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Trial · Interventional

Not yet recruitingPhase 4Registry data

A Randomized Controlled Study of Dose-tapering Regimen of Semaglutide for Weight-Loss Maintenance in Adults With Overweight or Obesity

Overview

Status
Not yet recruiting
Phase
Phase 4
Enrollment
72 participants (estimated)
Sponsor
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology · Other
Design
Randomized · Open label (no masking)
Countries
Not stated
Start
1 Sept 2026 (estimated)
Primary completion
30 Dec 2027 (estimated)
Completion
30 Jun 2029 (estimated)
First posted
25 Aug 2026
Last update posted
25 Aug 2026
Conditions
Obesity & Overweight

Timeline

1 trial · 1 not yet recruiting

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
20262027202820292030
  1. Ph 4

    A Randomized Controlled Study of Dose-tapering Regimen of Semaglutide for Weight-Loss Maintenance in Adults With Overweight or Obesity

    NCT07783854

    est. 1 Sept 2026 to est. 30 Jun 2029

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

The goal of this clinical trial is to determine whether a semaglutide dose-tapering regimen is non-inferior to a treatment-dose maintenance regimen for weight-loss maintenance in adults with overweight or obesity who have achieved stable weight loss. This trial will also evaluate the safety of the dose-tapering regimen. The primary research questions are: Is the semaglutide dose-tapering regimen non-inferior to the treatment-dose maintenance regimen for weight-loss maintenance at 24 weeks? Can the dose-tapering regimen alleviate adverse events and offer a more personalized, sustainable pathway for medication discontinuation? Researchers will compare the semaglutide dose-tapering regimen against a treatment-dose maintenance regimen to assess whether the tapering strategy preserves weight loss and improves cardiometabolic markers. Participants will: Be randomly assigned to receive either the semaglutide dose-tapering regimen or the treatment-dose maintenance regimen for 24 weeks. Complete a 24-week follow-up period after medication discontinuation (48 weeks total study duration). Attend scheduled clinic visits for physical examinations and laboratory testing to assess weight, BMI, waist circumference, cardiometabolic markers (including blood glucose, blood pressure, and lipids), and to monitor adverse events.

Interventions

  • Semaglutide Dose-Tapering RegimenDrug
  • Semaglutide Maintenance-Dose RegimenDrug

Arms2

  • Experimental

    Dose-tapering Group

    Participants receive a semaglutide dose-tapering regimen, starting from their stable entry dose of 1.7 mg/week. A 25% dose reduction is implemented every 8 weeks until the end of week 24.

  • Active comparator

    Maintenance-dose Group

    Participants maintain their original stable entry regimen of semaglutide 1.7 mg once weekly throughout the 24-week intervention period, with no dose adjustments performed.

Primary outcomes1

Outcomes the sponsor listed as primary.

  1. Percentage change in body weight from baseline to week 24

    Time frame · Baseline (Week 0) to Week 24

    Registry description

    Body weight is measured with a calibrated medical electronic scale (accurate to 0.1 kg). Subjects are weighed in the morning after an overnight fast, post-voiding, barefoot, and wearing light clothing. Percentage change is calculated as \[(Week 24 body weight - baseline body weight) / baseline body weight\] × 100%.

Secondary outcomes(3)
  1. Absolute change in body weight from baseline to week 24 (kg)

    Time frame · Baseline (Week 0) to Week 24

    Registry description

    Measured using a calibrated medical electronic scale (accurate to 0.1 kg). Subjects will be weighed in the morning after an overnight fast, post-voiding, barefoot, and wearing light clothing. The absolute difference between baseline and week 24 body weight will be calculated.

  2. Mean change in waist circumference from baseline to week 24 (cm)

    Time frame · Baseline (Week 0) to Week 24

    Registry description

    Measured using a non-stretchable standard measuring tape (accurate to 0.1 cm). Waist circumference will be measured at the midpoint between the lower margin of the last palpable rib and the top of the iliac crest in the mid-axillary line at the end of a normal expiration. The change from baseline is calculated.

  3. Mean change in body mass index (BMI) from baseline to week 24 (kg/m²)

    Time frame · Baseline (Week 0) to Week 24

    Registry description

    Height is measured using a standard stadiometer (accurate to 0.1 cm). Combined with the weight measured at the same timepoint, BMI is calculated using the formula: weight (kg) / height (m)².

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

No results are posted for this trial.

A trial that is still running, or that stopped early, may post results later.

Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works

Studies0

Studies that cite this trial.

No study cites this trial.

Eligibility

Who could join, as posted.

Sex
All
Age
from 18 Years up to 64 Years
Healthy volunteers
Not accepted
Inclusion and exclusion criteria, as posted
Inclusion Criteria: * Men and women, aged 18 to 64 years inclusive at the time of signing the informed consent form. * Ongoing weight-loss treatment consisting of weekly semaglutide, with a documented weight reduction of ≥ 10% of pre-treatment body weight, or a weight reduction between 5% and \< 10% concurrent with a BMI \< 25 kg/m². * Maintained on a weekly semaglutide dose of 1.7 mg, with a stable weight over the 12 weeks prior to enrollment (less than 5% change in body weight). * Voluntarily participating in the study, capable of effective communication with the investigators, willing to comply with all study procedures, and having provided written informed consent. Exclusion Criteria: * History or planned bariatric surgery or use of a weight-loss device during the trial. * Obesity induced by other endocrinologic disorders or monogenic mutations, including but not limited to hypothalamic obesity, pituitary obesity, hypothyroidism, Cushing's syndrome, insulinoma, acromegaly, or hypogonadism. * Glycated hemoglobin (HbA1c) ≥ 6.5% as measured by a local laboratory at screening, or a history of diabetes mellitus (excluding a history of gestational diabetes). * Use of any weight-loss medications (e.g., tirzepatide, mazdutide, liraglutide, orlistat, sibutramine, phenylpropanolamine, chlorpheniramine, phentermine, lorcaserin, phendimetrazine, phentermine-topiramate, or naltrexone-bupropion), herbal medicines, dietary supplements, or meal replacements affecting body weight within 90 days prior to screening (except semaglutide and lifestyle interventions). Use of medications that may cause significant weight gain, including systemic glucocorticoids for more than 1 week, antipsychotics or antiepileptics (e.g., imipramine, amitriptyline, mirtazapine, paroxetine, phenelzine, chlorpromazine, clozapine, olanzapine, valproic acid and its derivatives, lithium preparations, thioridazine), or growth hormone. * History of acute or chronic pancreatitis, or presence of high-risk factors such as a history of pancreatic injury. Current or past history of malignancies (except for localized basal cell carcinoma of the skin, carcinoma in situ of the cervix, or carcinoma in situ of the prostate). Personal or family history of medullary thyroid carcinoma (MTC) or multiple endocrine neoplasia syndrome type 2 (MEN 2, including MEN 2A and MEN 2B). * End-stage renal disease, or requiring long-term/intermittent hemodialysis or peritoneal dialysis. * Occurrence of any of the following within 60 days prior to screening: myocardial infarction, stroke, hospitalization for unstable angina, or transient ischemic attack (TIA). * Current New York Heart Association (NYHA) class IV heart failure. * Known or suspected hypersensitivity to the investigational product or related products. * Participation in another clinical trial within 90 days prior to screening. * Female patients who are pregnant, breastfeeding, or planning to become pregnant within the next two years. * History of major depressive disorder or a diagnosis of other severe psychiatric disorders (e.g., schizophrenia, bipolar disorder) within 2 years prior to screening. * History of attempted suicide. * Abnormal laboratory results at screening: severe hepatic or renal impairment, such as aspartate aminotransferase (AST) or alanine aminotransferase (ALT) \> 2.5 × upper limit of normal (ULN); bilirubin \> 2.5 × ULN (except for known Gilbert's syndrome meeting the criteria of fractionated conjugated bilirubin \< 35% of total bilirubin); triglycerides ≥ 5.7 mmol/L. * Unstable proliferative retinopathy or maculopathy requiring urgent treatment within 1 year prior to screening, or a history of diabetic ketoacidosis, diabetic hyperosmolar nonketotic coma, or severe metabolic disorders leading to neurological or psychiatric dysfunction. * History or risk factors of the following: clinically significant anemia, epilepsy, syncope, cardiac arrest, arrhythmia, atrioventricular block, structural heart disease, or torsades de pointes. * Severe active bacterial, viral, or fungal infections requiring hospitalization or intravenous antibiotic therapy. * History of infectious diseases, including but not limited to HIV/AIDS, syphilis, or active infectious hepatitis. * History of alcohol dependence or substance abuse within 6 months prior to screening. * Any other condition that, in the opinion of the investigator, makes the patient unsuitable for participation in the study.

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