Extended indication Pembrolizumab in combination with gemcitabine and cisplatin followed by surgery and postoperative pembrolizumab for neoadjuvant treatment of non-metas
Therapeutic value No estimate possible yet
Total cost 144,000,000.00
Registration phase Clinical trials

Product

Active substance Pembrolizumab
Domain Oncology
Reason of inclusion Indication extension IND
Main indication Bladder cancer
Extended indication Pembrolizumab in combination with gemcitabine and cisplatin followed by surgery and postoperative pembrolizumab for neoadjuvant treatment of non-metastatic muscle invasive Bladder cancer in adults and elderly who are eligible for radical cystectomy and pelvic lymph node dissection.
Proprietary name Keytruda
Manufacturer MSD
Mechanism of action PD-1 / PD-L1 inhibitor
Route of administration Intravenous
Therapeutical formulation Intravenous drip
Budgetting framework Intermural (MSZ)

Registration

Registration route Centralised (EMA)
Type of trajectory Normal trajectory
ATMP No
Submission date 2026
Expected Registration May 2027
Orphan drug No
Registration phase Clinical trials
Medicine sluice Out of the sluice
Additional remarks Voor alle indicaties van pembrolizumab geldt een financieel arrangement tot 1 januari 2027.

Therapeutic value

Therapeutic value No estimate possible yet

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

Frequency of administration 1 times every 3 weeks
Dosage per administration 200mg
References NCT03924856 (KEYNOTE-866)

Expected patient volume per year

Patient volume < 1,600

Market share is generally not included unless otherwise stated.

References IKNL; expertopinie
Additional remarks Volgens IKNL worden in Nederland jaarlijks ongeveer 5.400 patiënten primair gediagnosticeerd met niet-spier-invasieve blaaskanker (NMIBC) - dit betreft Ta-, T1- en CIS-laesies. 1.600 patiënten krijgen primair de diagnose spier-invasieve blaaskanker (MIBC).

Expected cost per patient per year

Cost < 90,000.00

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.

Additional remarks Voor pembrolizumab is een financieel arrangement van toepassing tot 1 januari 2027. Aankomende indicatie uitbreidingen vallen onder deze overeenkomst, mits zij voldoen aan stand der wetenschap en praktijk. AIP per juni 2026: €2.624,38 per injectieflacon 25MG/ML FL 4ML (oplossing). Uitgaande van een behandeling van 1 x per 3 weken 200 mg voor 12 maanden zou dat gaan om maximaal €90.000 per patiënt per jaar. Inschatting: in lijn met andere indicaties.

Potential total cost per year

Total cost 144,000,000.00

Off label use

Indication extension

Other information