drugset / Trial / NCT01589185

Safety, Pharmacokinetics and Efficacy of KBSA301 in Severe Pneumonia (S. Aureus)

NCT01589185 ↗

Phase 1/2 Completed 48 enrolled Aridis Pharmaceuticals, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The objectives of this study are to assess the safety, tolerability, pharmacokinetics, pharmacodynamics and clinical outcome of patients who have severe pneumonia caused by Staphylococcus aureus (S. aureus) after a single intravenous administration of KBSA301 in addition of standard of care antibiotic treatment.

Timeline

Start
2012-05
Primary completion
2016-05
Completion
2016-09

Drugs

EvaluationDrugModalityDoseRoute
Subject tosatoxumab Monoclonal antibody 1 mg/kg Intravenous
Subject tosatoxumab Monoclonal antibody 3 mg/kg Intravenous
Subject tosatoxumab Monoclonal antibody 10 mg/kg Intravenous
Subject tosatoxumab Monoclonal antibody 20 mg/kg Intravenous