Extended indication Paroxysmal nocturnal haemoglobinuria (PNH) and atypical hemolytic uremic syndrome (aHUS).
Therapeutic value Possible equal value
Registration phase Clinical trials

Product

Active substance Eculizumab
Domain Cardiovascular diseases
Reason of inclusion Biosimilar BS
Main indication Other non-oncological hematological medications
Extended indication Paroxysmal nocturnal haemoglobinuria (PNH) and atypical hemolytic uremic syndrome (aHUS).
Current proprietary name Soliris (Alexion)
Proprietary name ABP 959
Manufacturer Amgen
Mechanism of action Immunosuppression
Route of administration Unknown
Therapeutical formulation Unknown
Budgetting framework Unknown

Registration

Registration route Centralised (EMA)
Type of trajectory Unknown
Particularity Unknown
ATMP Unknown
Orphan drug Yes
Registration phase Clinical trials
Additional remarks Momenteel loopt er een fase 3 studie (EudraCT Number: 2017-001418-27). SPC Soliris verloopt op 30 april 2020. Voor alle indicaties van Soliris registratie geldt een financieel arrangement dat afloopt per eind 2025.

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