Lymphocyte and Cytokine Disturbances in Polymyalgia Rheumatica

NCT02888496 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 40

Last updated 2016-09-05

No results posted yet for this study

Summary

Pathophysiology of polymyalgia rheumatica (PMR) is ill defined. This study aims at characterizing immunological abnormalities in PMR patients, and to assess the effects of tocilizumab therapy on this abnormalities.

Conditions

  • Polymyalgia Rheumatica

Interventions

DRUG

tocilizumab

3 monthly IV infusions in PMR patients

Sponsors & Collaborators

  • University Hospital, Brest

    lead OTHER

Principal Investigators

  • Divi Cornec · CHRU de Brest

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-01-31
Primary Completion
2015-06-30
Completion
2015-06-30

Countries

  • France

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02888496 on ClinicalTrials.gov