Extended indication Tadekinig alfa monotherapy for add-on treatment of primary monogenic IL-18 driven Haemophagocytic lymphohistiocytosis in children, adolescents and adu
Therapeutic value No estimate possible yet
Registration phase Clinical trials

Product

Active substance Tadekinig alfa
Domain Chronic immune diseases
Reason of inclusion New medicine (specialité)
Main indication Other chronic immune diseases
Extended indication Tadekinig alfa monotherapy for add-on treatment of primary monogenic IL-18 driven Haemophagocytic lymphohistiocytosis in children, adolescents and adults with NLRC4 mutation or XIAP deficiency.
Manufacturer Ab2
Mechanism of action Immunosuppression
Route of administration Subcutaneous
Therapeutical formulation Suspension for cutaneous use
Budgetting framework Extramural (GVS)

Registration

Registration route Centralised (EMA)
Type of trajectory Normal trajectory
ATMP No
Submission date September 2026
Expected Registration October 2027
Orphan drug Yes
Registration phase Clinical trials
Additional remarks Tijdslijn op basis van IHSI-inschatting.

Therapeutic value

Therapeutic value No estimate possible yet

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

References NCT03113760; NCT03512314

Expected patient volume per year

Patient volume

Market share is generally not included unless otherwise stated.

Expected cost per patient per year

Additional remarks Er is nog niets bekend over de mogelijke prijs.

Potential total cost per year

Off label use

Indication extension

Other information