Extended indication 4L Relapsed/refractory Multiple Myeloma
Therapeutic value No judgement
Registration phase Clinical trials

Product

Active substance GSK2857916
Domain Oncology and Hematology
Reason of inclusion New medicine (specialité)
Main indication Multiple Myeloma
Extended indication 4L Relapsed/refractory Multiple Myeloma
Manufacturer GSK
Mechanism of action Antibody-drug conjugate
Route of administration Intravenous
Therapeutical formulation Intravenous drip
Budgetting framework Intermural (MSZ)
Additional remarks humanized IgG1, an Antibody Drug Conjugated to Microtubule-Disrupting Agent Directed Against B-Cell Maturation Antigen (BCMA).

Registration

Registration route Centralised (EMA)
Type of trajectory Accelerated assessment
Particularity New medicine with Priority Medicines (PRIME)
ATMP Unknown
Submission date August 2019
Expected Registration August 2020
Orphan drug Unknown
Registration phase Clinical trials

Therapeutic value

Therapeutic value No judgement

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

Frequency of administration 1 times every 3 weeks
References NCT03525678

Expected patient volume per year

Patient volume

Market share is generally not included unless otherwise stated.

References NKR
Additional remarks NKR (2015): 1.242 patienten met multipel myeloma(max). Gezien relapsed / refractory en overige behandelingen zal het realistische volume echter een stuk lager liggen.

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 3L, 2L, 1L
References https://www.gsk.com/media/5028/q2-2018-slides-hal-barron.pdf

Other information