phase I
enrolling

The Antibody Research Study

For healthy adults aged 18–60 in good physical and mental health with a BMI between 18 and 32. Conducted at our Morayfield clinic in Moreton Bay and in the Maroochy Private Hospital clinic in Maroochydore.
Age 18-60
day and overnight
Up to $13200
About this trial

If you are healthy, help advance new treatments

Coeliac disease, vitiligo, and alopecia areata are all autoimmune conditions, meaning the immune system mistakenly attacks the body's own cells and tissues. Together they affect hundreds of thousands of Australians, yet effective long-term treatments remain limited for many people living with these conditions.

This study is evaluating a new investigational antibody that may one day help treat all three conditions. Before it can progress to patient trials, researchers need to understand how healthy adults process and respond to it under closely monitored conditions.

By taking part as a healthy volunteer for an antibody research study, you are contributing to scientific development that could meaningfully improve the lives of people living with these conditions.

This study does not require a diagnosis of coeliac disease, vitiligo, or alopecia areata. It is open to healthy adults aged 18–60 who meet the eligibility criteria and are comfortable with a monitored clinic stay at our Morayfield clinic in Moreton Bay and the Maroochy Private Hospital clinic in Maroochydore.

Important update: We paused enrollment at our Morayfield clinic. New dates will be announced soon.
This study has two groups with different commitments and reimbursements: Group A involves a 5-night confinement stay over 3 months (up to $6,000), while Group B involves four confinement periods over 3.5 months (up to $13,200). Three out of four participants receive the investigational treatment rather than a placebo.
Eligibility

Do you qualify for an antibody research study?

Aged 18–60
BMI between 18.0 and 32.0
Generally, in good physical and mental health
No food allergies or dietary restrictions
No current smoker. Very light smoker may be considered for the study
What's involved

Commitment and procedures

Visit type
day and overnight
total visits
4-5
duration
~3.5 months
treatment
Single injection

procedures

Blood and urine tests
ECG (electrocardiogram)
Vital signs and physical examinations
PK, PD and immunogenicity (ADA) blood sampling
Injection site checks (subcutaneous cohorts)
Infusion reaction monitoring (intravenous cohort)

treatment design

The investigational antibody is administered on Day 1 either by injection under the skin or by intravenous (IV) infusion, depending on cohort assignment. This is a randomised, double-blind, placebo-controlled antibody research study with a 3:1 ratio, meaning three out of four participants receive the investigational medicine, and one out of four receives a placebo.
Neither participants nor study staff know the assignment. 

Group A participants complete a 5-night confinement period, followed by 3-month follow-up visits for our Morayfield and Maroochydore clinics.

Group B participants complete four confinement periods: 5 consecutive days followed by 16 days, plus a follow-up period lasting 3.5 months. Participants in this group will only take part in the Morayfield clinic.  

All procedures will be explained clearly, and participants can ask questions at any time.
More information

Have questions? We're here to help.

Contact our recruitment team directly, they're happy to answer any questions before you apply. Please do not send personal medical information by email.
Phone
+07 5409 8640
Hours
Mon–Fri, 8am–5pm
Trial at a glance
Status
enrolling
Phase
phase I
Therapeutic Area
Ages
18-60
Duration
~3.5 months
Visits
5 nights + follow-up visits
Location
Morayfield and Maroochydore clinics
PROTOCOL
FB102-102
Reimbursement
Up to $13200

Ready to check your eligibility?

Takes less than 2 minutes to complete the healthy volunteer trial form. 
Apply for this trial →
We won't share your details with third parties.
This trial has been reviewed by an independent human research ethics committee.

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