Journal article icon

Journal article

Efficacy and Safety of Inebilizumab in IgG4-Related Disease: Protocol for a Randomized Controlled Trial

Abstract:
INTRODUCTION: B cells thought to be involved in IgG4-RD pathogenesis. We describe the first international, prospective, double-blind, placebo-controlled trial to evaluate the safety and efficacy of B-cell depletion for flare prevention in IgG4-RD (MITIGATE). METHODS: The study was designed by an international panel of physicians with expertise in IgG4-RD. Critical trial design decisions included the selection of participants, definition of clinically meaningful primary and secondary endpoints, accommodation of standard of care, and development of flare diagnostic criteria. The study is approved for conduct in 22 countries. PLANNED OUTCOMES: The primary efficacy endpoint is time from randomization to the occurrence of the first centrally adjudicated and investigator-treated disease flare during the 1-year randomized controlled period. A set of novel, organ-specific flare diagnostic criteria were developed specifically for this trial, incorporating symptoms and signs, laboratory findings, imaging study results, and pathology data. MITIGATE aims to accrue 39 flares for the primary endpoint, which provides sufficient power to detect a relative risk reduction of 65% in the inebilizumab group. It is anticipated that enrollment of 160 participants will achieve this goal. Additional endpoints include safety, annualized flare rate, flare-free complete remission, quality-of-life measures, and cumulative glucocorticoid use. MITIGATE represents the first randomized, double-blind, placebo-controlled trial of any treatment strategy conducted in IgG4-RD. Data from this study will provide insights into the natural history and pathophysiology of IgG4-RD and the efficacy and safety of B-cell depletion as a therapeutic avenue. TRIAL REGISTRATION: NCT04540497.
Publication status:
Published
Peer review status:
Peer reviewed

Actions

Access Document

Files:
Publisher copy:
10.1007/s40744-023-00593-7

Authors

More by this author
Institution:
University of Oxford
Role:
Author
ORCID:
0000-0001-9644-8392
More by this author
Role:
Author
ORCID:
0000-0001-8365-8497
More by this author
Role:
Author
ORCID:
0000-0001-7808-9867
More by this author
Role:
Author
ORCID:
0000-0002-9192-4270


More from this funder
Funder identifier:
10.13039/100019637


Publisher:
Springer
Journal:
Rheumatology and Therapy More from this journal
Volume:
10
Issue:
6
Pages:
1795-1808
Publication date:
2023-10-04
DOI:
EISSN:
2198-6584
ISSN:
2198-6576


Language:
English
Keywords:
Pubs id:
1546612
Local pid:
pubs:1546612
Source identifiers:
W4387327114
Deposit date:
2026-05-17
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

Terms of use


Views and Downloads






If you are the owner of this record, you can report an update to it here: Report update to this record

TO TOP