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Comparison · NCT00537095-6493d314

ZD6474 vs PLACEBO: Time to Death

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. ZD6474 vs PLACEBO: Time to Death. Trial comparisons, record NCT00537095-6493d314. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00537095-6493d314

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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 10.2640.1760.376wilson
Risk in group 20.2880.1970.4wilson
Risk difference, group 1 minus group 2-0.0238-0.1660.121newcombe hybrid score
Risk ratio, group 1 over group 20.9170.5411.56log
Odds ratio, group 1 over group 20.8880.4281.84log
Number needed to treat, for one fewer participant with the outcome on ZD6474 than on PLACEBO42from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1ZD6474ZD6474, Vandetanib 300mg1972OG000
Group 2PLACEBOPLACEBO2173OG001

Outcome

Type
SECONDARY
Title
Time to Death
Description
Interim analysis time to date of randomization to date of death (data not mature at the time of this analysis, so number of deaths displayed instead.
Time frame
time from randomization to date of death
Population
For the efficacy part, 72 were randomized to received ZD6474 and 73 placebo. For the safety part, 73 patients received at least one dose of ZD6474 and 72 placebo

Source ClinicalTrials.gov

Trial

Title
Efficacy and Safety of Vandetanib (ZD6474) in Patients With Metastatic Papillary or Follicular Thyroid Cancer
NCT number
NCT00537095
Phases
PHASE2
Conditions
Thyroid Neoplasms
Interventions
Vandetanib, Placebo
Lead sponsor
Genzyme, a Sanofi Company
Results first posted
2011-07-08

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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