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Research Study Evaluating an Investigational Weight-Loss Medication Clinical Trial for Adults with Obesity or Who Are Overweight and Related Health Conditions

Clinical Trial for Adults with Obesity or Who Are Overweight and Related Health Conditions

Study Information:

Obesity is a chronic medical condition that can affect overall health and increase the risk of developing conditions such as high blood pressure, high cholesterol, sleep apnoea, cardiovascular disease, and fatty liver disease.

Researchers are studying an investigational medicine designed to evaluate whether it, when combined with healthy eating and regular physical activity, may help support long-term weight management. This study will examine the investigational medicine's safety, tolerability, and its effects on health and wellbeing over time.

Who is it for?

You may be eligible if you:

  • Are aged 18 years or older
  • Have a BMI of 30 kg/m² or higher

OR

  • Have a BMI of 27 kg/m² or higher and at least one weight-related health condition, such as:
    • High blood pressure
    • High cholesterol
    • Sleep apnoea
    • Cardiovascular disease
    • Fatty liver disease (MASLD)
  • Have previously tried to lose weight through dietary measures without long-term success
  • Are not currently taking a GLP-1
  • Are willing and able to attend scheduled study visits and assessments
  • Are willing and able to self-administer a weekly injection

What does study participation look like?

If eligible, participation in the main study will last approximately 79 weeks, including screening, treatment, and follow-up. Participants who complete the main study may also be eligible to continue into an Open-Label Extension (OLE), where all participants receive the investigational medicine, subject to meeting the study requirements.

Participants will be randomly assigned to receive either the investigational medicine or placebo. Neither participants nor the study team will know which treatment has been assigned during the study.

The study treatment is self-administered once weekly as an injection under the skin using an autoinjector device.

Researchers will closely monitor participants' health, wellbeing, and safety throughout the study. Study procedures may include physical examinations, blood tests, ECGs, body measurements, questionnaires, and other health assessments.

Clinic visits will take place during business hours of 9am–5pm, Monday–Friday. Visit lengths may vary depending on the assessments required at each visit.