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Trial · NCT00923247

Results by group53

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

OutcomeGroupCategoryValueSpreadUnits
Phase I: Maximum Tolerated Dose (MTD) of Daily Oral VandetanibPhase 1300mg
Phase I: Maximum Tolerated Dose (MTD) of Daily Oral BortezomibPhase 11.3mg/m^2
Phase 2: Tumor Response in Adults With a Diagnosis of Medullary Thyroid Cancer (MTC) Treated With Daily Oral Vandetanib and BortezomibPhase 2 AComplete Response0Participants
Phase 2: Tumor Response in Adults With a Diagnosis of Medullary Thyroid Cancer (MTC) Treated With Daily Oral Vandetanib and BortezomibPhase 2 APartial Response0Participants
Phase 2: Tumor Response in Adults With a Diagnosis of Medullary Thyroid Cancer (MTC) Treated With Daily Oral Vandetanib and BortezomibPhase 2 AStable Disease0Participants
Phase 2: Tumor Response in Adults With a Diagnosis of Medullary Thyroid Cancer (MTC) Treated With Daily Oral Vandetanib and BortezomibPhase 2 AProgressive Disease1Participants
Phase 2: Progression Free Survival in Adults With a Diagnosis of Medullary Thyroid Cancer (MTC) Treated With Daily Oral Vandetanib and BortezomibPhase 2 A - Vandetanib and Bortezomib at the MTD3.67months
Response Rate (Complete Response (CR) + Partial Response (PR) of Adults With a Diagnosis of MTC Treated With Either of Two Regimens: (1) Daily Oral Vandetanib and Bortezomib or (2) Daily Oral Vandetanib
Phase 1Complete Response0Participants
Response Rate (Complete Response (CR) + Partial Response (PR) of Adults With a Diagnosis of MTC Treated With Either of Two Regimens: (1) Daily Oral Vandetanib and Bortezomib or (2) Daily Oral Vandetanib
Phase 2AComplete Response0Participants
Response Rate (Complete Response (CR) + Partial Response (PR) of Adults With a Diagnosis of MTC Treated With Either of Two Regimens: (1) Daily Oral Vandetanib and Bortezomib or (2) Daily Oral Vandetanib
Phase 1Partial Response6Participants
Response Rate (Complete Response (CR) + Partial Response (PR) of Adults With a Diagnosis of MTC Treated With Either of Two Regimens: (1) Daily Oral Vandetanib and Bortezomib or (2) Daily Oral Vandetanib
Phase 2APartial Response0Participants
Progression Free Survival (PFS)Phase 130.2Full Range 1.8 to 93.67Months
Progression Free Survival (PFS)Phase 2A3.02Months
Number of Participants With Adverse EventsPhase 121Participants
Number of Participants With Adverse EventsPhase 2 A0Participants
Number of Participants With Tumor Biomarker Calcitonin (CTN) ResponsePhase 1Complete response0Participants
Number of Participants With Tumor Biomarker Calcitonin (CTN) ResponsePhase 2AComplete response0Participants
Number of Participants With Tumor Biomarker Calcitonin (CTN) ResponsePhase 1Partial response5Participants
Number of Participants With Tumor Biomarker Calcitonin (CTN) ResponsePhase 2APartial response0Participants
Number of Participants With Tumor Biomarker Calcitonin (CTN) ResponsePhase 1Stable disease6Participants

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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