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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

Completed Phase 1 Last updated 21 August 2023
What this trial tests

Phase 1 trial testing Brensocatib in Healthy Volunteers in 32 participants. Completed in 16 July 2023.

Timeline
10 May 2023
Primary endpoint
16 July 2023
16 July 2023

Quick facts

Lead sponsorInsmed Incorporated
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment32
Start date10 May 2023
Primary completion16 July 2023
Estimated completion16 July 2023
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Insmed Incorporated — full company profile →

Who can join

Adults 18 to 55, any sex, with Healthy Volunteers. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary purpose of this study is to assess the effects of rifampin on the PK of brensocatib in Part 1 of the study and to assess the effects of esomeprazole on the PK of brensocatib in Part 2 of the study.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Cathepsin C in health and disease: from structural insights to therapeutic prospects.
    Chitsamankhun C, Siritongtaworn N, Fournier BPJ, Sriwattanapong K, et al · · 2024 · cited 15× · PMID 39164687 · DOI 10.1186/s12967-024-05589-7

Verify or expand the search:

Other trials of Brensocatib

Trials testing the same drug.

Other recruiting trials for Healthy Volunteers

Currently open trials in the same condition.

Other Insmed Incorporated trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05826574.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing