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A Study to Evaluate the Efficacy, Safety and Tolerability of BMS-986368 in Participants With Multiple Sclerosis Spasticity

Multiple Sclerosis Spasticity

The purpose of this study is to evaluate the efficacy, safety, and tolerability of BMS-986368 in participants with Multiple Sclerosis Spasticity

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Conditions de participation

  • Sexe:

    ALL
  • Âges admissibles:

    18 to 70

Critères de participation

Inclusion Criteria

* Participants must have a multiple sclerosis (MS) diagnosis.
* Participants must have a history of spasticity due to MS for at least 6 months prior to Visit 1.
* Participants must have a Modified Ashworth Scale (mAS) score ≥2 in each of 2 muscle groups (at least one muscle group in the leg, excluding ankle plantar flexors) at Visit 1.
* Participants must have an Expanded Disability Status Scale (EDSS) score 3.0-6.5 at Visit 1.

Exclusion Criteria

* Participants must not have any concomitant disease or disorder that has symptoms of spasticity or that may influence the participant's level of spasticity.
* Participants must not have an acute MS exacerbation/relapse requiring treatment or alteration in disease modifying drug dose within 3 months of Visit 1 or Visit 2.
* Participants must not have a history of any substance abuse disorder as defined in Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) Diagnostic Criteria for Drug and Alcohol Abuse.
* Participants must not be currently taking a medication for spasticity that cannot be discontinued and washed out by Visit 2.
* Participants must not have used FAAH/MAGL inhibitor medication or any cannabinoid-related products (including cannabis, cannabidiol (CBD), or tetrahydrocannabinol (THC)) within 30 days prior to Visit 1.
* Other protocol-defined Inclusion/Exclusion criteria apply.

Lieu de l'étude

Local Institution - 0028
Local Institution - 0028
Toronto, Ontario
Canada

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Primary Contact

Site 0028

Local Institution - 0012
Local Institution - 0012
Ottawa, Ontario
Canada

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Primary Contact

Site 0012

Local Institution - 0024
Local Institution - 0024
London, Ontario
Canada

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Primary Contact

Site 0024

Local Institution - 0029
Local Institution - 0029
Montreal, Quebec
Canada

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Primary Contact

Site 0029

Local Institution - 0013
Local Institution - 0013
Edmonton, Alberta
Canada

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Primary Contact

Site 0013

Centre de Recherche Saint-Louis
Centre de Recherche Saint-Louis
Lévis, Quebec
Canada

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Primary Contact

Donald Rivest, Site 0014

418-780-3501x2703
Montreal Neurological Institute and Hospital
Montreal Neurological Institute and Hospital
Montreal, Quebec
Canada

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Primary Contact

Adil Harroud, Site 0029

(514) 396-2950
The Ottawa Hospital - General Campus
The Ottawa Hospital - General Campus
Ottawa, Ontario
Canada

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Primary Contact

Mark Freedman, Site 0012

613-737-8104
Étude parrainée par
Celgene
Participants recherchés
Plus d'informations
ID de l'étude: NCT06782490