Study identifier:D8750C00009
ClinicalTrials.gov identifier:NCT07017179
EudraCT identifier:N/A
CTIS identifier:N/A
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
Obesity/Overweight
Phase 2
No
AZD6234, Placebo
All
871
Interventional
18 Years - 55 Years
Allocation: Randomized
Endpoint Classification: -
Intervention Model: Parallel Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 Jul 2025 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: AZD6234 (sub-study 1) Participants will receive subcutaneous injection of AD6234 on Day 1 and continue for 16 weeks. | Drug: AZD6234 Participants will receive a subcutaneous injection weekly |
Placebo Comparator: Placebo (sub-study 1) Participants will receive subcutaneous injection of matched volume of placebo on Day 1 and continue for 16 weeks. | Drug: Placebo Participants will receive a subcutaneous injection weekly. |