ConductScience.org, home

Comparison · NCT00626548-451638a4

ZD4054 vs Placebo: Overall Survival

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

Download JSON
Cite this record

ConductScience Library. ZD4054 vs Placebo: Overall Survival. Trial comparisons, record NCT00626548-451638a4. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00626548-451638a4

On this page

Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.06760.050.0907wilson
Risk in group 20.06620.04880.0892wilson
Risk difference, group 1 minus group 20.00135-0.02760.0303newcombe hybrid score
Risk ratio, group 1 over group 21.020.6661.56log
Odds ratio, group 1 over group 21.020.6471.61log
Number needed to treat, for one more participant with the outcome on ZD4054 than on Placebo739from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1ZD4054ZD4054 10 mg oral tablet once daily40592OG000
Group 2PlaceboPlacebo oral tablet once daily39589OG001

Outcome

Type
PRIMARY
Title
Overall Survival
Description
Number of participants who have died at early analysis data cut off (DCO)
Time frame
From date of randomization until date of death, assessed up to 33 months
Population
The analysis population only includes patients recruited by the time of the early analysis (1 October 2010)

Source ClinicalTrials.gov

Trial

Title
A Phase III Trial of ZD4054 (Zibotentan) (Endothelin A Antagonist) in Non-metastatic Hormone Resistant Prostate Cancer
NCT number
NCT00626548
Phases
PHASE3
Conditions
Prostate Cancer
Interventions
ZD4054, Palcebo
Lead sponsor
AstraZeneca
Results first posted
2012-06-01

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.

For software

Read this comparison from software.

The record is JSON. No key.

GET https://conductscience.org/api/comparisons/v1/NCT00626548-451638a4