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Wiley InterScience

European Journal of Neurology

European Journal of Neurology

Volume 14 Issue 3, Pages 290 - 296

Published Online: 23 Feb 2007

Journal compilation © 2010 European Federation of Neurological Societies



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Randomized controlled trial of cannabis-based medicine in spasticity caused by multiple sclerosis
C. Collin a , P. Davies b , I. K. Mutiboko c , S. Ratcliffe d for the Sativex Spasticity in MS Study Group*
  a Department of Neurorehabilitation, Royal Berkshire and Battle NHS Trust, Reading, UK ;   b Department of Neurology, Northampton General Hospital, Northampton, UK ;   c Trial-Link Ltd, Bexhill-on-Sea, UK ; and   d Barts Pain Research Group, Barts and The London NHS Trust, London, UK
Correspondence to Christine Collin, Department of Neurorehabilitation, Royal Berkshire and Battle NHS Trust, London Road Reading, Berkshire RG1 5AN, UK (tel.: 0118 322 5367; fax: 0118 322 6751; e-mail: christine.collin@rbbh-tr.nhs.uk).

  *The Sativex® Spasticity in MS Study Group comprise the following: Dr C. H. Hawkes, Oldchurch Hospital, Romford, UK; Prof. C. Hawkins, University Hospital of North Staffordshire NHS Trust, Stoke-On-Trent, UK; Dr R. Stevens, Amersham General Hospital, Amersham, UK; Dr W. Notcutt, James Paget Hospital, Great Yarmouth, UK; Dr D. Minea, Spitalul de Neuropsihiatrie, Brasov, Romania; Dr C. Zaharia, Spitalul Clinic de Neuropsihiatrie, Craiova, Romania; Dr M. Pereanu, Spitalul Clinic, Judetean Sibiu Sectia, Sibiu, Romania; Dr C. Protosevici, Spitalul Clinic, Bucuresti, Romania; Dr Stephen Wright, Richard Potts, Rebecca McCalla, and Paul Duncombe, GW Pharmaceuticals Plc, Salisbury, UK.

Copyright 2007 EFNS
KEYWORDS
cannabis-based medicine • multiple sclerosis • Sativex • spasticity

ABSTRACT

Symptoms relating to spasticity are common in multiple sclerosis (MS) and can be difficult to treat. We have investigated the efficacy, safety and tolerability of a standardized oromucosal whole plant cannabis-based medicine (CBM) containing Δ-9 tetrahydrocannabinol (THC) and cannabidiol (CBD), upon spasticity in MS. A total of 189 subjects with definite MS and spasticity were randomized to receive daily doses of active preparation (n = 124) or placebo (n = 65) in a double blind study over 6 weeks. The primary endpoint was the change in a daily subject-recorded Numerical Rating Scale of spasticity. Secondary endpoints included a measure of spasticity (Ashworth Score) and a subjective measure of spasm. The primary efficacy analysis on the intention to treat (ITT) population (n = 184) showed the active preparation to be significantly superior (P = 0.048). Secondary efficacy measures were all in favour of active preparation but did not achieve statistical significance. The responder analysis favoured active preparation, 40% of subjects achieved >30% benefit (P = 0.014). Eight withdrawals were attributed to adverse events (AEs); six were on active preparation and two on placebo. We conclude that this CBM may represent a useful new agent for treatment of the symptomatic relief of spasticity in MS.


Received 6 April 2006 Accepted 18 August 2006

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1468-1331.2006.01639.x About DOI

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