Printed from Voxsanity (voxsanity.com.au) — NCT06380907 — Data sourced from ClinicalTrials.gov. Verify directly with the trial site before attending. Not medical advice.
AI generated eligibility summary.
Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source.
How we use AI
Who might be able to join this trial:
Adults aged 18 or older
People who are willing and able to sign a consent form before any study activities begin, and who are able to follow all study procedures
People who have been diagnosed with plaque psoriasis for at least 6 months, whose condition is currently suitable for treatment with creams or ointments applied to the skin, and whose psoriasis meets specific severity and affected skin area measurements at the screening and baseline visits (the affected area must be between 3% and 15% of the body, not counting the head, and the investigator must rate the severity at a certain level — confirm with trial site)
People who agree to avoid prolonged sun exposure (such as sunbathing) during the study, and who agree not to use tanning beds or LED light devices
Who may not be able to join:
People whose psoriasis is mainly a type other than plaque psoriasis — for example, psoriatic arthritis, pustular, erythrodermic, guttate, or psoriasis affecting the palms, soles, scalp, or nails — or whose condition requires treatment beyond skin-applied products
People with a serious medical or psychiatric condition, or significant abnormal lab results, that the investigator determines would make study participation unsafe or unsuitable
People with known or suspected severe kidney or liver problems
People with a history of severe depression or thoughts or actions related to suicide within the 2 years before screening
People who test positive at screening for HIV, Hepatitis B, or Hepatitis C
People with active tuberculosis (TB), or latent TB that has not been treated according to local medical guidelines
People with a current or past history of inflammatory bowel disease (such as ulcerative colitis or Crohn's disease), or who show signs of this condition at screening that the investigator considers to pose an unacceptable risk
People with a history of a serious allergic reaction (such as anaphylaxis) to a type of medication known as IL-17 antibodies, or to any human or humanised biological medicines
People with a history of cancer, unless they have been considered fully treated with no signs of return for at least 3 years before the study begins
People with a history of long-term alcohol or drug misuse within 6 months before the study begins, as determined by the investigator
People who have previously received the study drug ZL-1102
People who have received a live vaccine within 6 weeks before the first dose of the study drug
People who are pregnant, planning to become pregnant during the study, or who are currently breastfeeding
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 16 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.
Zai Lab Site 5013, Phillip, Australian Capital Territory
Zai Lab Site 5021, Kogarah, New South Wales
Zai Lab Site 5016, Kotara, New South Wales
Zai Lab Site 5020, Birtinya, Queensland
Zai Lab Site 5019, Coorparoo, Queensland
Zai Lab Site 5017, Woolloongabba, Queensland
Zai Lab Site 5014, Carlton, Victoria
Zai Lab Site 5015, Melbourne, Victoria
Zai Lab Site 5002, Melbourne E., Victoria
Zai Lab Site 5018, Parkville, Victoria
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Voxsanity
Clinical trials and treatments, explained plainly · voxsanity.com.au
Date:
To: My Doctor
Re: Clinical trial enquiry
I am writing to enquire about the following clinical trial which may be relevant to my care:
Trial: NCT06380907
Sponsor: Zai Lab (Hong Kong), Ltd.
Phase: Phase 2
Status: Recruiting
Condition: Psoriasis
Trial contact: 857-971-3465
More information: https://clinicaltrials.gov/study/NCT06380907
Eligibility summary (AI generated)
Written by an AI model from ClinicalTrials.gov eligibility criteria and checked on a sample basis. Please confirm against the original criteria.
Who might be able to join this trial:
Adults aged 18 or older
People who are willing and able to sign a consent form before any study activities begin, and who are able to follow all study procedures
People who have been diagnosed with plaque psoriasis for at least 6 months, whose condition is currently suitable for treatment with creams or ointments applied to the skin, and whose psoriasis meets specific severity and affected skin area measurements at the screening and baseline visits (the affected area must be between 3% and 15% of the body, not counting the head, and the investigator must rate the severity at a certain level — confirm with trial site)
People who agree to avoid prolonged sun exposure (such as sunbathing) during the study, and who agree not to use tanning beds or LED light devices
Who may not be able to join:
People whose psoriasis is mainly a type other than plaque psoriasis — for example, psoriatic arthritis, pustular, erythrodermic, guttate, or psoriasis affecting the palms, soles, scalp, or nails — or whose condition requires treatment beyond skin-applied products
People with a serious medical or psychiatric condition, or significant abnormal lab results, that the investigator determines would make study participation unsafe or unsuitable
People with known or suspected severe kidney or liver problems
People with a history of severe depression or thoughts or actions related to suicide within the 2 years before screening
People who test positive at screening for HIV, Hepatitis B, or Hepatitis C
People with active tuberculosis (TB), or latent TB that has not been treated according to local medical guidelines
People with a current or past history of inflammatory bowel disease (such as ulcerative colitis or Crohn's disease), or who show signs of this condition at screening that the investigator considers to pose an unacceptable risk
People with a history of a serious allergic reaction (such as anaphylaxis) to a type of medication known as IL-17 antibodies, or to any human or humanised biological medicines
People with a history of cancer, unless they have been considered fully treated with no signs of return for at least 3 years before the study begins
People with a history of long-term alcohol or drug misuse within 6 months before the study begins, as determined by the investigator
People who have previously received the study drug ZL-1102
People who have received a live vaccine within 6 weeks before the first dose of the study drug
People who are pregnant, planning to become pregnant during the study, or who are currently breastfeeding
Important: Always verify eligibility with the trial site directly before applying.
Access in Australia: A treatment being studied in a clinical trial is generally not yet listed on the PBS. Where a medicine is not approved or not available through a trial, the TGA Special Access Scheme may allow a doctor to access unapproved therapeutic goods for individual patients. See voxsanity.com.au/sas-navigator/ for a plain English explainer.
This information was sourced from ClinicalTrials.gov via Voxsanity (data last synced 16 July 2026). It is not medical advice. Please verify the trial's current status directly with the trial site before acting.
Trial details
Status
Recruiting
Phase
Phase 2
Sponsor
Zai Lab (Hong Kong), Ltd.
Registry
ClinicalTrials.gov
Start date
22 May 2024
Est. completion
28 February 2026
Where this trial is recruiting
🇦🇺 Australia
10 site(s) in Australia. Confirm current status and contact details directly with the trial site.
Primary endpoints
Efficacy of different doses of ZL-1102 compared to Vehicle at Week 16.
Can't join this trial?
Expanded access pathways
If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.
Data last synced from ClinicalTrials.gov: 16 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.
Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.