Clinical Trials Directory

Trials / Completed

CompletedNCT07386717

Upadacitinib Versus IL-17 Inhibitors in Patients With Psoriatic Arthritis

Upadacitinib Versus IL-17 Inhibitors in Patients With Psoriatic Arthritis: A Cohort Study

Status
Completed
Phase
Study type
Observational
Enrollment
70 (actual)
Sponsor
Peking University First Hospital · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Psoriatic arthritis (PsA) is a chronic inflammatory disease with heterogeneous musculoskeletal and dermatologic manifestations, leading to significant functional impairment and reduced quality of life. Although targeted therapies such as Janus kinase inhibitors and interleukin-17 inhibitors have demonstrated efficacy in randomized controlled trials, real-world comparative evidence between these treatment strategies remains limited. This observational cohort study aims to compare the real-world effectiveness and safety of upadacitinib and interleukin-17 inhibitors in patients with PsA over a 24-week follow-up period. By evaluating clinical outcomes under routine clinical practice conditions, this study seeks to provide evidence to support individualized treatment selection in PsA management.

Detailed description

This is a real-world, observational cohort study conducted at Peking University First Hospital. Adult patients diagnosed with psoriatic arthritis will be enrolled and followed for 24 weeks in routine clinical practice. Participants will be categorized into two cohorts based on treatment exposure at baseline: patients receiving upadacitinib and patients receiving interleukin-17 inhibitors. Treatment decisions are made by treating physicians according to standard clinical practice and are not influenced by the study protocol. Clinical assessments will be performed at baseline and during routine follow-up visits within the 24-week observation period. Effectiveness outcomes will be evaluated across musculoskeletal and dermatologic domains, and safety outcomes will be monitored throughout follow-up. This study does not involve experimental interventions.

Conditions

Timeline

Start date
2024-01-01
Primary completion
2025-12-31
Completion
2025-12-31
First posted
2026-02-04
Last updated
2026-02-04

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07386717. Inclusion in this directory is not an endorsement.