CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 30 enrolled
Drug / intervention
Tocilizumab + Glucocorticoids (GCs) +1 moredrug
Likely dose
Tocilizumab + Glucocorticoids (GCs) 8mg/kgfrom 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/NCT01450137
NCT01450137Phase 2Completed

A Phase II, Randomized, Double-blind, Placebo Controlled Study of Tocilizumab in Patients With Giant Cell Arteritis

Insel Gruppe AG, University Hospital Bern·interventional·Posted Oct 12, 2011·Updated Feb 12, 2019

In Brief

A Phase 2 clinical trial evaluating Tocilizumab + Glucocorticoids (GCs) and Placebo + Glucocorticoids (GCs) for Giant Cell Arteritis. Completed, enrolled 30 participants across 1 site.

Detailed Summary

Giant-cell arteritis (GCA) is an immune-mediated disease that mostly affects people older than 50 years of age. Glucocorticoid (GC) treatment dramatically alters the symptoms and course of GCA, reducing the likelihood of vascular complications that could lead e.g. to blindness. However, relapses usually occur when GC dosages are tapered, resulting in frequent re-treatment with high cumulative dosages of GC over time with substantial toxicity and morbidity (e.g. diabetes mellitus, infections, enhanced cardiovascular risk, osteoporotic fractures, cataracts). Therefore, novel therapies are needed that effectively reduce the dose and duration of GC treatment and provide more durable remissions of GCA. Tocilizumab (TCZ) is a humanized monoclonal antibody directed against the human interleukin-6 receptor (IL-6R). Elevated tissue and serum levels of IL-6 have been implicated in giant cell arteritis. Inhibition of IL-6 and/or its receptor therefore represents a new and novel approach for the treatment of RA. The primary endpoint is the proportion of patients that have achieved complete remission of disease after treatment with TCZ compared to treatment with placebo at week 12. All patients will receive glucocorticoids in a standardized form.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesSwitzerland

Timeline

Phase 2CompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedOct 12, 2011
Enrollment StartSep 1, 2011
Primary CompletionDec 1, 2014
Study CompletionSep 1, 2015
TodayJul 2, 2026
Enrollment to primary: 3.3 yearsPosted 14.7 years ago

Interventions

Tocilizumab + Glucocorticoids (GCs)drug

Tocilizumab 8mg/kg every 4 weeks until week 52.

Placebo + Glucocorticoids (GCs)drug

Placebo every 4 weeks until week 52.