Phase 1 Psoriatic Arthritis Trial, Recruiting NCT07455578 Sponsor: Seismic Therapeutic AU Pty Ltd Condition: Psoriatic Arthritis
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Phase 1 Psoriatic Arthritis Trial, Recruiting

NCT07455578
Recruiting Phase 1 🇦🇺 Australian site

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.

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 28 July 2026
Phase 1: approximately ~10% 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.

Contact this trial

Principal Investigator: Jennifer Martin, MD, Novatrials

Phone: 1800 244 475

Australian sites

Novatrials, Charlestown, New South Wales
+61 (02) 4089 3746
University of the Sunshine Coast Clinical Trials, Birtinya, Birtinya, Queensland
+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

Status
Recruiting
Phase
Phase 1
Sponsor
Seismic Therapeutic AU Pty Ltd
Registry
ClinicalTrials.gov
Start date
1 June 2026
Est. completion
1 September 2027

Where this trial is recruiting

🇦🇺 Australia

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?

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.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

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.

View original record on ClinicalTrials.gov