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Treatment of Mild to Moderate Joint Pain in Patients With Chronic Plaque Psoriasis Receiving Efalizumab

CompletedPhase 4NCT00510536
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

Brief summary (from the registry)

The purpose of this study is to evaluate tolerability and effectiveness of conventional treatment for mild to moderate arthritic or arthralgic symptoms while subjects are being treated with efalizumab for psoriasis.

Study details

Official title
A Phase 4 Study to Assess the Practical Management of Mild to Moderate Arthritic or Arthralgic Events in Patients With Chronic Plaque Psoriasis Receiving Efalizumab
Sponsor
Probity Medical Research
Start date
2007-07
Primary completion
2008-10
Sex
All
Age range
from 18 Years
Results posted
No results posted in this snapshot
Countries
Canada
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Females cannot become pregnant while participating in study. * Have a history of plaque psoriasis for at least 6 months. * Receiving or about to receive efalizumab for the treatment of chronic plaque psoriasis. * Have mild to moderate arthritis or arthralgia occurring while on treatment with efalizumab or untreated mild to moderate arthritis or arthralgia present at the time of initiating treatment with efalizumab. Exclusion Criteria: * Previous systemic treatment with biologics other than efalizumab, within 3 months. * Treatment with any systemic corticosteroids or intra-articular corticosteroid injection, cyclosporine or methotrexate within 28 days. * Any previous treatment with chlorambucil or cyclophosphamide. * Have active tuberculosis or are currently receiving treatment or prophylactic therapy for tuberculosis. * Have other serious disorders; such as, congestive heart failure, prior or current history of blood dyscrasia, or central nervous system demyelinating disorders. * Has a sensitivity, intolerance, or history of gastrointestinal bleeding associated with diclofenac, indomethacin, and/or ibuprofen.

Canadian sites (1)

FacilityCityProvince
K. Papp Clinical Research Inc.WaterlooOntario

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT00510536