Brinsupri
- Prescription status not stated
- Breathing, airways, allergies and cough
- Active substance
- Brensocatib
- Made by
- Insmed Netherlands B.V.
- Source
- Official label
Quoted from the official source. Not yet reviewed by Mediclarum — the leaflet in your pack is authoritative.
What it is for
- Brinsupri is indicated for the treatment of non-cystic fibrosis bronchiectasis (NCFB) in patients 12 years of age and older with two or more exacerbations in the prior 12 months.
From the official label · 2026-09-30 · European Medicines Agency
How it works
From the US prescribing label for the same active substance (Brinsupri). It describes the substance, not this exact product.
Brensocatib is a competitive, reversible inhibitor of dipeptidyl peptidase 1 (DPP1).
DPP1 activates pro-inflammatory neutrophil serine proteases (NSPs) during neutrophil maturation in the bone marrow.
Brensocatib is primarily metabolized by CYP3A and to a lesser extent by CYP2C8 and CYP2D6.
Effect of Food No clinically relevant differences in brensocatib pharmacokinetics were observed following administration of brensocatib with a high-fat meal (990 calories, 52% fat).
Quoted from the prescribing label, sections “Mechanism of Action” and “Pharmacokinetics”. DailyMed · 2026-03-16
Same active substance, strength and form in other countries
Matched on active substance, strength and kind of form only. This is not a statement that the products are equivalent or interchangeable: other ingredients, release and approved uses can differ — ask a pharmacist before swapping.
Medicine passport: one printable page to show a pharmacist abroad
United StatesNo exact match for this strength and form
Details
| Made by | Insmed Netherlands B.V. |
|---|---|
| Active substance | Brensocatib |
| Used in | Breathing, airways, allergies and cough |
| Classification | R03 · Breathing, airways, allergies and cough |
| Additional monitoring ▼ | Yes — under additional monitoring (black triangle). Report suspected side effects. |
| Authorised on | 2025-11-18 |
| Last updated by the regulator | 2026-09-16 |
| EMA product number | EMEA/H/C/005820 |
Source: European Medicines Agency — medicine data · 2026-09-30 · not reviewed by a clinician
Source: European Medicines Agency (EMA). Product information as published by EMA. Reuse terms: EMA legal notice (reproduction authorised).