drugset / Trial / NCT05955586

A Study to Assess the Intrapulmonary Pharmacokinetics (PK) of SPR719 by Comparing the Plasma, Epithelial Lining Fluid, and Alveolar Macrophage Concentrations Following the Oral Administration of Multiple Doses of SPR720 in Healthy Volunteers.

NCT05955586

Phase 1 Completed 33 enrolled Spero Therapeutics
NaSingle-groupOpen-labelTreatment

Summary

The primary purpose of this study is to evaluate the intrapulmonary PK, including epithelial lining fluid (ELF) and alveolar macrophages (AM) concentrations, of SPR719 compared to plasma concentrations of SPR719 (the active moiety in plasma of the prodrug SPR720) after oral administration of SPR720 1000 milligram (mg) capsules every 24 hours for 7 consecutive doses.

Timeline

Start
2023-08-01
Primary completion
2024-02-09
Completion
2024-02-23

Drugs

EvaluationDrugModalityDoseRoute
Subject SPR720 Small molecule 1000 mg Oral

Indications

No indication recorded.