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CompletedNCT07386717UVIPWPUpdated Feb 4, 2026

Upadacitinib Versus IL-17 Inhibitors in Patients With Psoriatic Arthritis

An observational study in Psoriatic Arthritis, Upadacitinib and Interleukin-17 Inhibitors, sponsored by Peking University First Hospital. Completed at 1 site in China. Per ClinicalTrials.gov, last updated 2026-02-04.

Sponsored by Peking University First Hospital · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
70
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Psoriatic Arthritis
  • Upadacitinib
  • Interleukin-17 Inhibitors

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Keywords

  • Interleukin-17 Inhibitors
  • Upadacitinib
  • Psoriatic Arthritis
03

In context

Arthritis, Psoriatic

579 studies on the registry are indexed under Arthritis, Psoriatic; 132 are open to participants now.

This study's enrollment of 70 is below the median of 300 across 235 observational studies indexed under Arthritis, Psoriatic.

Browse Arthritis, Psoriatic studies →

Lead sponsor

Peking University First Hospital is the lead sponsor of 378 studies on the registry; 178 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Diagnosis of psoriatic arthritis according to established classification criteria

Inclusion criteria

  • Age ≥ 18 years
  • Diagnosis of psoriatic arthritis according to established classification criteria
  • Treatment with upadacitinib or an interleukin-17 inhibitor at baseline
  • Availability of baseline and follow-up clinical data over 24 weeks

Exclusion criteria

Exclusion Criteria:

  • Diagnosis of other inflammatory arthritides
  • History of malignancy or severe uncontrolled infection
  • Incomplete clinical data preventing outcome assessment
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
70 participants (actual)
Patient registry
No

Groups and cohorts

  • Cohort 1: Upadacitinib-Treated PsA Patients

    Adult patients with psoriatic arthritis receiving upadacitinib as part of routine clinical care and followed for 24 weeks.

  • Cohort 2: IL-17 Inhibitor-Treated PsA Patients

    Adult patients with psoriatic arthritis receiving interleukin-17 inhibitors (e.g., secukinumab or ixekizumab) as part of routine clinical care and followed for 24 weeks.

06

What researchers measure

Primary outcomes

  1. Clinical effectiveness of treatment

    Changes in joint and skin disease activity assessed using validated clinical measures during the 24-week follow-up period.

    Time frame: Baseline to Week 24

07

Study locations

1 site
  • Peking University First Hospital
    Beijing, China
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 4, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07386717
Lead sponsor
Peking University First Hospital
Responsible party
Sponsor
First posted
Feb 4, 2026
Start date
Jan 1, 2024
Primary completion
Dec 31, 2025
Completion
Dec 31, 2025
Last update
Feb 4, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

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