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Comparison · NCT01193257-3de665af

Placebo + Prednisone vs Orteronel + Prednisone: Number of Participants With Best Pain Response

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. Placebo + Prednisone vs Orteronel + Prednisone: Number of Participants With Best Pain Response. Trial comparisons, record NCT01193257-3de665af. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01193257-3de665af

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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 10.1970.160.241wilson
Risk in group 20.2260.1970.258wilson
Risk difference, group 1 minus group 2-0.0289-0.0780.0236newcombe hybrid score
Risk ratio, group 1 over group 20.8720.6821.12log
Odds ratio, group 1 over group 20.8410.6161.15log
Number needed to treat, for one fewer participant with the outcome on Placebo + Prednisone than on Orteronel + Prednisone34.6from 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 1Placebo + PrednisoneOrteronel placebo-matching tablets, orally, twice daily (BID) and prednisone 5 mg, tablets, orally, BID up to Day 28 of each treatment cycle throughout the study.72365OG000
Group 2Orteronel + Prednisone
Orteronel 400 mg, tablets, orally, BID and prednisone 5 mg, tablets, orally, BID up to Day 28 of each treatment cycle throughout the study. In Japan only, participants were administered with orteronel 300 mg, tablets, orally, BID and prednisone 5 mg, tablets, orally, BID up to Day 28 of each treatment cycle throughout the study.
166734OG001

Outcome

Type
SECONDARY
Title
Number of Participants With Best Pain Response
Description
Best pain response was evaluated in participants who had a pain response across the entire study were summarized by treatment group. The pain response was defined as a \>=2-point reduction from baseline in BPI-SF worst pain score without an increase in analgesic use, or a 25% or more reduction in analgesic use from baseline without an increase in worst pain score from baseline.
Time frame
Baseline until disease progression or death, whichever occurred first (approximately up to 4.5 years)
Population
ITT population included all participants who were randomized.

Source ClinicalTrials.gov

Trial

Title
Study Comparing Orteronel Plus Prednisone in Participants With Metastatic Castration-Resistant Prostate Cancer.
NCT number
NCT01193257
Phases
PHASE3
Conditions
Prostate Cancer
Interventions
Orteronel, Prednisone, Orteronel Placebo
Lead sponsor
Millennium Pharmaceuticals, Inc.
Results first posted
2018-12-19

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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