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Comparison · NCT03840148-e6e4b182

Cefepime/VNRX-5133 (Taniborbactam) vs Meropenem: Microbiologic Success at Test of Cure (TOC) in the microITT Population

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Cefepime/VNRX-5133 (Taniborbactam) vs Meropenem: Microbiologic Success at Test of Cure (TOC) in the microITT Population. Trial comparisons, record NCT03840148-e6e4b182. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03840148-e6e4b182

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.7820.7310.825wilson
Risk in group 20.6640.5840.737wilson
Risk difference, group 1 minus group 20.1170.0290.209newcombe hybrid score
Risk ratio, group 1 over group 21.181.031.34log
Odds ratio, group 1 over group 21.811.162.82log
Number needed to treat, for one more participant with the outcome on Cefepime/VNRX-5133 (Taniborbactam) than on Meropenem8.534.7834.5from the risk difference interval

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Cefepime/VNRX-5133 (Taniborbactam)Cefepime/VNRX-5133 administered q8h intravenously (IV) over a 2-hour period.229293OG000
Group 2MeropenemMeropenem will be administered q8h IV over 30 minutes.95143OG001

Outcome

Type
SECONDARY
Title
Microbiologic Success at Test of Cure (TOC) in the microITT Population
Description
Microbiologic success is eradication defined as demonstration that any gram-negative bacterial pathogen found at study entry (≥10\^5 CFU/mL) is eradicated to \<10\^3 CFU/mL.
Time frame
Assessed at Test of Cure visit (occurred once per participant between Study Days 19 to 23)
Population
The microITT analysis population consists of all patients in the ITT analysis population who had a positive study entry urine culture defined as ≥10\^5 CFU/mL of a gram-negative pathogen(s) against which both cefepime/VNRX-5133 and meropenem have antibacterial activity AND those patients who had no more than 2 microorganisms identified in the study entry culture regardless of colony count.

Source ClinicalTrials.gov

Trial

Title
Safety and Efficacy Study of Cefepime/VNRX-5133 in Patients With Complicated Urinary Tract Infections
NCT number
NCT03840148
Phases
PHASE3
Conditions
Urinary Tract Infections, Acute Pyelonephritis
Interventions
Cefepime/VNRX-5133 (taniborbactam), Meropenem
Lead sponsor
Venatorx Pharmaceuticals, Inc.
Results first posted
2024-05-29

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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