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A Study to Assess the Safety, Tolerability, and Pharmacokinetics of a Single Ascending Dose of AZD0292 in Healthy Japanese Participants
Sponsor: AstraZeneca
Summary
The purpose of the study is to evaluate the safety, tolerability and pharmacokinetics (PK) of single ascending doses of AZD0292 administered via intravenous (IV) infusion in healthy Japanese participants.
Official title: A Phase I, Randomized, Double-blind, Placebo-controlled Study to Assess the Safety, Tolerability, and Pharmacokinetics of AZD0292 Following Single Ascending Dose Administration to Healthy Japanese Participants
Key Details
Gender
All
Age Range
18 Years - 60 Years
Study Type
INTERVENTIONAL
Enrollment
18
Start Date
2025-12-12
Completion Date
2026-07-20
Last Updated
2026-03-05
Healthy Volunteers
Yes
Conditions
Interventions
AZD0292
Single dose of AZD0292 will be administered as an IV infusion.
Placebo
Single dose of placebo will be administered as an IV infusion.
Locations (1)
Research Site
Sumida-ku, Japan