Extended indication Treatment of adult patients with Philadelphia chromosome-positive chronic myeloid leukaemia in chronic phase (Ph+ CML-CP) harbouring the T315I mutation.
Therapeutic value No estimate possible yet
Registration phase Registration application pending

Product

Active substance Asciminib
Domain Hematology
Reason of inclusion Indication extension IND
Main indication CML
Extended indication Treatment of adult patients with Philadelphia chromosome-positive chronic myeloid leukaemia in chronic phase (Ph+ CML-CP) harbouring the T315I mutation.
Proprietary name Scemblix
Manufacturer Novartis
Portfolio holder Novartis
Mechanism of action Tyrosine kinase inhibitor
Route of administration Oral
Therapeutical formulation Tablet
Budgetting framework Intermural (MSZ)

Registration

Registration route Centralised (EMA)
Type of trajectory Normal trajectory
Particularity Unknown
ATMP No
Submission date March 2025
Expected Registration January 2026
Orphan drug Yes
Registration phase Registration application pending

Therapeutic value

Current treatment options Tweede generatie TKI.
Therapeutic value No estimate possible yet

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

References NCT02081378 (CABL001X2101)

Expected patient volume per year

Patient volume

Market share is generally not included unless otherwise stated.

Expected cost per patient per year

References medicijnkosten.nl
Additional remarks SCEMBLIX, 80 mg € 145,33 gemiddelde prijs per dag.

Potential total cost per year

Off label use

Off label use Unknown

Indication extension

Indication extensions Unknown

Other information