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NCT05890976CompletedPhase 3

Research Study Looking at How Well Semaglutide Tablets Taken Once Daily Work in Chinese Adults Who Are Above a Healthy Weight Range (OASIS 3)

Efficacy and Safety of Oral Semaglutide 50 mg Once Daily in Chinese Adults With Overweight or Obesity (OASIS 3)

Source: ClinicalTrials.gov · Last updated 22 Jan 2026

Brief summary (registry, in English)

This study is being conducted to see if semaglutide tablets can be used as a treatment to help people who are above a healthy weight range to lose weight. Semaglutide tablets are a new medicine being tested to treat people living with excess body weight. Participants will either get semaglutide or placebo once daily morning for 44 weeks. In addition to taking the medicine, participants will have talks with study staff about: * Healthy food choices * How to be more physically active * What participants can do to lose weight This study will last for about 1 year.

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
200 (actual)
First submitted
26 May 2023
Start date
30 May 2023
Primary completion date
16 Jan 2025
Lead sponsor
Novo Nordisk A/S
Diseases
Obesity
NCT number
NCT05890976

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 200
  • From 30 May 2023 to the primary completion date, 16 Jan 2025
  • 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

  • Uncontrolled and potentially unstable diabetic retinopathy or maculopathy. Verified by a fundus examination performed by an ophthalmologist or another suitably qualified health care provider within the past 90 days prior to screening or in the period between screening and randomisation. Pharmacological pupil-dilation is a requirement unless using a digital fundus photography camera specified for non-dilated examination.

Other illness

  • History of type 1 or type 2 diabetes.

Lab values

  • HbA1c greater than or equal to 6.5 percent (48 mmol/mol) as measured by the central laboratory at screening.
  • Treatment with glucose-lowering agent(s) within 90 days prior to screening.
    • Participants with T2D at screening:
  • Renal impairment measured as estimated glomerular filtration rate (eGFR) value of lesser than 30 milli litre per min/1.73 square metre (mL/min/1.73 m\^2) according to Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) creatinine equation as defined by Kidney Disease Improving Global Outcomes (KDIGO) 2012 classification by the central laboratory at screening.

Other

  • Participants without T2D at screening:

Who the study is looking for

  • Informed consent obtained before any study-related activities. Study-related activities are any procedures that are carried out as part of the study, including activities to determine suitability for the study.
  • Male or female, age greater than or equal to 18 years at the time of signing informed consent.
  • Body mass index (BMI) of
    • greater than or equal to 28.0 kilogram per meter square (kg/m\^2) or
    • greater than or equal to 24.0 kg/m\^2 with greater than or equal to 1 weight-related comorbidity (treated or untreated). Weight-related comorbidities should be hypertension, T2D, dyslipidaemia, obstructive sleep apnoea or cardiovascular disease.
  • History of at least one self-reported unsuccessful dietary effort to lose body weight.
    • For participants with T2D at screening the following inclusion criteria apply in addition to criteria 1- 4:
  • Diagnosed with T2D greater than or equal to 180 days prior to screening.
  • Treated with either diet and exercise alone or stable treatment (same drug(s) or active ingredient, dose and dosing frequency) for at least 60 days prior to the day of screening with up to 3 oral antidiabetic drugs (OAD)s alone or in any combination (metformin, α-glucosidase (AGI), sulphonylureas (SU), glinides, SGLT2i (sodium-glucose co-transporter 2 inhibitor) or glitazone).
  • HbA1c 7.0 - 10.0 percent (53 - 86 millimoles per mole \[mmol/mol\]) (both inclusive) as measured by central laboratory at screening.

Age in the registry: 18 years to - · 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-Endocrinology
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BeijingChinaUnknown status
Beijing Friendship Hospital, Capital Medical University-Endocrinology
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BeijingChinaUnknown status
The First People's Hospital of Changde City-Endocrinology
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ChangdeChinaUnknown status
Changzhou No.2 People's Hospital
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ChangzhouChinaUnknown status
Chongqing University Three Gorges Hospital
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ChongqingChinaUnknown status
Huizhou Central People's Hospital-Endocrinology
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HuizhouChinaUnknown status
Jinan Central Hospital
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Ji'nanChinaUnknown status
Jinan Central Hospital
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JinanChinaUnknown status
Huaihe Hospital of Henan University-Endocrinology
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KaifengChinaUnknown status
The First Affiliated Hospital of Henan University of Science and Technology
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LuoyangChinaUnknown status
The Second Affiliated Hospital of Nanjing Medical University
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NanjingChinaUnknown status
Shanghai Pudong New Area People's Hospital-Endocrinology
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ShanghaiChinaUnknown status
Huashan Hospital Fudan University-Endocrinology
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ShanghaiChinaUnknown status
Taihe Hospital-Endocrinology
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ShiyanChinaUnknown status
General Hospital of Tianjin Medical University-Endocrinology
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TianjinChinaUnknown status
The Affiliated Hospital of Jiangsu University
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ZhenjiangChinaUnknown status

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