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NCT07812597Not yet recruitingPhase 2

A Study Evaluating Safety and Tolerability of Switching From Semaglutide to Zovaglutide in Adults With Obesity (HORIZON-SWITCH-SZ)

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)

Source: ClinicalTrials.gov · Last updated 10 Sept 2026

Brief summary (registry, in English)

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.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
210 (estimated)
First submitted
31 Aug 2026
Start date
12 Oct 2026
Primary completion date
13 Jan 2028
Lead sponsor
Beijing QL Biopharmaceutical Co.,Ltd
Diseases
Obesity
NCT number
NCT07812597

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 210
  • From 12 Oct 2026 to the primary completion date, 13 Jan 2028
  • 16 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previously diagnosed obesity caused by monogenic mutations, other diseases, or medications.
  • Used of medicines or treatments that affect weight within 3 months prior to screening.

Other illness

  • History of acute or chronic pancreatitis, or pancreatic injury.
  • History of medullary thyroid carcinoma (MTC) or type 2 multiple endocrine neoplasia (MEN2) in personal or family history.
  • History of medullary thyroid carcinoma (MTC) or type 2 multiple endocrine neoplasia (MEN2) in personal or family history.

Lab values

  • Previous diagnosis of diabetes; or HbA1c ≥ 6.5% or fasting blood glucose ≥ 7.0 mmol/L at screening.

Other

  • Patient Health Questionnaire-9 (PHQ-9) scale score is ≥ 15 at screening
  • Screening Columbia-Suicide Severity Rating Scale(C-SSRS) questionnaire suicide ideation response of "Category 4 or 5," or any "yes" response to suicidal behavior questions

Who the study is looking for

  • Male or female subjects aged≥18years and≤75 years at the time of signing the Informed Consent Form (ICF).
  • At screening, Body Mass Index (BMI)≥28kg/m²
  • Weight change due to diet and exercise alone within 3 months prior to screening did not exceed 5%.

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (16)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Peking University People's Hospital
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BeijingChinaUnknown status
Beijing Friendship Hospital, Capital Medical University
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BeijingChinaUnknown status
Jilin Province FAW General Hospital
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ChangchunChinaUnknown status
The First People's Hospital of Changde
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ChangdeChinaUnknown status
The 2nd People's Hospital of Chengdu
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ChengduChinaUnknown status
Handan First Hospital
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HandanChinaUnknown status
Harbin Medical University Affiliated Fourth Hospital
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HarbinChinaUnknown status
Huizhou Central People's Hospital
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HuizhouChinaUnknown status
Central Hospital Affiliated to Shandong First Medical University
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JinanChinaUnknown status
Jincheng General Hospital
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JinchengChinaUnknown status
Hebei Petro China Cental Hospital
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LangfangChinaUnknown status
The First Affiliated of Nanyang Medical College
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NanyangChinaUnknown status
The Fifth People's Hospital of Shenyang
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ShenyangChinaUnknown status
Yichang Central People's Hospital (Xiling Campus)
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YichangChinaUnknown status
Zibo Municipal Hospital
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ZiboChinaUnknown status
Zibo Central hospital
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ZiboChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.