drugset / Trial / NCT05369052

Safety and Efficacy Study of Contezolid Acefosamil and Contezolid Compared to Linezolid Administered Intravenously and Orally to Adults With Moderate or Severe Diabetic Foot Infections (DFI)

NCT05369052

Phase 3 Recruiting 865 enrolled MicuRx
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a Phase 3, multicenter, randomized, double-blind, safety and efficacy study of contezolid acefosamil (IV)/contezolid (PO) compared with linezolid (IV and PO) administered for a total of 14 to 28 days in adult subjects with moderate or severe DFI.

Timeline

Start
2022-05-03
Primary completion
2026-06-30
Completion
2026-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Contezolid Small molecule Oral
Comparator Linezolid Other / unclassified Intravenous
Subject contezolid acefosamil Unknown Intravenous

Indications

No indication recorded.