Extended indication Naxitamab in combination with granulocyte-macrophage colony-stimulating factor for second line treatment of high-risk Neuroblastoma in infants and tod
Therapeutic value No estimate possible yet
Registration phase Clinical trials

Product

Active substance Naxitamab
Domain Oncology
Reason of inclusion New medicine (specialité)
Main indication Brain cancer
Extended indication Naxitamab in combination with granulocyte-macrophage colony-stimulating factor for second line treatment of high-risk Neuroblastoma in infants and toddlers, children, adolescents.
Proprietary name Danyelza
Manufacturer Y-mAbs Therapeutics
Portfolio holder Y-mAbs Therapeutics
Mechanism of action MEK kinase inhibitor
Route of administration Intravenous
Therapeutical formulation Infusion fluid
Budgetting framework Intermural (MSZ)
Additional remarks Werkingmechanisme: gehumaniseerde monoklonale antilichaam gericht tegen het GD2-antigeen.

Registration

Registration route Centralised (EMA)
Type of trajectory Normal trajectory
ATMP No
Submission date July 2026
Expected Registration August 2027
Orphan drug No
Registration phase Clinical trials

Therapeutic value

Therapeutic value No estimate possible yet

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

References NCT03363373 (Study 201)

Expected patient volume per year

Patient volume 7 - 10

Market share is generally not included unless otherwise stated.

References Neuroblastoma. Prinses Maxima Centrum. 2025.
Additional remarks De verwachting is dat jaarlijks ongeveer 25 kinderen in Nederland gediagnosticeerd worden met neuroblastoom. Van deze gevallen wordt geschat dat ongeveer 30 tot 40% als hoog-risico wordt geclassificeerd, wat neerkomt op ongeveer zeven tot tien nieuwe gevallen per jaar.

Expected cost per patient per year

Potential total cost per year

Off label use

Indication extension

Other information