Phase 1 Psoriatic Arthritis Trial, Recruiting
Who may be able to join
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:
General requirements (all participants):
- Adults between 18 and 75 years old
- Having a body weight of at least 45 kg (about 99 lbs) and a body mass index (a height-to-weight measure) between 18 and 40
- Using reliable contraception if able to become pregnant, or having a negative pregnancy test before joining
For Rheumatoid Arthritis (RA):
- Having a confirmed moderate to severe RA diagnosis for at least 3 months, with at least 6 swollen joints, at least 6 tender joints, certain proteins in the blood linked to RA, and elevated inflammation markers
- Having tried at least one standard RA medication that did not work well enough, caused side effects, or stopped working — but not having failed three or more of the advanced RA medications
For Psoriatic Arthritis (PsA):
- Having a confirmed PsA diagnosis for at least 3 months, with at least one active psoriasis skin patch and more than 3 swollen and 3 tender joints
- Having tried standard anti-inflammatory or disease-modifying medications, or being unable to tolerate them
- Having tried no more than one prior TNF-blocker medication
For Psoriasis (PsO):
- Having a confirmed moderate to severe plaque psoriasis diagnosis for at least 6 months, affecting more than 10% of the body surface, with specific severity scores above set thresholds
- Not having had a major flare-up of psoriasis in the past 12 weeks
- Having tried no more than two prior advanced (biologic) psoriasis medications that did not work
For Cutaneous Lupus Erythematosus (CLE — a skin form of lupus):
- Having a confirmed skin lupus diagnosis (proven by a skin biopsy) for at least 6 months, with active skin symptoms above a certain severity score
- Having tried antimalarial treatment (a common lupus medication) for at least 6 months without enough improvement
For Atopic Dermatitis (AD — a type of eczema):
- Having a confirmed eczema diagnosis for at least 12 months, affecting more than 10% of the body surface, with severity scores above set thresholds and significant itch
- Having tried topical (skin-applied) treatments for at least 4 weeks without enough improvement, or having had side effects from them, or having tried and failed other systemic treatments within the past 6 months
Who may not be able to join:
General exclusions (all participants):
- Having previously received certain immune system treatments, including checkpoint inhibitors, cell therapies, or B-cell or immune-depleting therapies (confirm with trial site)
- Having taken certain immune-suppressing medications (azathioprine, cyclosporine, mycophenolate mofetil, or tacrolimus) within the past 4 weeks
- Being unwilling or unable to stop taking any medications that are not allowed during the trial
- Currently having a significantly weakened immune system
- Currently having an infection or having a history of serious infections
- Having had any history of cancer, with some possible exceptions (confirm with trial site)
For CLE specifically:
- Having active kidney inflammation related to lupus, or having moderate-to-severe kidney disease
- Having active lupus affecting the brain or nervous system
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.
Contact this trial
Principal Investigator: Jennifer Martin, MD, Novatrials
Phone: 1800 244 475
Australian sites
+61 (02) 4089 3746
+61 (07) 5456 3872
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.
Trial details
Where this trial is recruiting
2 site(s) in Australia. Confirm current status and contact details directly with the trial site.
Primary endpoints
Incidence of treatment-emergent adverse events (TEAEs); Incidence of serious adverse events (SAEs)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.