
Eczema Studies Hutt Valley (H)
Hutt Valley
We are looking for adults aged 18–65 with moderate to severe atopic dermatitis (eczema) to take part in a clinical trial of an investigational medication (ZL‑1503) versus placebo. Eligible participants will receive three IV infusions every two weeks (Weeks 0, 2, and 4) and then attend clinic visits for health checks up until Week 52.
Description
What to expect
Ages
18-65 years
Duration
23 visits over 13 months
Compensation
You will be reimbursed for your time and travel costs
Eligibility Criteria
Locations
About the study
Taking part starts with meeting the research doctor to discuss your health and check eligibility. If eligible and you choose to participate, you’ll have 3 dosing visits (Weeks 0, 2, 4) and scheduled follow‑ups through Week 52. The overall duration of the study from start to finish is about 13 months (about 393 days, including screening, treatment and follow‑up).
Throughout the duration of the study, participants are required not to smoke and limit their alcohol consumption.
At visits, we undertake health checks and procedures, which can include:
You will be given the investigational medication or placebo via IV infusion. About 75% participants will receive the study drug, and 25% will receive a placebo. A placebo looks like the investigational medicine but contains no active medication. There are three doses given every 2 weeks.
Study Aim
The main purpose is to learn about the study drug and evaluate its safety, tolerability and how the body processes it (pharmacokinetics) in people with eczema. The study also examines eczema severity scores, itch, sleep, and quality‑of‑life measures.
Reason to participate
Your involvement may help advance scientific knowledge and could contribute to developing a future treatment option for eczema - particularly approaches that aim to reduce both inflammation and itch. Other reasons to participate include:
About the investigational medication
The investigational medication is a biologic - a type of drug made from living cells. It’s designed as a “double blocker” that targets two pathways central to eczema:
By blocking both at once, the aim is to reduce skin inflammation and itching - the two main symptoms of eczema.
** All PCRN studies undergo rigorous review processes and are approved by ethics committees and Medsafe.
Apply now
Fill out your details, and our team will be in touch to discuss your potential involvement in this study and answer any questions you may have.
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