A Study to Assess the Change in Disease State in Adult Participants Being Treated With Oral Upadacitinib Tablets in Participants With Oligo- or Poly-artIcular Psoriatic Arthritis (UPJOINT)

AbbVie

Status: Completed

Conditions: Psoriatic Arthritis

Study type: Observational

Funder types: Industry

Identifiers

NCT04758117

P20-483

Details and patient eligibility

About

Psoriatic arthritis (PsA) is a type of arthritis (swelling and stiffness in the joints) that is frequently seen in trial participants who also have the skin condition psoriasis. It is caused by the body's immune system mistakenly attacking healthy joint tissue causing inflammation, joint damage, disability, and a reduced life expectancy. The main objective of this study is to characterize attainment of minimal disease activity (MDA) at week 24 under continuous treatment with upadacitinib in participants with oligo- or polyarticular PsA as part of real-world practice.

Upadacitinib is a drug approved for the treatment of Psoriatic arthritis (PsA) in Germany and Canada. Approximately 380 adult participants with PsA at multiple sites in Germany and Canada.

Participants will receive oral Upadacitinib tablets per current local label, according to local standard of care and international guidelines.

There may be a higher burden for participants in this study compared to standard of care. Participants will attend regular visits per routine clinical practice. The effect of the treatment will be checked by medical assessments, checking for side effects, and by questionnaire.

Enrollment: 394 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Diagnosis of active Psoriatic Arthritis (PsA) upon judgment of the treating physician.
• Swollen joint count (SJC) >= 1 out of 66 joints.
• Decision on the treatment with Upadacitinib was made prior to any decision to approach the participant to participate in this study.

Exclusion criteria

• Cannot be treated with Upadacitinib according to the local Upadacitinib Summary of Product Characteristics (SmPC).
• Prior treatment with Upadacitinib.
• Currently participating in interventional research or within the last 30 days.

Trial design

394 participants in 1 patient group

Participants Receiving Upadacitinib

Description:

Participants receiving Upadacitinib for psoriatic arthritis (PsA).