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Trial · NCT00872989

Results by group178

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Progression Free Survival (PFS)Arm I: Docetaxel3.595% Confidence Interval 2.3 to 4.6months
Progression Free Survival (PFS)Arm II: Docetaxel + Vandetanib3.095% Confidence Interval 1.6 to 4.3months
Number of Participants With a Complete Response, Partial Response, Stable Disease, or Increasing DiseaseArm I: DocetaxelComplete Response0participants
Number of Participants With a Complete Response, Partial Response, Stable Disease, or Increasing DiseaseArm II: Docetaxel + VandetanibComplete Response0participants
Number of Participants With a Complete Response, Partial Response, Stable Disease, or Increasing DiseaseArm I: DocetaxelPartial Response5participants
Number of Participants With a Complete Response, Partial Response, Stable Disease, or Increasing DiseaseArm II: Docetaxel + VandetanibPartial Response6participants
Number of Participants With a Complete Response, Partial Response, Stable Disease, or Increasing DiseaseArm I: DocetaxelUnconfirmed Complete Response1participants
Number of Participants With a Complete Response, Partial Response, Stable Disease, or Increasing DiseaseArm II: Docetaxel + VandetanibUnconfirmed Complete Response0participants
Number of Participants With a Complete Response, Partial Response, Stable Disease, or Increasing DiseaseArm I: DocetaxelUnconfirmed Partial Response2participants
Number of Participants With a Complete Response, Partial Response, Stable Disease, or Increasing DiseaseArm II: Docetaxel + VandetanibUnconfirmed Partial Response2participants
Number of Participants With a Complete Response, Partial Response, Stable Disease, or Increasing DiseaseArm I: DocetaxelStable/No Response19participants
Number of Participants With a Complete Response, Partial Response, Stable Disease, or Increasing DiseaseArm II: Docetaxel + VandetanibStable/No Response17participants
Number of Participants With a Complete Response, Partial Response, Stable Disease, or Increasing DiseaseArm I: DocetaxelIncreasing Disease23participants
Number of Participants With a Complete Response, Partial Response, Stable Disease, or Increasing DiseaseArm II: Docetaxel + VandetanibIncreasing Disease20participants
Number of Participants With a Complete Response, Partial Response, Stable Disease, or Increasing DiseaseArm I: DocetaxelSymptomatic Deterioration0participants
Number of Participants With a Complete Response, Partial Response, Stable Disease, or Increasing DiseaseArm II: Docetaxel + VandetanibSymptomatic Deterioration1participants
Number of Participants With a Complete Response, Partial Response, Stable Disease, or Increasing DiseaseArm I: DocetaxelAssessment Inadequate7participants
Number of Participants With a Complete Response, Partial Response, Stable Disease, or Increasing DiseaseArm II: Docetaxel + VandetanibAssessment Inadequate6participants
Overall SurvivalArm I: Docetaxel1895% Confidence Interval 13.7 to 26.1months
Overall SurvivalArm II: Docetaxel + Vandetanib1495% Confidence Interval 9.9 to 19.7months

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
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
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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