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

Study identifier:D8750C00008

ClinicalTrials.gov identifier:NCT07220954

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A Phase I, Single-Dose, Open-Label, Sequential, Randomised, Crossover Study to Assess the Relative Bioavailability of Different Subcutaneous Formulations of AZD6234 in Participants Living with Overweight or Obesity

Medical condition

Healthy Participants

Phase

Phase 1

Healthy volunteers

Yes

Study drug

AZD6234 Formulation 1, AZD6234 Formulation 2 (low concentration), AZD6234 Formulation 2 (high concentration), AZD6234 Formulation 3

Sex

All

Actual Enrollment

19

Study type

Interventional

Age

18 Years - 55 Years

Date

Study Start Date: 11 Nov 2025
Primary Completion Date: 16 Sept 2026
Study Completion Date: 16 Sept 2026

Study design

Allocation: Randomized
Endpoint Classification: -
Intervention Model: Crossover Assignment
Masking: -
Primary Purpose: Treatment

Verification:

Verified 01 Oct 2026 by AstraZeneca

Sponsors

AstraZeneca

Collaborators

Quotient Sciences Limited

Inclusion and exclusion criteria