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Trial · NCT03406871

Results by group11

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

OutcomeGroupCategoryValueSpreadUnits
The Number of Dose Limiting Toxicity (DLT) for RD DeterminationDose Escalation Cohort Regorafenib 80mg0Participants
The Number of Dose Limiting Toxicity (DLT) for RD DeterminationDose Escalation Cohort Regorafenib 120mg0Participants
The Number of Dose Limiting Toxicity (DLT) for RD DeterminationDose Escalation Cohort Regorafenib 160mg3Participants
The Number of Dose Limiting Toxicity (DLT) for RD DeterminationExpansion Cohort : Regorafenib 120mg5Participants
Objective Response Rate (ORR)Final Analysis42.095% Confidence Interval 28.2 to 56.8percentage of participants
Progression-Free Survival(PFS)Final Analysis6.395% Confidence Interval 3.9 to 10.4months
Overall Survival(OS)Final Analysis14.495% Confidence Interval 9.8 to 21.7median of months
Disease Control Rate(DCR)Final Analysis86.095% Confidence Interval 73.3 to 94.2percentage of participants
Adverse-EventsFinal Analysis: Regorafenib 80mg22Participants
Adverse-EventsFinal Analysis: Regorafenib 120mg25Participants
Adverse-EventsFinal Analysis: Regorafenib 160mg3Participants

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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