The Panorama Study

Currently Recruiting

18 May 2026

Up to $9,390

Melbourne, Australia

Autoimmune diseases happen when the body mistakenly produces harmful antibodies that attack its own organs and tissues. There are around 100 of these diseases, affecting about 240 million people globally.  This study aims to create more effective and accessible potential medication for millions of people across the globe. 

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Join our clinical trial

Autoimmune diseases happen when the body mistakenly produces harmful antibodies that attack its own organs and tissues. There are around 100 of these diseases, affecting about 240 million people globally. Although some treatments exist, there’s still a big need for better, targeted options, especially ones that are easy to take, like oral medications. 

Most advanced treatments today are given through IV or under the skin. These methods can be inconvenient and affect a patient’s quality of life. That’s why an oral treatment like the study drug could be a game-changer, making treatment easier and more appealing, especially for people who prefer to avoid needles. This study aims to create more effective and accessible potential medication for millions of people across the globe. 

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.

Join our clinical trial image

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

Administered via oral tablet.

Ethics

An independent ethics committee has approved this clinical trial. 

Additional eligibility

  • Weight above 50kg
  • Non-smoker and has not smoked for at least 6 months prior to screening

Study duration

2 sets of 9 nights stay,
1 follow-up visit

Are you a match?

Age

18 - 55 years old

Remuneration

Up to $9,390 *with screening reimbursement. Please see T&Cs.

Gender

Male or Female (Post-menopausal)

BMI

BMI 18 - 32 kg/m2

Commitment

18 nights, 1 clinic visit

Medical condition

Not taking any medications

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?
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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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