Extended indication diffuse large B-cell lymphoma (based on study ESCALADE- ACE-LY-312)); Acalabrutinib in Combination With Rituximab, Cyclophosphamide, Doxorubicin, Vinc
Therapeutic value No estimate possible yet
Registration phase Clinical trials

Product

Active substance Acalabrutinib
Domain Oncology
Reason of inclusion Indication extension IND
Main indication Oncology other
Extended indication diffuse large B-cell lymphoma (based on study ESCALADE- ACE-LY-312)); Acalabrutinib in Combination With Rituximab, Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone (R-CHOP) in Subjects ≤75 Years With Previously Untreated Non-GCB DLBCL.
Proprietary name calquence
Manufacturer AstraZeneca
Portfolio holder AstraZeneca
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
ATMP No
Submission date 2026
Expected Registration 2027
Orphan drug No
Registration phase Clinical trials
Medicine sluice Broadly excluded

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 100 mg
References https://www.astrazenecaclinicaltrials.com/study/D8227C00001/

Expected patient volume per year

Patient volume 800

Market share is generally not included unless otherwise stated.

References 1: NKR2022;
Additional remarks De incidentie van DLBCL (en varianten) in Nederland in 2022 was 1.606 patiënten (1). Ongeveer 50% van de patiënten heeft het non-GCB subtype. Dit betekent dat er per jaar ongeveer 800 patiënten met DLBCL in aanmerking zouden kunnen komen voor behandeling met ibrutinib.

Expected cost per patient per year

Additional remarks kosten per tablet van 100mg is €75,39, dus kosten per dag zijn €150,80.

Potential total cost per year

Off label use

Indication extension

Other information