drugset / Trial / NCT03534622

Evaluate Safety and Pharmacokinetic To Assess Bronchopulmonary Disposition of Intravenous Delafloxacin in Healthy Adults

NCT03534622 ↗

Phase 1 Completed 30 enrolled Melinta Therapeutics, Inc.
NaSingle-groupOpen-labelBasic science

Summary

The purpose of this study is to evaluate the steady-state intrapulmonary disposition of delafloxacin in healthy adult participants.

Timeline

Start
2018-04-30
Primary completion
2018-07-19
Completion
2018-07-27

Outcome

Met primary endpoint

paper Noninferiority of delafloxacin compared with moxifloxacin was demonstrated. PMID 31988972 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Delafloxacin Small molecule 300 mg Intravenous

Indications