drugset / Trial / NCT05673603

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

NCT05673603

Phase 1 Completed 28 enrolled Insmed Incorporated
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The primary purpose of the study is to determine the pharmacokinetics (PK) following a single oral dose administration of brensocatib, safety, and tolerability of brensocatib when administered to participants with impaired renal function and in healthy participants.

Timeline

Start
2021-07-20
Primary completion
2023-02-14
Completion
2023-02-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Brensocatib Small molecule 25 mg Oral