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Recruiting NCT06382051

NCT06382051 Modifying PEST for Psoriatic Arthritis Screening

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Clinical Trial Summary
NCT ID NCT06382051
Status Recruiting
Phase —
Sponsor Novartis Pharmaceuticals
Condition Plaque Psoriasis
Study Type INTERVENTIONAL
Enrollment 502 participants
Start Date 2025-01-23
Primary Completion 2026-12-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
PEST Screening group

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 502 participants in total. It began in 2025-01-23 with a primary completion date of 2026-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The purpose of this study is to assess the impact of adding two questions and pictures to the validated PEST on the potential diagnosis of PsA in participants with moderate-to-severe plaque PsO in Canada.

Eligibility Criteria

Key inclusion criteria: 1. Moderate-to-severe plaque PsO patients who are candidates for bDMARDs, according to physician's clinical judgement at the time of patient enrollment. 2. Adult patients at the time of informed consent signature 3. Patients able to understand and willing to comply with protocol requirements, instructions, and restrictions 4. Residents of Canada Key exclusion criteria: 1. Patients who have previously screened positive for PsA through PEST. 2. Patients who have been diagnosed with PsA. 3. Patients who have been diagnosed with inflammatory arthritis unrelated to PsA (rheumatoid arthritis, reactive arthritis, enteropathic arthritis, axial spondyloarthritis) 4. Patients treated with a bDMARD for moderate-to-severe plaque PsO or any other medical condition within the last 6 months prior to patient enrollment.

Contact & Investigator

Central Contact

Novartis Pharmaceuticals

✉ novartis.email@novartis.com

📞 +41613241111

Principal Investigator

Novartis Pharmaceuticals

STUDY DIRECTOR

Novartis Pharmaceuticals

Frequently Asked Questions

Who can join the NCT06382051 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Plaque Psoriasis. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06382051 currently recruiting?

Yes, NCT06382051 is actively recruiting participants. Contact the research team at novartis.email@novartis.com for enrollment information.

Where is the NCT06382051 trial being conducted?

This trial is being conducted at Calgary, Canada, Edmonton, Canada, Edmonton, Canada, Kelowna, Canada and 11 additional locations.

Who is sponsoring the NCT06382051 clinical trial?

NCT06382051 is sponsored by Novartis Pharmaceuticals. The principal investigator is Novartis Pharmaceuticals at Novartis Pharmaceuticals. The trial plans to enroll 502 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology