drugset / Trial / NCT00851435

Safety and Pharmacokinetics of KBPA-101 in Hospital Acquired Pneumonia Caused by O11 Pseudomonas Aeruginosa

NCT00851435

Phase 1/2 Completed 15 enrolled Kenta Biotech Ltd
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The objectives of this open study are to assess the safety, tolerability, pharmacokinetics and clinical outcome of patients who have HAP caused by Pseudomonas aeruginosa serotype O11 after three separate administrations of KBPA-101 every third day in addition of standard of care antibiotic treatment.

Timeline

Start
2008-02
Primary completion
2009-07
Completion
2009-07

Drugs

EvaluationDrugModalityDoseRoute
Subject AR101 Protein / enzyme biologic 1.2 mg/kg Intravenous

Indications