drugset / Trial / NCT04762784

A Prospective Study of Tocilizumab in the Treatment of Idiopathic Retroperitoneal Fibrosis

NCT04762784

Phase 4 Unknown 40 enrolled Peking Union Medical College Hospital
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is a prospective study to investigate the treatment response of Tocilizumab on patients with idiopathic retroperitoneal fibrosis(IRPF). Methods: All the patients fulfilling diagnostic criteria of IRPF would be enrolled. The IRPF patients will accept Tocilizumab or Glucocorticoid monotherapy for 3 months. Endpoints: The primary endpoint is to investigate the response of Tocilizumab on IRPF patients; the secondary endpoints include the decrease of inflammatory markers, side effect.

Timeline

Start
2020-07-01
Primary completion
2023-02-10
Completion
2023-02-10

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Prednisolone Other / unclassified 15 mg
Comparator Prednisone Other / unclassified 15 mg Oral
Subject Tocilizumab Monoclonal antibody 8 mg/kg

Indications

No indication recorded.