Extended indication Darunavir/cobicistat/emtricitabine/tenofovir alafenamide combination therapy for treatment of HIV-1 infection in children over 6 years of age with bod
Therapeutic value No estimate possible yet
Registration phase Registration application pending

Product

Active substance Darunavir / cobicistat / emtricitabine / tenofovir alafenamide
Domain Infectious diseases
Reason of inclusion Indication extension IND
Main indication HIV
Extended indication Darunavir/cobicistat/emtricitabine/tenofovir alafenamide combination therapy for treatment of HIV-1 infection in children over 6 years of age with body weight at least 25kg.
Proprietary name Symtuza
Manufacturer Janssen
Route of administration Oral
Therapeutical formulation Tablet
Budgetting framework Extramural (GVS)

Registration

Registration route Centralised (EMA)
Type of trajectory Normal trajectory
ATMP No
Submission date February 2025
Expected Registration July 2026
Orphan drug No
Registration phase Registration application pending

Therapeutic value

Current treatment options Een combinatie van twee NRTI’s + een INSTI
Therapeutic value No estimate possible yet

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

Substantiation Voor deze groep is darunavir / cobicistat / emtricitabine / tenofovir alafenamide niet het eerste keus medicament. Dit is mogelijk wel een goede single tablet regimen indien er HIV-resistentie is (met name tegen INSTI) of bij bijwerkingen tegen andere middelen.
References NCT02016924 (GS-US-216-0128); Expertopinie

Expected patient volume per year

Patient volume 5 - 10

Market share is generally not included unless otherwise stated.

References Expertopinie
Additional remarks In Nederland zijn er tussen de vijf en tien patiënten tussen de zes en twaalf jaar oud met HIV/AIDS.

Expected cost per patient per year

Potential total cost per year

Off label use

Indication extension

Other information