drugset / Trial / NCT02685033

Study on the Safety and Efficacy of Dalbavancin Versus Active Comparator in Adult Participants With Osteomyelitis

NCT02685033

RandomizedParallel-groupOpen-labelTreatment

Summary

This clinical study will be a single-center, randomized, open-label, active-controlled, parallel-group study comparing dalbavancin to standard of care (SOC) therapy in osteomyelitis.

Timeline

Start
2016-03-15
Primary completion
2017-12-12
Completion
2017-12-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Dalbavancin Other / unclassified 1000 mg Intravenous
Subject Dalbavancin Other / unclassified 1500 mg Intravenous

Indications