ICI176,334-1
DrugSubject will receive single dose of ICI176,334-1
NCT Number: NCT01415778
The purpose of this study is to investigate the bioequivalence of ICI176,334-1 in Japanese healthy male subjects.
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Notify Me20 year–45 year
Male
Interventional
Phase 1
Bioequivalence study of ICI176,334-1 in Japanese healthy male subjects - evaluation of bioequivalence of ICI176,334-1 and Casodex 80 mg tablet -
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Subject will receive single dose of ICI176,334-1
Subject will receive single dose of Casodex 80 mg tablet
Time frame: Blood samples are taken repeatedly for 72 hours and also taken occasionally up to 672 hours after each dose period
Time frame: Blood samples are taken repeatedly for 72 hours and also taken occasionally up to 672 hours after each dose period
Time frame: Blood samples are taken repeatedly for 72 hours and also taken occasionally up to 672 hours after each dose period
Time frame: Blood samples are taken repeatedly for 72 hours and also taken occasionally up to 672 hours after each dose period
Time frame: Screening day up to 35 to 42 days (follow-up)
Time frame: Collect prior to treatment and up to 35 to 42 days (follow-up) after the last dose.
Time frame: Collect prior to treatment and up to 35 to 42 days (follow-up) after the last dose.
AstraZeneca
Industry
Bioequivalence Study of ICI176,334-1 in Japanese Healthy Male Subjects - Evaluation of Bioequivalence of ICI176,334-1 and Casodex 80 mg Tablet -
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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