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Comparison · NCT00617669-sae

ZD4054 + Docetaxel vs Placebo + Docetaxel: 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. ZD4054 + Docetaxel vs Placebo + Docetaxel: serious adverse events. Trial comparisons, record NCT00617669-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00617669-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 10.410.3690.453wilson
Risk in group 20.3870.3460.429wilson
Risk difference, group 1 minus group 20.0233-0.03590.0823newcombe hybrid score
Risk ratio, group 1 over group 21.060.9131.23log
Odds ratio, group 1 over group 21.10.861.41log
Number needed to harm, for one more participant with a serious adverse event on ZD4054 + Docetaxel than on Placebo + Docetaxel42.9from 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 1ZD4054 + DocetaxelXD4054 10 mg oral tablet once daily + docetaxel intravenous infusion every 3 weeks214522EG000
Group 2Placebo + Docetaxelplacebo oral tablet once daily + docetaxel intravenous infusion every 3 weeks203525EG001

Harm

What it counts
Total, serious adverse events
Time frame

Source ClinicalTrials.gov

Trial

Title
A Phase III Trial of ZD4054 (Zibotentan) (Endothelin A Antagonist) and Docetaxel in Metastatic Hormone Resistant Prostate Cancer
NCT number
NCT00617669
Phases
PHASE3
Conditions
Prostate Cancer
Interventions
Docetaxel, ZD4054, Placebo
Lead sponsor
AstraZeneca
Results first posted
2012-05-31

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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