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Clinical Trial Summary

This study will evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of single and multiple ascending doses of AZD4144 administered orally in healthy participants.


Clinical Trial Description

This is a Phase I, first time-in human (FTiH), randomised, single-blind, placebo-controlled, single ascending dose (SAD) and multiple ascending dose (MAD) sequential group study in healthy participants. Part A consists of 3 parts: Part A1 (healthy participants) Part A2 (healthy Japanese participants) and Part A3 (healthy Chinese participants) Part B consists of 2 parts: Part B1 (healthy participants) Part B2 (healthy Japanese participants) Both Part A and Part B of the study will comprise of a screening period of maximum 28 days. The treatment period would last from Day -1 to Day 4 in Part A and from Day -1 to Day 15 in Part B of the study. A follow up visit will be performed on Day 10 + 3 days for Part A and on Day 20 + 3 days for Part B. Each participant will participate for about 6 weeks in Part A of the study and for about 7 weeks in Part B of the study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06122714
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 7, 2023
Completion date October 17, 2024

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