Extended indication Rheumatoid arthritis (RA), giant lymph node hyperplasia (Castlesman’s disease), polyarticular idioathic juvenile arthritis (PJIA) and systemic juvenil
Therapeutic value Possible equal value
Registration phase Registration application pending

Product

Active substance Tocilizumab
Domain Chronic immune diseases
Reason of inclusion Biosimilar BS
Main indication Rheumatism
Extended indication Rheumatoid arthritis (RA), giant lymph node hyperplasia (Castlesman’s disease), polyarticular idioathic juvenile arthritis (PJIA) and systemic juvenile idiopathic arthritis (SJIA).
Current proprietary name RoActemra (Roche)
Mechanism of action Interleukin inhibitor
Route of administration Unknown
Therapeutical formulation Unknown
Budgetting framework Intermural (MSZ)

Registration

Registration route Centralised (EMA)
Type of trajectory Unknown
Particularity Unknown
ATMP Unknown
Submission date August 2022
Expected Registration August 2023
Orphan drug No
Registration phase Registration application pending
Additional remarks SPC RoActemra verloopt op 6 juni 2020. Er zijn 2 indieningen voor Tocilizumab biosimilars geweest bij de EMA 1 in augustus en 1 in september.

Therapeutic value

Therapeutic value Possible equal value

This assessment does not indicate any potential inclusion in the package.

Expected patient volume per year

Patient volume

Market share is generally not included unless otherwise stated.

Expected cost per patient per year

Potential total cost per year

Off label use

Off label use Unknown

Indication extension

Indication extensions Unknown

Other information