Phase I AZD2171 in Patients With Relapsed or Refractory AML and Elderly Patients With DeNovo or Secondary AML
NCT00502385 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 54
Last updated 2011-01-21
Summary
The study will be conducted across multiple European centres to assess the safety and tolerability of multiple doses of AZD2171 in patients with AML.
Conditions
- Leukaemia
- Myelocytic
- Acute
Interventions
- DRUG
-
AZD2171
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Nick Botwood, BSc, MBBS, MRCP, MFPM · AstraZeneca
-
Dieter Hoelzer, MD, PhD · Frankfurt University Hospital
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2004-04-30
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