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Comparison · NCT01799993-c2a168f8

Amikacin Inhale (BAY41-6551) vs Placebo: Number of Participants With Emergence of New Respiratory Pathogens During the Aerosol Treatment Period

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. Amikacin Inhale (BAY41-6551) vs Placebo: Number of Participants With Emergence of New Respiratory Pathogens During the Aerosol Treatment Period. Trial comparisons, record NCT01799993-c2a168f8. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01799993-c2a168f8

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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 10.08240.05450.123wilson
Risk in group 20.1340.09780.182wilson
Risk difference, group 1 minus group 2-0.052-0.1070.00237newcombe hybrid score
Risk ratio, group 1 over group 20.6130.3661.03log
Odds ratio, group 1 over group 20.5780.3251.03log
Number needed to treat, for one fewer participant with the outcome on Amikacin Inhale (BAY41-6551) than on Placebo19.2from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Amikacin Inhale (BAY41-6551)Participants received 400 mg (3.2 mL) aerosolized Amikacin (BAY41-6551) solution every 12 hours via Pulmonary Drug Delivery System (PDDS) Clinical from Day 1 to Day 10.21255OG000
Group 2PlaceboParticipants received 3.2 mL aerosolized placebo solution every 12 hours via PDDS Clinical from Day 1 to Day 10.34253OG001

Outcome

Type
OTHER_PRE_SPECIFIED
Title
Number of Participants With Emergence of New Respiratory Pathogens During the Aerosol Treatment Period
Description
New pathogens also denoted as superinfection was defined as the isolation of a new pathogen (not the original baseline pathogen) from a specimen taken while the participant was on antibiotic therapy (Day 1 to EOT) and having a need for alternative antimicrobial therapy. Rates of emergence of any new pathogen by participant after start of study drug were summarized for each treatment group.
Time frame
Up to 10 days after start of study treatment
Population
mITT population

Source ClinicalTrials.gov

Trial

Title
Inhaled Amikacin Solution BAY41-6551 as Adjunctive Therapy in the Treatment of Gram-Negative Pneumonia
NCT number
NCT01799993
Phases
PHASE3
Conditions
Pneumonia, Bacterial
Interventions
Amikacin Inhalation Solution (BAY41-6551), Aerosolized Placebo
Lead sponsor
Bayer
Results first posted
2018-06-26

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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