NCT00543543 · OUTCOME
Base Study: Combined Incidence of HPV Type 31/33/45/52/58-related Persistent Infection
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- NUMBER
- Unit
- Cases per 10,000 person-years follow-up
- Interval / dispersion
- Not reported
- Time frame
- Up to Month 54 in the base study
What was measured
Combined Incidence of HPV Type 31/33/45/52/58-related persistent infection as determined by clinical/pathologic criteria and positive Polymerase Chain Reaction (PCR) assay for virus subtype. Persistent infection was defined as infection detected in samples from \>=2 consecutive visits 6 months (+/-1 month visit window) or longer apart. Incidence was defined as the number of cases of persistent infection per 10,000 person-years of follow-up in a treatment arm.
Analysis population: The Per-protocol Efficacy population included all participants who received all 3 vaccinations of mid-dose V503 or Gardasil within acceptable day ranges, were seronegative at Day 1 and PCR negative at Day 1 through Day 7 to the relevant HPV types, and had at least 1 follow-up visit following Month 7.
Groups in this outcome
Mid-dose V503
V503 (9-Valent HPV Vaccine) mid-dose 0.5 mL injection in a 3-dose regimen in the base study. A subset of participants (Cohort 1) received a fourth V503 mid-dose vaccination in the extension study.
Gardasil
Gardasil (4-Valent HPV Vaccine) 0.5 mL injection in a 3-dose regimen in the base study. Participants (Cohort 2) were offered the V503 mid-dose 3-dose regimen in the extension study.
| Group | Source count |
|---|---|
| Mid-dose V503 | 5941 |
| Gardasil | 5955 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Mid-dose V503 | 21.5 | Not reported | Not reported | Not reported | Not reported |
| Gardasil | 538.8 | Not reported | Not reported | Not reported | Not reported |
Source statistical analyses
- ci Lower Limit
- 94.6
- ci Num Sides
- TWO_SIDED
- ci Pct Value
- 95
- ci Upper Limit
- 97.1
- estimate Comment
- Vaccine efficacy = 100 \* \[1 - (incidence rate with V503 / incidence rate with Gardasil)\]. The pre-specified success criterion was a lower bound of the 95% confidence interval of observed efficacy of \>25%.
- group Ids
- OG000
- OG001
- non Inferiority Type
- SUPERIORITY_OR_OTHER
- param Type
- Vaccine efficacy
- param Value
- 96.0
Complete source fields
- analyses
- ci Lower Limit
- 94.6
- ci Num Sides
- TWO_SIDED
- ci Pct Value
- 95
- ci Upper Limit
- 97.1
- estimate Comment
- Vaccine efficacy = 100 \* \[1 - (incidence rate with V503 / incidence rate with Gardasil)\]. The pre-specified success criterion was a lower bound of the 95% confidence interval of observed efficacy of \>25%.
- group Ids
- OG000
- OG001
- non Inferiority Type
- SUPERIORITY_OR_OTHER
- param Type
- Vaccine efficacy
- param Value
- 96.0
- classes
- categories
- measurements
- group Id
- OG000
- value
- 21.5
- group Id
- OG001
- value
- 538.8
- denoms
- counts
- group Id
- OG000
- value
- 5941
- group Id
- OG001
- value
- 5955
- units
- Participants
- description
- Combined Incidence of HPV Type 31/33/45/52/58-related persistent infection as determined by clinical/pathologic criteria and positive Polymerase Chain Reaction (PCR) assay for virus subtype. Persistent infection was defined as infection detected in samples from \>=2 consecutive visits 6 months (+/-1 month visit window) or longer apart. Incidence was defined as the number of cases of persistent infection per 10,000 person-years of follow-up in a treatment arm.
- groups
- description
- V503 (9-Valent HPV Vaccine) mid-dose 0.5 mL injection in a 3-dose regimen in the base study. A subset of participants (Cohort 1) received a fourth V503 mid-dose vaccination in the extension study.
- id
- OG000
- title
- Mid-dose V503
- description
- Gardasil (4-Valent HPV Vaccine) 0.5 mL injection in a 3-dose regimen in the base study. Participants (Cohort 2) were offered the V503 mid-dose 3-dose regimen in the extension study.
- id
- OG001
- title
- Gardasil
- param Type
- NUMBER
- population Description
- The Per-protocol Efficacy population included all participants who received all 3 vaccinations of mid-dose V503 or Gardasil within acceptable day ranges, were seronegative at Day 1 and PCR negative at Day 1 through Day 7 to the relevant HPV types, and had at least 1 follow-up visit following Month 7.
- reporting Status
- POSTED
- time Frame
- Up to Month 54 in the base study
- title
- Base Study: Combined Incidence of HPV Type 31/33/45/52/58-related Persistent Infection
- type
- SECONDARY
- unit Of Measure
- Cases per 10,000 person-years follow-up
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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