ICI176,334-1
DrugSubject will receive single dose of ICI176,334-1
NCT Number: NCT01415791
The purpose of this study is to investigate the presence or absence of oral mucosal absorption of ICI176,334-1
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Notify Me20 year–45 year
Male
Interventional
Phase 1
Oral mucosal absorption of ICI176,334-1 in Japanese healthy male subjects
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
Time frame: Samples are taken at 72 hours after application of the investigational drug
Time frame: Samples are taken at 168 hours after application of the investigational drug
Time frame: Samples are taken at 72 hours after application of the investigational drug
Time frame: Samples are taken at 168 hours after application of the investigational drug
Time frame: Adverse Events will be captured starting from screening up to 14 to 21 days (follow-up)
Time frame: Collect prior to treatment and up to 14 to 21 days (follow-up) after application of the investigational drug
Time frame: Collect prior to treatment and up to 14 to 21 days (follow-up) after application of the investigational drug
AstraZeneca
Industry
Oral Mucosal Absorption of ICI176,334-1 in Japanese Healthy Male Subjects
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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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