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Trial · NCT02048722

Results by group95

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

OutcomeGroupCategoryValueSpreadUnits
Progression-Free Survival (PFS) at 4 MonthsTreatment (Regorafenib)52.1795% Confidence Interval 35.28 to 77.16percentage of patients alive
Progression-Free Survival (PFS) at 3 and 6 MonthsTreatment (Regorafenib)3 months56.5295% Confidence Interval 39.5 to 80.89percentage patients alive
Progression-Free Survival (PFS) at 3 and 6 MonthsTreatment (Regorafenib)6 months47.8395% Confidence Interval 31.21 to 73.29percentage patients alive
Median Progression-free Survival (PFS)Treatment (Regorafenib)5.4995% Confidence Interval 1.84 to 9.53months
Overall SurvivalTreatment (Regorafenib)14.0695% Confidence Interval 9.76 to 22.24months
Response RateTreatment (Regorafenib)Complete Response2participants
Response RateTreatment (Regorafenib)Partial Response2participants
Rate of Tumor ControlTreatment (Regorafenib)Complete Response2patients
Rate of Tumor ControlTreatment (Regorafenib)Partial Response2patients
Rate of Tumor ControlTreatment (Regorafenib)Stable Disease9patients
Number of Grade 1, 2, 3, 4, and 5 Related Adverse Events Observed During Study Treatment (Defined by CTCAE v 4.0)Treatment (Regorafenib)Blood and lymphatic system disorders / Grade 15Participants
Number of Grade 1, 2, 3, 4, and 5 Related Adverse Events Observed During Study Treatment (Defined by CTCAE v 4.0)Treatment (Regorafenib)Blood and lymphatic system disorders / Grade 23Participants
Number of Grade 1, 2, 3, 4, and 5 Related Adverse Events Observed During Study Treatment (Defined by CTCAE v 4.0)Treatment (Regorafenib)Blood and lymphatic system disorders / Grade 33Participants
Number of Grade 1, 2, 3, 4, and 5 Related Adverse Events Observed During Study Treatment (Defined by CTCAE v 4.0)Treatment (Regorafenib)Blood and lymphatic system disorders / Grade 40Participants
Number of Grade 1, 2, 3, 4, and 5 Related Adverse Events Observed During Study Treatment (Defined by CTCAE v 4.0)Treatment (Regorafenib)Blood and lymphatic system disorders / Number of patients who didn't experience any grade20Participants
Number of Grade 1, 2, 3, 4, and 5 Related Adverse Events Observed During Study Treatment (Defined by CTCAE v 4.0)Treatment (Regorafenib)Endocrine disorders / Grade 11Participants
Number of Grade 1, 2, 3, 4, and 5 Related Adverse Events Observed During Study Treatment (Defined by CTCAE v 4.0)Treatment (Regorafenib)Endocrine disorders / Grade 20Participants
Number of Grade 1, 2, 3, 4, and 5 Related Adverse Events Observed During Study Treatment (Defined by CTCAE v 4.0)Treatment (Regorafenib)Endocrine disorders / Grade 30Participants
Number of Grade 1, 2, 3, 4, and 5 Related Adverse Events Observed During Study Treatment (Defined by CTCAE v 4.0)Treatment (Regorafenib)Endocrine disorders / Grade 40Participants
Number of Grade 1, 2, 3, 4, and 5 Related Adverse Events Observed During Study Treatment (Defined by CTCAE v 4.0)Treatment (Regorafenib)Endocrine disorders / Number of patients who didn't experience any grade30Participants

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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