Extended indication Behandeling van matige (persisterend epitheeldefect) of ernstige (cornea ulcus) neurotrofische keratitis bij volwassenen.
Therapeutic value No judgement
Registration phase Registered

Product

Active substance Cenegermin
Domain Neurological disorders
Main indication Eye disorders
Extended indication Behandeling van matige (persisterend epitheeldefect) of ernstige (cornea ulcus) neurotrofische keratitis bij volwassenen.
Proprietary name Oxervate
Manufacturer DompƩ
Mechanism of action Unknown
Route of administration Ocular
Therapeutical formulation Eye drops
Budgetting framework Extramural (GVS)
Additional remarks Werkingsmechanisme: 'Recombinant human nerve growth factor (rhNGF)'.

Registration

Registration route Centralised (EMA)
Type of trajectory Accelerated assessment
Particularity New medicine
ATMP Unknown
Submission date December 2016
Expected Registration July 2017
Orphan drug Yes
Registration phase Registered
Additional remarks Oxervate is per juli 2017 geregistreerd bij de EMA voor Keratitis. Nog geen vergoeding.

Therapeutic value

Therapeutic value No judgement

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.

References EMA
Additional remarks Neurotrophic keratitis komt voor bij 4.2 in 10,000 inwoners van de EU. Dit zijn 7.140 patiƫnten per 17 miljoen Nederlanders.

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