The Linden Study

Currently Recruiting

6 May to 13 May 2026

Up to $2,900

Brisbane, Australia

The study drug is being developed as a potential treatment to support people living with obesity and assist with weight management. While current treatments can be effective, they do not work well for everyone and may cause side effects such as nausea, vomiting, and other gastrointestinal symptoms.

This investigational treatment is designed to offer a different approach. Rather than focusing solely on overall weight reduction, it aims to help regulate appetite while supporting a healthier balance between fat mass and lean muscle mass. By targeting body composition as well as weight, the study drug may provide an alternative option for individuals who have not responded well to existing treatments.

Apply now Speak with us 1300 781 355

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. It is not known whether the study drug may cause unexpected, serious, or life-threatening side effects. While these are considered unlikely, you will be carefully monitored throughout the study and provided with prompt treatment if any such effects occur.

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

Why participate?

  • Participation in a monitored clinical environment
  • Scheduled study visits
  • Support from a professional medical team
  • Reimbursement for your time and commitment

Trial details

Study duration

  • 4 nights stay
  • 1 follow-up visit

Study medication

Administered via oral solution.

Ethics

An independent ethics committee has approved this clinical trial. 

Additional eligibility

  • Non-smokers or smoking no more than 5
    cigarettes per week

Are you a match?

Age

18 - 55 years old

Remuneration

Up to $2,900 *with screening reimbursement. Please see T&Cs.

Gender

Male, Female or Female (Post-menopausal)

BMI

BMI 25 - 40 kg/m2

Commitment

4 nights, 1 clinic visit

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


What is your date of birth?
Day Month Year

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



Consent to Information Use and Future Contact