Phase 1 Psoriatic Arthritis Trial, Recruiting NCT06751238 Sponsor: Novartis Pharmaceuticals Condition: Psoriatic Arthritis
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Phase 1 Psoriatic Arthritis Trial, Recruiting

NCT06751238
Recruiting Phase 1

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:

  • A parent or legal guardian must provide written consent before any study activities begin, and the child must also give their agreement if old enough to do so under local law.
  • Children and teenagers aged 2 years old up to (but not including) 18 years old at the time of screening.
  • People who have a confirmed diagnosis of Juvenile Psoriatic Arthritis (JPsA), diagnosed at least 6 months before screening, based on recognised international classification criteria.
  • People whose JPsA is currently active, meaning at least 3 joints are swollen, or tender and have limited movement.
  • People who have tried at least one anti-inflammatory painkiller (such as ibuprofen or naproxen) for at least 1 month without enough improvement, or who could not tolerate it.
  • People who have tried at least one disease-modifying arthritis medication for at least 2 months without enough improvement, or who could not tolerate it.
  • People who are taking certain stable-dose medications alongside the trial treatment may still be eligible, including: methotrexate (at a set maximum dose for at least 4 weeks before the study start), low-dose oral steroids (at or below a specified threshold for at least 7 days before the study start), or a single anti-inflammatory painkiller (stable for at least 1 week before the study start).

Who may not be able to join:

  • Children who weigh less than 10 kg at the time of screening.
  • People who have taken another experimental drug within 4 weeks or 5 half-lives before the study start (whichever is longer).
  • People who have had an allergic reaction to the study drug, its ingredients, or to similar types of medications.
  • People who have active inflammatory bowel disease or active eye inflammation (uveitis) at the time of screening or the study start.
  • People whose joint disease meets the diagnostic criteria for a different category of juvenile idiopathic arthritis (other than JPsA).
  • People who are taking medications that are not permitted under the trial rules.
  • People who are taking any non-biologic disease-modifying arthritis medication other than methotrexate at the time of screening.
  • People who have a medical or psychiatric condition that, in the treating doctor's opinion, would make it difficult to follow the study requirements.

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

Phone: 1-888-669-6682

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
Registry
ClinicalTrials.gov
Start date
24 September 2025
Est. completion
30 November 2032

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Maximum concentration on Day 1; Maximum concentration at steady-state (Cmax, ss); Minimum concentration at steady-state (Cmin, ss); Area under the concentration-time curve at steady-state (AUCtau, ss); Average concentration at steady-state (Cavg,ss)

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