The Body Balance Study

Currently Recruiting

2 Dec to 4 Dec 2025

Up to $11,150

This study is testing a new treatment for weight management. The study drug is designed to support healthier weight management by targeting several key areas of the body’s metabolism.

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Join our clinical trial

This is a first-in-human (FIH) study, meaning it is the first time the potential treatment is being tested in people. The study has been carefully designed with strict safety protocols and has been approved by an independent ethics committee. 

Before joining, you’ll receive detailed information about the study, meet with a doctor, and have the chance to ask any questions. 

This study is testing a new treatment for weight management. The study drug is designed to support healthier weight management by targeting several key areas of the body’s metabolism. It aims to reduce excess fat mass while helping preserve lean muscle, which is essential for strength and long-term health. By improving insulin sensitivity, the drug may also promote better blood sugar control, while fostering favourable lipid profiles that support heart health. In addition, the treatment is being studied for its potential to reduce inflammation within fat tissue, which can contribute to improved overall metabolic function and wellbeing. 

This study drug is important because many current obesity treatments come with significant limitations, such as only modest weight loss, unwanted loss of lean muscle, unpleasant gastrointestinal side effects, or rapid weight regain once treatment stops. By addressing these challenges, the drug aims to provide a more effective and sustainable approach to supporting long-term weight management and overall health. 

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Why participate?

  • Contribute to Research that supports communities across the globe
  • Help Make Treatments More Inclusive and Effective 
  • Be the Reason Better Treatments Move Forward 

Trial details

Study medication

The study drug is administered via a subcutaneous injection (a small injection given into the fatty tissue of the abdomen)

Ethics

An independent ethics committee has approved this clinical trial. 

Additional eligibility

  • BMI between 27 and 40kg/m²  
  • Participants of Asian descent: BMI of at least 23 kg/m2
  • Participants of non-Asian descent: BMI of at least 27 kg/m2
  • Weight stability in the past 3 months 
  • Non-smokers and no tobacco or nicotine use during your stay 
  • No current medication use (with some exceptions as discussed with our medical team) 
  • No serious medical conditions  
  • Not pregnant or breastfeeding 
  • Willing to follow contraception guidelines (if applicable) 
  • Able to attend all study visits and follow instructions 

Study duration

2-night in-clinic stay and 10 follow-up visits

Are you a match?

Age

18 - 65 years old

Remuneration

Up to $11,150 *with screening reimbursement. Please see T&Cs.

Gender

Male or Female

BMI

BMI 27 - 40 kg/m2

Commitment

2 nights, 10 clinic visits

Register Your Interest

This form takes around 3–5 minutes to complete. Your information will remain confidential and is used only to assess your eligibility for current or future research studies.
Step 1 of 3
Contact Information




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Nucleus Network does not currently conduct clinical trials in your state. If you would like to receive study information should this situation change, please complete and submit this form.
Personal Information

This includes registering your interest with the Centre for Clinical Studies, Q-Pharm or Nucleus Network

Please call us on 1800 243 733 or schedule a call.


What is your date of birth?
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You need to be at least 18 years old to participate in clinical trials.


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Step 2 of 3
Medical History

We regularly have studies that allow participants who are (social) smokers.

We define an allergy as severe if symptoms include mouth/throat/face swelling, shortness of breath or a whole-body rash, or if it required hospitalisation

We regularly have studies that allow for/require participants with asthma.



We regularly have studies that allow for/require participants with medical conditions.

Medications & Contraception Requirements

We regularly have studies that allow participants with depression that is well-managed on a stable dose of medication.

If the only prescription medication you currently use is hormonal contraception and/or Ventolin, please select No above. We regularly have studies that allow for participants who take a stable dose of prescription medication.


  • Abstinence from sex with anyone of the opposite sex for at least 2 months
  • Using a condom + your female sexual partner(s) using a separate form of birth control
  • You or your sexual partner(s) had a vasectomy/hysterectomy
  • Your sexual partner(s) are post-menopausal


Only you taking birth control or your partner(s) using a condom is not an acceptable option, but using both together is. The morning after pill is not an acceptable form of birth control.

  • Abstinence, by choice, from sex with anyone of the opposite sex for the last 2 months + remaining abstinent for at least 2 months after study participation
  • You using birth control + your male sexual partner(s) using a condom
  • You or your sexual partner(s) had a hysterectomy/vasectomy
  • You are post-menopausal



Step 3 of 3
Study Preferences

While longer studies generally have a higher reimbursement, there are also studies with multiple short stays that have high reimbursements.
Referral Information



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