Formulary Decisions

Search for the outcome of decisions made by the Formulary Committee

Filter
Select filter(s)
Tocilizumab
Tocilizumab
Routinely available
SMC (982/14)
27/03/2024

Indication

In combination with methotrexate (MTX) for the treatment of moderate to severe active rheumatoid arthritis (RA) in adult patients who have either responded inadequately to, or who were intolerant to previous therapy with one or more disease-modifying anti-rheumatic drugs (DMARDs) or tumour necrosis ...

In combination with methotrexate (MTX) for the treatment of moderate to severe active rheumatoid arthritis (RA) in adult patients who have either responded inadequately to, or who were intolerant to previous therapy with one or more disease-modifying anti-rheumatic drugs (DMARDs) or tumour necrosis factor (TNF) antagonists. In these patients, tocilizumab can be given as monotherapy in case of intolerance to MTX or where continued treatment with MTX is inappropriate. Tocilizumab has been shown to reduce the rate of progression of joint damage as measured by X-ray and to improve physical function when given in combination with methotrexate.

Therapeutic Area

Musculoskeletal and joint diseases

Status Description

Routinely available in line with local or regional guidance

Formulation

162mg solution for injection in pre-filled syringe

Comments

Refer to pathway or local board guidelines for preferred formulation.

Link to Advice

982/14

Advice Published

11/08/2014

SMC Submission Type

Full

SMC Status

Restricted