A Phase I, Open-label, Multicentre Study to Assess the Safety, Tolerability, Pharmacodynamics and Pharmacokinetics o fAZD5438 Given Orally, in 2 dosing schedules, in Patients with Advanced Solid Malignancies.
Study identifier:D0110C00003
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
Study Complete
Official Title
A Phase I, Open-label, Multicentre Study to Assess the Safety, Tolerability, Pharmacodynamics and Pharmacokinetics o fAZD5438 Given Orally, in 2 dosing schedules, in Patients with Advanced Solid Malignancies.
Medical condition
solid tumour
Phase
Phase 1
Healthy volunteers
-
Study drug
-
Sex
-
Actual Enrollment
-
Study type
Interventional
Age
-
Date
Study Start Date: 01 Jul 2004
Primary Completion Date: -
Study Completion Date: -
Study design
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verification:
-
Sponsors
AstraZeneca
Collaborators
-
Inclusion and exclusion criteria
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