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This is a Multi-centre, Multi-drug, Platform Study in Chinese Participants Living With Obesity / Overweight
Sponsor: AstraZeneca
Summary
This study is to assess the safety and tolerability, PK characterisation, efficacy, and immunogenicity of the study intervention, and it allows assessment of the monotherapy or combination therapy of AZD6234 and AZD9550 in different sub-studies.
Official title: A Phase IIa Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of AZD6234, AZD9550, and AZD6234 in Combination With AZD9550 in Chinese Participants Living With Obesity/Overweight
Key Details
Gender
All
Age Range
18 Years - 55 Years
Study Type
INTERVENTIONAL
Enrollment
871
Start Date
2025-05-20
Completion Date
2026-08-06
Last Updated
2026-01-27
Healthy Volunteers
No
Conditions
Interventions
AZD6234
Participants will receive a subcutaneous injection weekly
Placebo
Participants will receive a subcutaneous injection weekly.
AZD9550
Participants will receive a subcutaneous injection weekly
Plocebo
Participants will receive a subcutaneous injection weekly
AZD6234 in combination with AZD9550
Participants will receive a subcutaneous injection weekly
Placebo
Participants will receive a subcutaneous injection weekly
Locations (3)
Research Site
Jinan, China
Research Site
Nanjing, China
Research Site
Shanghai, China