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Efficacy, safety and tolerability of rozanolixizumab in patients with chronic inflammatory demyelinating polyradiculoneuropathy: A randomised, subject-blind, investigator-blind, placebo-controlled, phase 2a trial and open-label extension study

  • Luis Querol(corresponding author)
    ,
  • Jérôme De Sèze
    ,
  • Tina Dysgaard
    ,
  • Todd Levine
    ,
  • T. Hemanth Rao
    ,
  • Michael Rivner
*Corresponding author for this work
  • Autonomous University of Barcelona
    ,
  • Centro de Investigación Biomédica en Red
    ,
  • CHU Strasbourg
    ,
  • University of Copenhagen
    ,
  • Bob Bove Neuroscience Institute
    ,
  • PA
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Background Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is a peripheral nerve disorder characterised by weakness and sensory loss. We assessed the neonatal Fc receptor inhibitor rozanolixizumab for CIDP management. Methods CIDP01 (NCT03861481) was a randomised, subject-blind, investigator-blind, placebo-controlled, phase 2a study. Adults with definite or probable CIDP receiving subcutaneous or intravenous immunoglobulin maintenance therapy were randomised 1:1 to 12 once-weekly subcutaneous infusions of rozanolixizumab 10 mg/kg or placebo, stratified according to previous immunoglobulin administration route. Investigators administering treatment and assessing efficacy, and patients, were blinded. The primary outcome was a change from baseline (CFB) to day 85 in inflammatory Rasch-built Overall Disability Scale (iRODS) score. Eligible patients who completed CIDP01 entered the open-label extension CIDP04 (NCT04051944). Results In CIDP01, between 26 March 2019 and 31 March 2021, 34 patients were randomised to rozanolixizumab or placebo (17 (50%) each). No significant difference in CFB to day 85 in iRODS centile score was observed between rozanolixizumab (least squares mean 2.0 (SE 3.2)) and placebo (3.4 (2.6); difference -1.5 (90% CI -7.5 to 4.5)). Overall, 14 (82%) patients receiving rozanolixizumab and 13 (76%) receiving placebo experienced a treatment-emergent adverse event during the treatment period. Across CIDP01 and CIDP04, rozanolixizumab was well tolerated over up to 614 days; no clinically meaningful efficacy results were seen. No deaths occurred. Conclusions Rozanolixizumab did not show efficacy in patients with CIDP in this study, although this could be due to a relatively high placebo stability rate. Rozanolixizumab was well tolerated over medium-to-long-term weekly use, with an acceptable safety profile.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 845-854 (10 pages)

Journal (Volume, Issue Number)

Journal of Neurology, Neurosurgery and Psychiatry (Volume 95, Issue 9)

Publication milestones

  • Accepted/In press - 2024
  • Published - 08/16/2024

Publication status

Published - 08/16/2024

ISSN

0022-3050

Publication IDs

  • Scopus: 85193411110
  • PubMed: 38729747

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13
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0.93
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1
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1
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27
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Funding Details

The authors thank the patients and their caregivers, in addition to the investigators and their teams who contributed to this study. Medical writing support was provided by Luke Worley, Niall Harrison and Bryony McNamara of Ogilvy Health and funded by UCB Pharma, in accordance with Good Publication Practice guidelines ( https://www.ismpp.org/gpp-2022 ). Authors were neither paid to participate nor precluded from accessing data from the study. The authors thank Veronica Porkess, PhD, of UCB Pharma for publication and editorial support. This work has been previously presented at the Peripheral Nerve Society 2022 Annual Meeting (poster 67/e-poster 1216).
FunderFunding numbers
UCB
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