drugset / Trial / NCT05673603
A Study of Brensocatib Following a Single Oral Administration in Participants With or Without Renal Impairment
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Brensocatib | Small molecule | 25 mg | Oral |