Extended indication Selumetinib monotherapy for first line treatment of symptomatic inoperable plexiform neurofibroma in adults and elderly with neurofibromatosis type 1.
Therapeutic value No estimate possible yet
Registration phase Clinical trials

Product

Active substance Selumetinib
Domain Oncology
Reason of inclusion Indication extension IND
Main indication Oncology other
Extended indication Selumetinib monotherapy for first line treatment of symptomatic inoperable plexiform neurofibroma in adults and elderly with neurofibromatosis type 1.
Proprietary name Koselugo
Manufacturer Alexion
Portfolio holder Alexion
Mechanism of action MEK kinase inhibitor
Route of administration Oral
Therapeutical formulation Capsule
Budgetting framework Intermural (MSZ)
Centre of expertise Erasmus MC

Registration

Registration route Centralised (EMA)
Type of trajectory Normal trajectory
Particularity Unknown
ATMP No
Submission date 2025
Expected Registration 2026
Orphan drug Yes
Registration phase Clinical trials

Therapeutic value

Therapeutic value No estimate possible yet

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

Frequency of administration 2 times a day
Dosage per administration 25mg/m2 BSA
References NCT04924608 (KOMET)

Expected patient volume per year

Patient volume

Market share is generally not included unless otherwise stated.

Expected cost per patient per year

Cost < 267,402.00

This amount gives an indication of the total cost. It is the result of the average expected patient volume times the average cost per patient. both per year.

References Advies - vergoed selumetinib (Koselugo®) voor de behandeling van goedaardige tumoren bij kinderen met neurofibromatose type 1 (NF1). Zorginstituut Nederland. 2024 (1).
Additional remarks Een behandeling voor een patiënt met een gemiddeld lichaamsoppervlak van 1,70m2 kost €267.402 per patiënt per jaar (1).

Potential total cost per year

Off label use

Off label use Unknown

Indication extension

Indication extensions No

Other information