloid leukaemia.
Acute Myeloid Leukaemia
Phase 1
No
AZD1152
All
30
Interventional
20 Years +
Allocation: Non-randomized
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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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.
Location
Location
Maebashi-city, Gunma, Japan
Location
NAGOYA, Aichi, Japan
Location
Chuo, Tokyo, Japan
Location
YOSHIDA-GUN, Fukui, Japan
Location
FUKUOKA, Fukuoka, Japan
Location
ISEHARA, Kanagawa, Japan
Location
YOKOHAMA, Kanagawa, Japan
Arms | Assigned Interventions |
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