A Study to Assess the Relative Bioavailability of Different Subcutaneous Formulations ofAZD6234

Recruiting now · Phase 1

Conditions studied: Healthy Participants

In brief

This study in healthy volunteers aims to compare blood levels and side effects after administration of different formulations of AZD6234. This study will take place at one site in Nottingham, United Kingdom, and will enrol 21 healthy men and women aged 18-55 years.

Key facts

Study ID
NCT07220954
Run by
AstraZeneca
People needed
21
Starts
2025-11-11
Expected to finish
2027-04-01
Last updated by the study team
2026-05-18

Who can join

Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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