Safety and acceptability of clozapine and risperidone in progressive multiple sclerosis: a phase I, randomised, blinded, placebo-controlled trial.

multiple sclerosis

Journal

BMJ neurology open
ISSN: 2632-6140
Titre abrégé: BMJ Neurol Open
Pays: England
ID NLM: 101775450

Informations de publication

Date de publication:
2020
Historique:
received: 23 03 2020
revised: 28 05 2020
accepted: 01 06 2020
entrez: 8 3 2021
pubmed: 9 3 2021
medline: 9 3 2021
Statut: epublish

Résumé

Because clozapine and risperidone have been shown to reduce neuroinflammation in humans and mice, the Clozapine and Risperidone in Progressive Multiple Sclerosis (CRISP) trial was conducted to determine whether clozapine and risperidone are suitable for progressive multiple sclerosis (pMS). The CRISP trial (ACTRN12616000178448) was a blinded, randomised, placebo-controlled trial with three parallel arms (n=12/arm). Participants with pMS were randomised to clozapine (100-150 mg/day), risperidone (2.0-3.5 mg/day) or placebo for 6 months. The primary outcome measures were safety (adverse events (AEs)/serious adverse events (SAE)) and acceptability (Treatment Satisfaction Questionnaire for Medication-9). An interim analysis (n=9) revealed significant differences in the time-on-trial between treatment groups and placebo (p=0.030 and 0.025, clozapine and risperidone, respectively) with all participants receiving clozapine being withdrawn during the titration period (mean dose=35±15 mg/day). Participants receiving clozapine or risperidone reported a significantly higher rate of AEs than placebo (p=0.00001) but not SAEs. Specifically, low doses of clozapine appeared to cause an acute and dose-related intoxicant effect in patients with pMS who had fairly severe chronic spastic ataxic gait and worsening over all mobility, which resolved on drug cessation. The CRISP trial results suggest that patients with pMS may experience increased sensitivity to clozapine and risperidone and indicate that the dose and/or titration schedule developed for schizophrenia may not be suitable for pMS. While these findings do not negate the potential of these drugs to reduce multiple sclerosis-associated neuroinflammation, they highlight the need for further research to understand the pharmacodynamic profile and effect of clozapine and risperidone in patients with pMS. ACTRN12616000178448.

Identifiants

pubmed: 33681788
doi: 10.1136/bmjno-2020-000060
pii: bmjno-2020-000060
pmc: PMC7903182
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e000060

Informations de copyright

© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: ACL and BC have a patent for the use of clozapine and risperidone during MS. ACL is a founding scientist and shareholder in ReKover Therapeutics, which has no relationship to the Clozapine and Risperidone in Progressive Multiple Sclerosis study. In addition, BC has a patent PCT/US2011/042244 issued.

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Auteurs

Anne C La Flamme (AC)

School of Biological Sciences, Victoria University of Wellington, Wellington, New Zealand.
Malaghan Institute of Medical Research, Wellington, New Zealand.

David Abernethy (D)

Neurology, Wellington Regional Hospital, Wellington, New Zealand.

Dalice Sim (D)

Biostatistical Consulting Group, University of Otago, Wellington, New Zealand.

Liz Goode (L)

Neurology, Wellington Regional Hospital, Wellington, New Zealand.

Michelle Lockhart (M)

Pharmaceuticol Ltd, Auckland, New Zealand.

David Bourke (D)

Neurology, Wellington Regional Hospital, Wellington, New Zealand.

Imogen Milner (I)

Neurology, Wellington Regional Hospital, Wellington, New Zealand.

Toni-Marie Garrill (TM)

Neurology, Wellington Regional Hospital, Wellington, New Zealand.

Purwa Joshi (P)

Neurology, Wellington Regional Hospital, Wellington, New Zealand.

Eloise Watson (E)

Neurology, Wellington Regional Hospital, Wellington, New Zealand.

Duncan Smyth (D)

Neurology, Wellington Regional Hospital, Wellington, New Zealand.

Sean Lance (S)

Hutt Valley District Health Board, Lower Hutt, New Zealand.

Bronwen Connor (B)

Department of Pharmacology and Clinical Pharmacology, Centre for Brain Research, Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.

Classifications MeSH