Extended indication Pembrolizumab in combination with paclitaxel with or without bevacizumab for second line or later treatment of platinum-resistant Ovarian cancer recur
Therapeutic value No estimate possible yet
Registration phase Clinical trials

Product

Active substance Pembrolizumab
Domain Oncology
Reason of inclusion Indication extension IND
Main indication Ovarian cancer
Extended indication Pembrolizumab in combination with paclitaxel with or without bevacizumab for second line or later treatment of platinum-resistant Ovarian cancer recurrent in adults and elderly.
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
Particularity Unknown
ATMP No
Submission date September 2025
Expected Registration March 2026
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.

Dosage per administration 400mg
References NCT05116189 (KEYNOTE-B96/ENGOT-ov65)

Expected patient volume per year

Patient volume < 180

Market share is generally not included unless otherwise stated.

References (1) IKNL; (2) expertopinie
Additional remarks In Nederland werden in 2022 ongeveer 1.400 vrouwen gediagnosticeerd met eierstokkanker (1) (ovariumcarcinoom). Platinumresistent ovariumcarcinoom betreft tot 20% van de patiƫnten (280 patiƫnten) (2).

Expected cost per patient per year

Additional remarks Voor alle indicaties van pembrolizumab geldt een financieel arrangement.

Potential total cost per year

Off label use

Off label use Unknown

Indication extension

Indication extensions Unknown

Other information