Study identifier:D0110C00016
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase I, Randomised, 4-period Crossover, Open-label, Single-centre Study in Healthy Male Subjects to Assess the Pharmacokinetics of Orally Dosed Controlled Release Formulations of AZD5438 (40 mg)
solid tumour
Phase 1
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Interventional
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Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
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AstraZeneca
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No locations available
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