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Comparison · NCT02208063-deaths

Telavancin vs Standard of Care: deaths from any cause

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. Telavancin vs Standard of Care: deaths from any cause. Trial comparisons, record NCT02208063-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02208063-deaths

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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 10.05170.01770.141wilson
Risk in group 20.08330.03610.181wilson
Risk difference, group 1 minus group 2-0.0316-0.1350.0697newcombe hybrid score
Risk ratio, group 1 over group 20.6210.1552.48log
Odds ratio, group 1 over group 20.60.1372.63log
Number needed to treat, for one fewer death from any cause on Telavancin than on Standard of Care31.6from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: standard of care.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Telavancin7.5 mg/kg administered intravenously once every 24 hours daily over 60 minutes~Telavancin358EG000
Group 2Standard of CareVancomycin, Daptomycin, synthetic penicillin or Cefazolin~Vancomycin~Daptomycin~Synthetic penicillin~Cefazolin560EG001

Harm

What it counts
Total, all-cause mortality
Time frame
38 months

Source ClinicalTrials.gov

Trial

Title
A Phase 3 Telavancin Staphylococcus Aureus (S. Aureus) Bacteremia Trial
NCT number
NCT02208063
Phases
PHASE3
Conditions
Bacteremia
Interventions
Telavancin, Vancomycin, Daptomycin, Synthetic penicillin, Cefazolin
Lead sponsor
Cumberland Pharmaceuticals
Results first posted
2020-02-17

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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