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Trial · NCT03375320

Results by group16

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

OutcomeGroupCategoryValueSpreadUnits
Progression-free Survival (PFS)Arm Ia (Cabozantinib S-malate, Extra-pancreatic NET Cohort [epNET])8.495% Confidence Interval 7.6 to 12.7months
Progression-free Survival (PFS)Arm IIa (Placebo, Extra-pancreatic NET Cohort [epNET])3.995% Confidence Interval 3.0 to 5.7months
Progression-free Survival (PFS)Arm Ib (Cabozantinib S-malate, Pancreatic NET Cohort [pNET])13.895% Confidence Interval 9.2 to 18.5months
Progression-free Survival (PFS)Arm IIb (Placebo, Pancreatic NET Cohort [pNET])4.495% Confidence Interval 3.0 to 5.9months
Overall Survival (OS)Arm Ia (Cabozantinib S-malate, Extra-pancreatic NET Cohort [epNET])21.995% Confidence Interval 18.8 to 30.4months
Overall Survival (OS)Arm IIa (Placebo, Extra-pancreatic NET Cohort [epNET])19.795% Confidence Interval 14.2 to 30.0months
Overall Survival (OS)Arm Ib (Cabozantinib S-malate, Pancreatic NET Cohort [pNET])40.095% Confidence Interval 31.3 to NAmonths
Overall Survival (OS)Arm IIb (Placebo, Pancreatic NET Cohort [pNET])31.195% Confidence Interval 23.4 to NAmonths
Number of Patients Experiencing Grade 3+ Adverse Events (AEs) Graded According to the Common Terminology Criteria for Adverse Events (CTCAE) and Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)
Arm Ia (Cabozantinib S-malate, Extra-pancreatic NET Cohort [epNET])104Participants
Number of Patients Experiencing Grade 3+ Adverse Events (AEs) Graded According to the Common Terminology Criteria for Adverse Events (CTCAE) and Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)
Arm IIa (Placebo, Extra-pancreatic NET Cohort [epNET])47Participants
Number of Patients Experiencing Grade 3+ Adverse Events (AEs) Graded According to the Common Terminology Criteria for Adverse Events (CTCAE) and Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)
Arm Ib (Cabozantinib S-malate, Pancreatic NET Cohort [pNET])49Participants
Number of Patients Experiencing Grade 3+ Adverse Events (AEs) Graded According to the Common Terminology Criteria for Adverse Events (CTCAE) and Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)
Arm IIb (Placebo, Pancreatic NET Cohort [pNET])22Participants
Radiographic Response RateArm Ia (Cabozantinib S-malate, Extra-pancreatic NET Cohort [epNET])7Participants
Radiographic Response RateArm IIa (Placebo, Extra-pancreatic NET Cohort [epNET])0Participants
Radiographic Response RateArm Ib (Cabozantinib S-malate, Pancreatic NET Cohort [pNET])12Participants
Radiographic Response RateArm IIb (Placebo, Pancreatic NET Cohort [pNET])0Participants

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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