Single Administration of KBSA301 in Patients with Severe Pneumonia.
Research type
Research Study
Full title
A Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose Group Study to assess the Safety, Tolerability, Pharmacokinetics, Efficacy and Pharmacodynamics of a Single Intravenous Administration of KBSA301 in Severe Pneumonia caused by Staphylococcus aureus
IRAS ID
97213
Contact name
Barbara Philips
Contact email
Sponsor organisation
Kenta Biotech Ltd
Eudract number
2011-005268-43
ISRCTN Number
n.a
Clinicaltrials.gov Identifier
n.a
Research summary
The main purpose of this study is to assess the safety and tolerability of single ascending doses of KBSA301 in patients with severe pneumonia caused by S. aureus and treated with standard S. aureus antibiotic therapy.
REC name
East of England - Cambridge East Research Ethics Committee
REC reference
12/EE/0127
Date of REC Opinion
24 May 2012
REC opinion
Further Information Favourable Opinion