drugset / Trial / NCT07222254

A Study to Assess the Safety, Tolerability, and Pharmacokinetics of a Single Ascending Dose of AZD0292 in Healthy Japanese Participants

NCT07222254 ↗

Phase 1 Active not recruiting 18 enrolled AstraZeneca
RandomizedSequentialQuadruple-blindTreatment

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.

Timeline

Start
2025-12-12
Primary completion
2026-07-20
Completion
2026-07-20

Drugs

EvaluationDrugModalityDoseRoute
Subject AZD0292 Monoclonal antibody — Intravenous

Indications

No indication recorded.