Extended indication Patients With Previously Treated Metastatic PD-L1 Positive Colorectal Cancer
Therapeutic value No estimate possible yet
Registration phase Clinical trials

Product

Active substance Pembrolizumab / favezelimab
Domain Oncology
Reason of inclusion New medicine (specialité)
Main indication Colon cancer
Extended indication Patients With Previously Treated Metastatic PD-L1 Positive Colorectal Cancer
Manufacturer MSD
Portfolio holder MSD
Mechanism of action Combination therapy
Route of administration Intravenous
Therapeutical formulation Unknown
Budgetting framework Intermural (MSZ)
Additional remarks Co-formulation of PD-1 inhibitor and LAG-3 inhibitor

Registration

Registration route Centralised (EMA)
Type of trajectory Unknown
Particularity New therapeutical formulation
ATMP No
Submission date 2024
Expected Registration 2025
Orphan drug No
Registration phase Clinical trials

Therapeutic value

Current treatment options TAS-102
Therapeutic value No estimate possible yet

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

Duration of treatment Maximal 2 year / years
Frequency of administration 1 times every 3 weeks
Dosage per administration favezelimab/pembrolizumab 800mg/200mg
References NCT05064059
Additional remarks Bispecifiek antilichaam tegen PD-L1 en LAG3 en stimuleert tumorcel afbraak Tcellen via dendritische celactivatie. De Fase 3 studie loopt nog. Fase 1 laten geringe respons zien en te managen toxiciteit.

Expected patient volume per year

Patient volume < 2,085

Market share is generally not included unless otherwise stated.

References NKR2021(1);
Additional remarks Gemetastaseerde coloncarcinoom betreft 2.085 patiënten in stadium 4 (1).

Expected cost per patient per year

Potential total cost per year

Off label use

Off label use Unknown

Indication extension

Indication extensions Unknown

Other information