Extended indication For information on the full indications for Opdivo solution for injection please refer to the EMA website: https://www.ema.europa.eu/en/medicines/hum
Therapeutic value No estimate possible yet
Registration phase Registered

Product

Active substance Nivolumab/hyaluronidase Ph20
Domain Oncology
Reason of inclusion Indication extension IND
Main indication Kidney cancer
Extended indication For information on the full indications for Opdivo solution for injection please refer to the EMA website: https://www.ema.europa.eu/en/medicines/human/variation/opdivo-4.
Manufacturer BMS
Portfolio holder BMS
Mechanism of action PD-1 / PD-L1 inhibitor
Route of administration Subcutaneous
Therapeutical formulation Intravenous drip
Budgetting framework Intermural (MSZ)
Additional remarks Nieuwe subcutane toedieningsvorm van nivolumab met recombinant humaan hyaluronidase (rHuPH20).

Registration

Registration route Centralised (EMA)
Type of trajectory Normal trajectory
Particularity New therapeutical formulation
ATMP No
Submission date June 2024
Expected Registration May 2025
Orphan drug No
Registration phase Registered
Reimbursement Reimbursed from the basic package
Medicine sluice Out of the sluice
Additional remarks Is in juni 2024 bij EMA ingediend als Extension Application. Positieve CHMP opinie op 27 maart 2025. https://www.ema.europa.eu/en/medicines/human/variation/opdivo-4.

Therapeutic value

Therapeutic value No estimate possible yet

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

Substantiation De volledige resultaten zijn nog niet bekend.
References NCT04810078 (CheckMate-67T)

Expected patient volume per year

Patient volume

Market share is generally not included unless otherwise stated.

Expected cost per patient per year

Potential total cost per year

Off label use

Indication extension

Other information