CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 204 enrolled
Drug / intervention
Tofacitinib +2 moredrug
Likely dose
Tofacitinib 5 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03486457
NCT03486457Phase 3Completed

A PHASE 3, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY OF THE EFFICACY AND SAFETY OF TOFACITINIB (CP-690,550) IN CHINESE SUBJECTS WITH ACTIVE PSORIATIC ARTHRITIS AND AN INADEQUATE RESPONSE TO AT LEAST ONE CONVENTIONAL SYNTHETIC DMARD

Pfizer·interventional·Posted Apr 3, 2018·Updated Feb 8, 2024

In Brief

A Phase 3 clinical trial evaluating Tofacitinib and Placebo for Psoriatic Arthritis. Completed, enrolled 204 participants across 38 sites.

Detailed Summary

This is a 6 month study investigating the effectiveness and safety of tofacitinib in treating signs and symptoms and improving physical function in Chinese patients with active psoriatic arthritis and had inadequate response to a conventional synthetic disease modifying anti-rheumatic drug. This is a China alone study.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

Phase 3CompletedFinished
20192020202120222023202420252026
First PostedApr 3, 2018
Enrollment StartAug 10, 2018
Primary CompletionApr 28, 2021
TodayJul 2, 2026
Enrollment to primary: 2.7 yearsPosted 8.2 years ago

Interventions

Tofacitinibdrug

tablets, 5 mg BID x 6 months

Placeboother

tablets, to match tofacitinib 5 mg BID x 3 months

Tofacitinibdrug

tablets, 5 mg BID x 3 months