zovaglutide Arm 1
DrugZovaglutide will be administered via subcutaneous (SC) injection.
Other names: ZT002 Injection
NCT Number: NCT07812597
The main purpose of this study is to evaluate the safety and tolerability of continuing treatment with zovaglutide injection following titration to 2.4 mg semaglutide injection in adult participants with obesity.
Trial opening soon.
Get Notified18 year–75 year
All sexes
Interventional
Phase 2
Beijing Friendship Hospital, Capital Medical University, Beijing, Beijing Municipality, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Zovaglutide will be administered via subcutaneous (SC) injection.
Other names: ZT002 Injection
Zovaglutide will be administered via subcutaneous (SC) injection.
Other names: ZT002 Injection
Semaglutide will be administered via subcutaneous (SC) injection.
Time frame: from week 20 (randomization) to week 36
Measure description:Definition of successful switch: Participants administered the target dose of assigned zovaglutide at both week28 and week32.
Time frame: from week 20 (randomization) to week 36
Time frame: from week 20 (randomization) to week 36
Time frame: from week 20 (randomization) to week 40
Time frame: from week 20 (randomization) to week 40
Time frame: from week 20 ( randomization) to week 36
Trial opening soon.
Get NotifiedBeijing QL Biopharmaceutical Co.,Ltd
Industry
A Multicenter, Randomized, Active-Controlled, Open-Label Phase IIb Study Evaluating Safety and Tolerability of Switching to Zovaglutide Injection After Titration to 2.4 mg Semaglutide Injection (Wegovy®) in Adults With Obesity (HORIZON-SWITCH-SZ)
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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