Advice

following an abbreviated submission:

ublituximab (Briumvi®) is accepted for restricted use within NHSScotland.

Indication under review: treatment of adult patients with relapsing forms of multiple sclerosis (RMS) with active disease defined by clinical or imaging features.

SMC restriction: treatment of relapsing-remitting multiple sclerosis (RRMS) with active disease defined by clinical or imaging features.

Ublituximab offers an additional treatment choice in the therapeutic class of anti-CD20 monoclonal antibodies.

This advice applies only in the context of approved NHSScotland Patient Access Scheme (PAS) arrangements delivering the cost-effectiveness results upon which the decision was based, or PAS/ list prices that are equivalent or lower.

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Medicine details

Medicine name:
ublituximab (Briumvi)
SMC ID:
SMC2731
Indication:

For the treatment of adult patients with relapsing forms of multiple sclerosis (RMS) with active disease defined by clinical or imaging features.

Pharmaceutical company
Neuraxpharm UK Ltd
BNF chapter
Central nervous system
Submission type
Abbreviated
Status
Restricted
Date advice published
13 January 2025