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Clinical Trial Summary

This Phase I, randomised, single-blind, placebo-controlled study has been designed to assess the safety, tolerability, and pharmacokinetics (PK) of AZD2693 following subcutaneous (SC) administration of AZD2693 in healthy participants


Clinical Trial Description

The study will be performed at a single study center in Japan. The study will comprise of following periods: - Screening Period of maximum 28 days. - An 8-week Treatment Period during which participants will be randomized to receive multiple doses of AZD2693 or placebo at the study center. - A Follow-up Period of 15 weeks post last dose of study intervention consisting of 8 Follow-up Visits. Participants will be enrolled in 4 consecutive cohorts of 11 participants where 8 participants will be randomized to receive AZD2693 and 3 participants will be randomized to receive placebo. A participant is considered to have completed the study if the participant has completed all phases of the study including the last visit. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05107336
Study type Interventional
Source AstraZeneca
Contact
Status Completed
Phase Phase 1
Start date November 25, 2021
Completion date March 21, 2023

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