Extended indication Padeliporfin monotherapy for first line treatment of low grade non-invasive Renal pelvis and ureter transitional cell cancer localized in adults and e
Therapeutic value No estimate possible yet
Registration phase Clinical trials

Product

Active substance Padeliporfin
Domain Oncology
Reason of inclusion Indication extension IND
Main indication Bladder cancer
Extended indication Padeliporfin monotherapy for first line treatment of low grade non-invasive Renal pelvis and ureter transitional cell cancer localized in adults and elderly.
Proprietary name Tookad
Manufacturer Steba
Route of administration Intravenous
Therapeutical formulation Injection
Budgetting framework Intermural (MSZ)

Registration

Registration route Centralised (EMA)
ATMP No
Submission date June 2026
Expected Registration December 2026
Orphan drug No
Registration phase Clinical trials
Additional remarks Tijdslijn op basis van IHSI-inschatting.

Therapeutic value

Therapeutic value No estimate possible yet

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

Substantiation Er is geen RCT fase 3 studie. Intensieve follow up noodzakelijk. Behoorlijke toxiciteit.
Dosage per administration 3,66mg/kg
References NCT04620239; ENLIGHTED phase 3 study: Efficacy and safety of padeliporfin vascular targeted photodynamic therapy (VTP) for treatment of low-grade upper tract urothelial cancer (LG UTUC). (https://ascopubs.org/doi/10.1200/JCO.2024.42.16_suppl.TPS4622).

Expected patient volume per year

Patient volume < 120

Market share is generally not included unless otherwise stated.

References IKNL2021(1); expertopinie (2)
Additional remarks In 2021 waren er 1.453 gevallen van stadium een nier-cel carcinoma en 24 gevallen van stadium een carcinoom van de urethra. 350 per jaar hebben uppertract, waarvan een derde van deze groep low risk is (120 patiƫnten per jaar) (2).

Expected cost per patient per year

Potential total cost per year

Off label use

Indication extension

Other information