Extended indication Idiopathic Pulmonary Fibrosis (IPF)
Therapeutic value No estimate possible yet
Registration phase Clinical trials

Product

Active substance Zinpentraxin alfa
Domain Lung diseases
Reason of inclusion New medicine (specialité)
Main indication Lung diseases other
Extended indication Idiopathic Pulmonary Fibrosis (IPF)
Manufacturer Roche
Portfolio holder Roche
Mechanism of action Unknown
Route of administration Intravenous
Therapeutical formulation Intravenous drip
Budgetting framework Intermural (MSZ)
Additional remarks A recombinant form of human pentraxin-2 protein able to regulate monocytes and macrophages at areas of tissue damage to prevent and reverse fibrosis.

Registration

Registration route Centralised (EMA)
Type of trajectory Unknown
Particularity Unknown
ATMP No
Submission date 2024
Expected Registration 2025
Orphan drug Yes
Registration phase Clinical trials

Therapeutic value

Therapeutic value No estimate possible yet

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

Frequency of administration 1 times every 4 weeks
Dosage per administration 10 mg/kg
References NCT04594707, NCT04552899

Expected patient volume per year

Patient volume < 2,040

Market share is generally not included unless otherwise stated.

References Jaarverslag Longfibrosepatiëntenvereniging 2017 (1)
Additional remarks Er zijn ongeveer 3.400 longfibrose patiënten in Nederland 60% daarvan heeft IPF. Dit komt neer op 2.040 IPF patiënten.

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 Phase II: Myelofibrosis
References SPS UK

Other information