drugset / Trial / NCT01589185
Safety, Pharmacokinetics and Efficacy of KBSA301 in Severe Pneumonia (S. Aureus)
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |