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Comparison · NCT02878330-sae

MEDI8897 50 mg vs Placebo: serious adverse events

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. MEDI8897 50 mg vs Placebo: serious adverse events. Trial comparisons, record NCT02878330-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02878330-sae

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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 10.1120.09330.133wilson
Risk in group 20.1690.1380.205wilson
Risk difference, group 1 minus group 2-0.0575-0.0981-0.0199newcombe hybrid score
Risk ratio, group 1 over group 20.660.5050.861log
Odds ratio, group 1 over group 20.6170.4520.843log
Number needed to treat, for one fewer participant with a serious adverse event on MEDI8897 50 mg than on Placebo17.410.250.1from the risk difference interval

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1MEDI8897 50 mgParticipants received a single IM dose of MEDI8897 50 milligrams (mg) on Day 1 of the study.108968EG001
Group 2PlaceboParticipants received a single intramuscular (IM) dose of placebo matched to MEDI8897 on Day 1 of the study.81479EG000

Harm

What it counts
Total, serious adverse events
Time frame
From Day 1 through Day 361

Source ClinicalTrials.gov

Trial

Title
A Study to Evaluate the Safety and Efficacy of MEDI8897 for the Prevention of Medically Attended RSV LRTI in Healthy Preterm Infants.
NCT number
NCT02878330
Phases
PHASE2
Conditions
Respiratory Syncytial Virus Infections
Interventions
MEDI8897, Placebo
Lead sponsor
MedImmune LLC
Results first posted
2019-10-14

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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