Extended indication Treatment of moderate to severe chronic pain in patients with opioid dependence.
Therapeutic value No estimate possible yet
Registration phase Registration application pending

Product

Active substance Buprenorphine
Domain Neurological disorders
Reason of inclusion Indication extension IND
Main indication Pain
Extended indication Treatment of moderate to severe chronic pain in patients with opioid dependence.
Proprietary name Buvidal
Manufacturer Camurus
Mechanism of action Receptor agonist
Route of administration Subcutaneous
Therapeutical formulation Injection
Budgetting framework Extramural (GVS)

Registration

Registration route Unknown
Type of trajectory Unknown
Particularity Unknown
ATMP Unknown
Submission date November 2021
Expected Registration September 2022
Orphan drug No
Registration phase Registration application pending

Therapeutic value

Therapeutic value No estimate possible yet

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

Expected patient volume per year

Patient volume

Market share is generally not included unless otherwise stated.

Expected cost per patient per year

References https://www.zorginstituutnederland.nl/publicaties/adviezen/2021/07/21/gvs-advies-subcutaan-buprenorfine-buvidal
Additional remarks Er zijn 7 verschillende doseringen beschikbaar: 4 doseringen zijn geschikt voor de wekelijkse toediening en 3 doseringen zijn geschikt voor de maandelijkse toediening. De apotheekinkoopprijs (AIP) is voor alle wekelijkse doseringen gelijk, dit komt neer op €87. Voor alle maandelijkse doseringen komt de AIP uit op €375,88.

Potential total cost per year

Off label use

Off label use Unknown

Indication extension

Indication extensions Unknown

Other information