Brensocatib

Drug

Drug Profile

Brensocatib is a once-daily oral DPP1 inhibitor marketed as BRINSUPRI for non-cystic fibrosis bronchiectasis. It is designed to reduce neutrophil-driven airway inflammation and has become the first approved treatment for this disease area in both the U.S. and EU according to the cited source. It is approved for patients aged 12 years and older.

Drug Class
First-in-class DPP1 inhibitor
Approval Status
FDA approved in the U.S. and European Commission approved in the EU (Nov 18, 2025 announcement)
Mechanism of Action
Reversible inhibition of DPP1 to inhibit activation of neutrophil serine proteases, reducing chronic airway inflammation
Brand Names
  • BRINSUPRI
Indications
  • \Non-cystic fibrosis bronchiectasis in patients 12 years and older\

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Related Clinical Trials

NCT ID Title Status Phase
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A Study of the Palatability and Acceptability of Different Brensocatib Oral Liquid Formulations in Healthy Participants

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A Study to Investigate Effect of Clarithromycin, a Strong CYP3A4 Inhibitor, on Brensocatib Pharmacokinetics in Healthy Participants

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NCT05826574

A Study to Assess Pharmacokinetics (PK) of Brensocatib Alone and With Multiple Doses of Rifampin or Esomeprozole in Healthy Participants

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NCT05673603

A Study of Brensocatib Following a Single Oral Administration in Participants With or Without Renal Impairment

COMPLETED PHASE1
NCT05517525

A Study to Evaluate the Pharmacokinetics (PK) and Safety of a Single Dose of Brensocatib in Participants With Normal Hepatic Function and Participants With Hepatic Impairment

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NCT05355935

A Study to Investigate the Effects of Brensocatib on QT Interval in Healthy Participants

COMPLETED PHASE1
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An Expanded Access Study to Assess Brensocatib for Participants With Non-Cystic Fibrosis Bronchiectasis

APPROVED_FOR_MARKETING
NCT05090904

A Study to Assess the Safety, Tolerability, and Pharmacokinetics of Brensocatib Tablets in Adults With Cystic Fibrosis

COMPLETED PHASE2