Extended indication Gohibic is indicated for the treatment of adult patients with SARS‑CoV2‑induced acute respiratory distress syndrome (ARDS) who are receiving systemic
Therapeutic value No estimate possible yet
Registration phase Registered

Product

Active substance Vilobelimab
Domain Infectious diseases
Reason of inclusion New medicine (specialité)
Main indication COVID-19
Extended indication Gohibic is indicated for the treatment of adult patients with SARS‑CoV2‑induced acute respiratory distress syndrome (ARDS) who are receiving systemic corticosteroids as part of standard of care and who are receiving invasive mechanical ventilation (IMV) (with or without extracorporeal membrane oxygenation (ECMO)).
Proprietary name Gohibic
Manufacturer Inflarx
Portfolio holder Inflarx
Mechanism of action Complement inhibitor
Route of administration Intravenous
Therapeutical formulation Intravenous drip
Budgetting framework Intermural (MSZ)

Registration

Registration route Centralised (EMA)
ATMP No
Submission date August 2023
Expected Registration January 2025
Orphan drug Yes
Registration phase Registered
Medicine sluice Rejected

Therapeutic value

Current treatment options Tocilizumab
Therapeutic value No estimate possible yet

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

Substantiation Het is een anti-C5a monoklonaal antilichaam dat het complementsysteem remt. Dit zou moeten zorgen voor een lagere mortaliteit bij de eindstadia van COVID-19. Hierdoor is dit geneesmiddel in principe variantonafhankelijk. Er is op dit moment echter nog niet genoeg bewijs om een plaatsbepaling te doen (2).
Dosage per administration 800mg
References NCT04333420 (PANAMO) (1); Expertopinie (2).

Expected patient volume per year

Patient volume

Market share is generally not included unless otherwise stated.

References Coronadashboard. Rijksoverheid (1); Expertopinie (2).
Additional remarks In 2023 waren er 857 intensive care opnames van COVID patiënten (1). Er wordt verwacht dat er mogelijk 100 patiënten behandeld zullen worden met vilobelimab (2).

Expected cost per patient per year

Cost 250,000.00

This amount gives an indication of the total cost. It is the result of the average expected patient volume times the average cost per patient. both per year.

References Drugs.com; IHSI
Additional remarks De prijs voor Vilobelimab intraveneuze oplossing (10mg/mL) is $6.350 voor 80ml. Kosten op basis van IHSI-inschatting, afgeleid van de mediane kosten van dezelfde ATC-klasse (L04AJ) geneesmiddelen.

Potential total cost per year

Off label use

Indication extension

Other information