Extended indication Dordaviprone monotherapy for treatment of newly diagnosed H3 K27M-mutant diffuse glioma in children, adolescents, adults and elderly following complet
Therapeutic value No estimate possible yet
Registration phase Clinical trials

Product

Active substance Dordaviprone
Domain Oncology
Reason of inclusion New medicine (specialité)
Main indication Brain cancer
Extended indication Dordaviprone monotherapy for treatment of newly diagnosed H3 K27M-mutant diffuse glioma in children, adolescents, adults and elderly following completion of radiotherapy.
Manufacturer Chimerix
Route of administration Oral
Therapeutical formulation Capsule
Budgetting framework Intermural (MSZ)

Registration

Registration route Centralised (EMA)
Type of trajectory Normal trajectory
ATMP No
Submission date November 2026
Expected Registration December 2027
Orphan drug Yes
Registration phase Clinical trials
Additional remarks Indieningsdatum en verwachte registratie aan de hand van IHSI-inschatting.

Therapeutic value

Current treatment options Bestraling
Therapeutic value No estimate possible yet

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

Frequency of administration 1 times every 2 weeks
Dosage per administration 625mg
References NCT05580562 (ACTION)
Additional remarks Patiënten met een gewicht van meer dan 52,5kg: 625mg eenmaal per een of twee weken. Patiënten met een gewicht van minder dan 52,5 kg: een dosering (en bijbehorende aantal capsules) aangepast aan lichaamsgewicht en afgerond tot incrementen van 125mg.

Expected patient volume per year

Patient volume 8 - 10

Market share is generally not included unless otherwise stated.

References El-Khouly. PhD-Thesis Vrije Universiteit Amsterdam. 2022 (1)
Additional remarks Jaarlijks krijgen acht tot tien kinderen in Nederland de diagnose diffuus intrinsiek ponsglioom (DIPG) (1).

Expected cost per patient per year

Potential total cost per year

Off label use

Indication extension

Other information