Study identifier:D0110C00008
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase I, Single-Blind, Randomised, Placebo-Controlled, 5 Period Cross-Over Study to Determine the Effect of Pre-Treatment with Oral or Intravenous Anti-Emetic on the Safety, Tolerability and Pharmacokinetics of a Single Oral Dose of AZD5438 in Healthy Male Volunteers
solid tumour
Phase 1
-
-
-
-
Interventional
-
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
-
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|