Efficacy And Safety Of Tofacitinib In Chinese Subjects With Active Psoriatic Arthritis

  • STATUS
    Recruiting
  • End date
    May 15, 2021
  • participants needed
    195
  • sponsor
    Pfizer
Updated on 11 November 2020
Investigator
Pfizer CT.gov Call Center
Primary Contact
Department of Rheumatology, Northern Jiangsu People's Hospital (2.0 mi away) Contact
+43 other location
psoriasis
tofacitinib
arthritis
rheumatic diseases
DMARD
plaque psoriasis

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.

Details
Treatment Placebo, tofacitinib
Clinical Study IdentifierNCT03486457
SponsorPfizer
Last Modified on11 November 2020

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Eligibility

Yes No Not Sure

Inclusion Criteria

Is your age greater than or equal to 18 yrs?
Gender: Male or Female
Do you have any of these conditions: Arthritis and Arthritic Pain or Arthritis or Psoriasis and Psoriatic Disorders or Psoriasis or PSORIATIC ARTHRITIS or Arthritis and Arthritic Pain (Pe...?
Do you have any of these conditions: Arthritis or Arthritis and Arthritic Pain (Pediatric) or PSORIATIC ARTHRITIS or Psoriasis and Psoriatic Disorders or Arthritis and Arthritic Pain or P...?
Chinese patients
Active arthritis at screening/baseline as indicated by >/= 3 tender/painful and 3 swollen joints
Active plaque psoriasis at screening
Inadequate response to at least one conventional synthetic DMARD

Exclusion Criteria

Non-plaque forms of psoriasis (with exception of nail psoriasis)
History of autoimmune rheumatic disease other than PsA; also prior history of or current, rheumatic inflammatory disease other than PsA
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