Extended indication Guillain-Barré Syndrome
Therapeutic value No estimate possible yet
Registration phase Clinical trials

Product

Active substance Tanruprubart
Domain Neurological disorders
Reason of inclusion New medicine (specialité)
Main indication Muscular diseases other
Extended indication Guillain-Barré Syndrome
Manufacturer Annexon
Route of administration Intravenous
Therapeutical formulation Intravenous drip
Budgetting framework Intermural (MSZ)
Additional remarks Complement C1 inhibitor

Registration

Registration route Centralised (EMA)
ATMP No
Submission date February 2026
Expected Registration March 2027
Orphan drug No
Registration phase Clinical trials
Additional remarks Primary completion datum fase 3 studie in april 2024.

Therapeutic value

Current treatment options IVIg is de therapie van eerste keuze bij de behandeling van Guillain-Barré Syndrome (GBS).
Therapeutic value No estimate possible yet

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

Substantiation Nog geen resultaten gepubliceerd. Aangezien het een eenmalige behandeling is en de prijs daarmee wellicht acceptabel kan blijven zal het potentieel IVIg kunnen gaan vervangen indien effectiviteit bevestigd wordt.
Dosage per administration 30mg/kg of 75mg/kg
References NCT04701164 (ANX005-GBS-02)

Expected patient volume per year

Patient volume < 200

Market share is generally not included unless otherwise stated.

References Richtlijnendatabase.nl
Additional remarks GBS is de meest frequente oorzaak van acute spierzwakte in de westerse wereld. De incidentie in Nederland bedraagt 1.3 op de 100.000 per jaar. Dat betekent dat er in Nederland per jaar ongeveer 200 mensen GBS krijgen.

Expected cost per patient per year

Potential total cost per year

Off label use

Indication extension

Other information