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Trial · NCT02175654

Registered outcomes19

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryProgression free survival rate at 6 months6 months
SecondaryObjective response rate based on the Response Evaluation Criteria in Solid Tumors criteria36 months
SecondaryDisease control rate36 months
SecondaryResponse according other criteria (Appendix 9)36 months
SecondaryTime to response36 months
SecondaryProgression free survival36 months
SecondaryTime to treatment failure36 months
SecondaryResponse duration36 months
SecondaryDuration of stable disease36 months
SecondaryOverall survival36 months
SecondaryTime to progression36 months
SecondaryIncidence and severity of adverse events (AE) (NCI CTC, version 3.0)36 months
SecondaryChanges in laboratory valuesbaseline and end of treatment, an expected average of 4 months
hemoglobin, hematocrit, platelets, creatinine, total bilirubin, alkaline phosphatase, ALT, AST, BUN or urea, glucose, sodium, potassium, calcium, phosphorus, LDH, GGT, magnesium, albumin, total protein, uric acid and lipase.
SecondaryChange in vital signs (weight loss and hypertension)baseline and end of treatment, an expected average of 4 months
SecondaryIncidence of dose adjustments and compliance36 months
SecondaryIncidence of concomitant medication36 months
SecondaryChanges in ECOG performance status over time from baselinebaseline and end of treatment, an expected average of 4 months
OthermicroRNA expression level in the Peripheral Blood36 months
OtherBiomarkers associated with cell and tumour growth and/or the mechanism of action of regorafenib and their correlation with patients' clinical progression for efficacy and safety parameters.36 months

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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