Extended indication In patients with relapsed or metastatic cervical cancer (r/m CC) who have progressed on or after platinum-based chemotherapy
Therapeutic value No estimate possible yet
Registration phase Clinical trials

Product

Active substance Cadonilimab
Domain Oncology
Reason of inclusion New medicine (specialité)
Main indication Cervical cancer
Extended indication In patients with relapsed or metastatic cervical cancer (r/m CC) who have progressed on or after platinum-based chemotherapy
Manufacturer Akeso
Mechanism of action Other, see general comments
Route of administration Intravenous
Therapeutical formulation Intravenous drip
Budgetting framework Intermural (MSZ)
Additional remarks Werkingsmechanisme: PD-1/CTLA-4 bi-specific antibody.

Registration

Registration route Centralised (EMA)
Type of trajectory Unknown
Particularity Unknown
ATMP No
Submission date 2023
Expected Registration 2024
Orphan drug No
Registration phase Clinical trials
Additional remarks In de Verenigde Staten bij de FDA aangemerkt als versnelde beoordeling. In China midden 2022 al goedgekeurd.

Therapeutic value

Current treatment options Bevacizumab
Therapeutic value No estimate possible yet

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

Substantiation Er loopt een RCT fase 3 studie. Het zal nog enige tijd duren voordat de resultaten bekend zijn.
Frequency of administration 1 times every 3 weeks
References NCT05063916, NCT04982237, NCT05235516

Expected patient volume per year

Patient volume < 806

Market share is generally not included unless otherwise stated.

References IKNL (1)
Additional remarks In 2020 waren er 806 patiënten met een cervixcarcinoom.

Expected cost per patient per year

Potential total cost per year

Off label use

Off label use Unknown

Indication extension

Indication extensions Yes
Indication extensions Phase III: Gastric cancer; Liver cancer; Oesophageal cancer
References AdisInsight

Other information