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Dalbavancin vs Comparator in Pediatric Subjects With Acute Hematogenous Osteomyelitis — AHOM  

Osteomyelitis Clinical Trial

Official title:
A Phase 3, Multicenter, Double-Blind, Randomized, Comparator Controlled Trial of the Safety and Efficacy of Dalbavancin Versus Active Comparator in Pediatric Subjects With Acute Hematogenous Osteomyelitis of the Long Bones Known or Suspected to be Due to Gram-Positive Organisms

Clinical Trial Summary

Dalbavancin for Pediatric Osteomyelitis

Clinical Trial Description

A Phase 3, Multicenter, Double-Blind, Randomized, Comparator Controlled Trial of the Safety and Efficacy of Dalbavancin versus Active Comparator in Pediatric Subjects with Acute Hematogenous Osteomyelitis of the Long Bones Known or Suspected to be due to Gram-Positive Organisms. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02344511
Study type Interventional
Source Durata Therapeutics Inc., an affiliate of Allergan plc
Contact
Status Withdrawn
Phase Phase 3
Start date March 2016
Completion date April 2019
View Details
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