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Comparison · NCT01706458-b16e8fe8

Sipuleucel-T vs Sipuleucel-T With DNA Vaccine: Progression-free Survival

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. Sipuleucel-T vs Sipuleucel-T With DNA Vaccine: Progression-free Survival. Trial comparisons, record NCT01706458-b16e8fe8. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01706458-b16e8fe8

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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 1000.299wilson
Risk in group 2000.299wilson
Risk difference, group 1 minus group 20-0.2990.299newcombe hybrid score
Risk ratio, group 1 over group 2loga group has no participants with the outcome
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to treatfrom the risk difference intervalthe two groups' risks are equal

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Sipuleucel-TPatients receive sipuleucel-T IV on weeks 0, 2, and 4.~sipuleucel-T: Given IV09OG000
Group 2Sipuleucel-T With DNA VaccinePatients receive sipuleucel-T as patients in arm I and pTVG-HP plasmid DNA vaccine ID on weeks 6, 8, 10, and 12, and then at 6 and 9 months.~sipuleucel-T: Given IV~DNA Vaccine: Given ID09OG001

Outcome

Type
SECONDARY
Title
Progression-free Survival
Description
Percentage of patients without radiographic progression at 12 months.
Time frame
12 months
Population

Source ClinicalTrials.gov

Trial

Title
Provenge With or Without pTVG-HP DNA Booster Vaccine in Prostate Cancer
NCT number
NCT01706458
Phases
PHASE2
Conditions
Prostate Cancer
Interventions
sipuleucel-T, DNA Vaccine
Lead sponsor
University of Wisconsin, Madison
Results first posted
2018-07-17

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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