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Trial · NCT02015065

Results by group25

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

OutcomeGroupCategoryValueSpreadUnits
Number of Participants With a Clinical Activity-radiographic Response200 mg Vandetanib AdultComplete Response0Participants
Number of Participants With a Clinical Activity-radiographic Response300 mg Vandetanib AdultComplete Response0Participants
Number of Participants With a Clinical Activity-radiographic ResponseDose Level 100mg/m^2 Vandetanib PediatricComplete Response0Participants
Number of Participants With a Clinical Activity-radiographic Response200 mg Vandetanib AdultPartial Response0Participants
Number of Participants With a Clinical Activity-radiographic Response300 mg Vandetanib AdultPartial Response0Participants
Number of Participants With a Clinical Activity-radiographic ResponseDose Level 100mg/m^2 Vandetanib PediatricPartial Response0Participants
Number of Participants With a Clinical Activity-radiographic Response200 mg Vandetanib AdultStable Disease1Participants
Number of Participants With a Clinical Activity-radiographic Response300 mg Vandetanib AdultStable Disease2Participants
Number of Participants With a Clinical Activity-radiographic ResponseDose Level 100mg/m^2 Vandetanib PediatricStable Disease1Participants
Number of Participants With a Clinical Activity-radiographic Response200 mg Vandetanib AdultProgressive Disease1Participants
Number of Participants With a Clinical Activity-radiographic Response300 mg Vandetanib AdultProgressive Disease3Participants
Number of Participants With a Clinical Activity-radiographic ResponseDose Level 100mg/m^2 Vandetanib PediatricProgressive Disease1Participants
Count of Participants With Serious and Non-serious Adverse Events200 mg Vandetanib Adult2Participants
Count of Participants With Serious and Non-serious Adverse Events300 mg Vandetanib Adult5Participants
Count of Participants With Serious and Non-serious Adverse EventsDose Level 100mg/m^2 Vandetanib Pediatric2Participants
Percentage of Participants Overall Survival200 mg Vandetanib Adult5095% Confidence Interval 0.6 to 91percentage of participants
Percentage of Participants Overall Survival300 mg Vandetanib Adult6095% Confidence Interval 12.6 to 88.2percentage of participants
Percentage of Participants Overall SurvivalDose Level 100mg/m^2 Vandetanib Pediatric5095% Confidence Interval 0.6 to 91percentage of participants
Progression Free-Survival200 mg Vandetanib Adult495% Confidence Interval 0.6 to 91Months
Progression Free-Survival300 mg Vandetanib Adult5.195% Confidence Interval 1.8 to 22.5Months

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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