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28 April 2024 - P2522
Outcomes at test of cure by baseline pathogen and cefepime-taniborbactam or meropenem MIC in the Phase 3 CERTAIN-1 study of patients with complicated urinary tract infection (cUTI)
04 October 2022 - EA01
Time to change the complicated urinary tract infection primary endpoint? The problem and a potential solution
04 October 2022 - EA03
Cefepime-taniborbactam and comparator activity in vitro against carbapenem-resistant Enterobacterales (CRE), carbapenem-resistant P. aeruginosa (CRPA) and multidrug-resistant (MDR) Enterobacterales and P. aeruginosa from 2018-2020 global surveillance
09 July 2021 - 3285
Assessment of activity of a novel orally bioavailable β-lactam/β-lactamase inhibitor combination, ceftibuten/VNRX-7145 (VNRX-5236 etzadroxil) against Enterobacterales carrying blaOXA-48
09 July 2021 - 2128
Cefepime/taniborbactam (formerly cefepime/VNRX-5133) demonstrates potent activity versus Enterobacterales with blaOXA-48
09 July 2021 - 2144
Examining the antimicrobial activity of cefepime/taniborbactam (formerly cefepime/VNRX-5133) against Burkholderia species isolated from cystic fibrosis patients in the United States
14 April 2019 - P1183
Oral ceftibuten/VNRX-7145 shows equivalent activity in vitro to IV therapeutics against MDR Enterobacteriaceae
14 April 2019 - P1181
Selection of ceftibuten as the partner antibiotic for the oral beta-lactamase inhibitor VNRX-7145
26 April 2015 - P0713
Oritavancin disk diffusion assay can distinguish vancomycin-intermediate Staphylococcus aureus from vancomycin-susceptible S. aureus
26 April 2015 - P0709
Oritavancin and comparator activities against S. aureus and Streptococcus spp. isolated from skin and skin structure infections in Europe and North America 2011-2014
12 May 2014 - O152
A single dose of oritavancin (ORI) compared to 7-10 days of vancomycin (VAN): clinical response across different lesion types in the SOLO non-inferiority studies
10 May 2014 - eP418
Concordance between early (48-72 hours) and late (7-14 days post therapy) clinical response: an analysis from the solo non-inferiority clinical studies
10 May 2014 - eP174
Oritavancin does not antagonise the activity of common antibacterial agents for Gram-positive and Gram-negative infections
10 May 2014 - eP173
Longitudinal study of the activity of oritavancin (ORI) against Staphylococcus aureus (SA) from Europe (EU) between 2011 and 2013
10 May 2014 - eP416
Clinical outcomes by pathogen in phase 3 studies of single dose oritavancin versus 7 to 10 days of vancomycin to treat CSSTI
10 May 2014 - eP417
The PVL gene does not impact clinical response to treatment with single dose oritavancin or 7 to 10 days of vancomycin in patients with CSSTI
28 April 2013 - P1594
In vitro activities of oritavancin and comparators against methicillin-resistant Staphylococcus aureus (MRSA) strains harbouring the novel mecC gene
28 April 2013 - P1644
Activity of oritavancin against European bacterial pathogens associated with skin/wound and soft tissue infections and bacteraemia
28 April 2013 - P1645
Activity of oritavancin against European Gram-positive bacterial pathogens with problematic resistant phenotypes
28 April 2013 - P1605
Development of disc diffusion method for oritavancin: comparison of disc diffusion with broth microdilution reference method for Staphylococcus aureus
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