Safety, Tolerability and PK of AZD1152 in Patients with Relapsed Acute Myeloid Leukaemia (AML)
Study identifier:D1531C00008
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
Study Complete
Official Title
A phase I, open label, multi-centre study to assess the safety, tolerability, and pharmacokinetics of AZD1152 in Japanese patients with acute myeloid leukaemia.
Medical condition
Acute Myeloid Leukaemia
Phase
Phase 1
Healthy volunteers
No
Study drug
AZD1152
Sex
All
Actual Enrollment
30
Study type
Interventional
Age
20 Years +
Date
Study Start Date: 01 Nov 2007
Primary Completion Date: 01 Aug 2009
Study Completion Date: 01 Aug 2009
Study design
Allocation: Non-randomized
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Verification:
Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals
Sponsors
AstraZeneca Pharmaceuticals
Collaborators
-
Inclusion and exclusion criteria
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No locations available
| Arms | Assigned Interventions |
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Contacts
Investigators
Principal Investigator
Paul Stockman
AstraZeneca
