drugset / Trial / NCT03091439

Safety and Efficacy of Dalbavancin Versus Active Comparator in Adult Patients With Osteomyelitis

NCT03091439

Phase 2 Terminated 1 enrolled Allergan
RandomizedParallel-groupOpen-labelTreatment

Summary

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

Timeline

Start
2017-05-15
Primary completion
2017-08-31
Completion
2017-08-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Dalbavancin Other / unclassified 1500 mg Intravenous

Indications