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Comparison · NCT01651949-sae

Heterosexual and MSM Males vs Females: 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. Heterosexual and MSM Males vs Females: serious adverse events. Trial comparisons, record NCT01651949-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01651949-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 10.01650.0110.0246wilson
Risk in group 20.02420.01660.0352wilson
Risk difference, group 1 minus group 2-0.00769-0.020.00347newcombe hybrid score
Risk ratio, group 1 over group 20.6820.3911.19log
Odds ratio, group 1 over group 20.6770.3841.19log
Number needed to treat, for one fewer participant with a serious adverse event on Heterosexual and MSM Males than on Females130from the risk difference intervalthe interval includes no difference

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Heterosexual and MSM MalesHealthy heterosexual and MSM males 16 to 26 years of age received 9vHPV vaccine 0.5 mL intramuscular injection on Day 1, Month 1, and Month 6231,394EG000
Group 2FemalesHealthy females 16 to 26 years of age received 9vHPV vaccine 0.5 mL intramuscular injection on Day 1, Month 1, and Month 6261,075EG001

Harm

What it counts
Total, serious adverse events
Time frame
Up to Month 12

Source ClinicalTrials.gov

Trial

Title
Multivalent HPV (Human Papillomavirus) Vaccine Study in 16- to 26-Year Old Men and Women (V503-003)
NCT number
NCT01651949
Phases
PHASE3
Conditions
Genital Warts, Anal Cancer, Anal Intraepithelial Neoplasia
Interventions
9vHPV Vaccine
Lead sponsor
Merck Sharp & Dohme LLC
Results first posted
2015-03-09

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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