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Clinical Trial Summary

This study will assess the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of AZD2389 following single and multiple dose administration (SAD/MAD) to healthy participants.


Clinical Trial Description

This is a Phase I, First In Human (FIH), randomized, single-blind, placebo-controlled, single and multiple ascending dose study in healthy male and/or female participants of non-childbearing potential including healthy participants of Chinese and Japanese ethnicity performed at a single center. The study consists of 2 parts: Part A and Part B. 72 participants have been planned for Part A and 32 participants for Part B. Each participant in Part A will be involved in the study for up to 6 weeks, and each participant in Part B will be involved in the study for up to 8 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06138795
Study type Interventional
Source AstraZeneca
Contact AstraZeneca Clinical Study Information Center
Phone 1-877-240-9479
Email information.center@astrazeneca.com
Status Recruiting
Phase Phase 1
Start date November 20, 2023
Completion date November 4, 2024

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