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Trial · NCT03790111

Results by group37

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

OutcomeGroupCategoryValueSpreadUnits
Number of Participants With Progression-free Survival (PFS) as Evaluated by Central Radiologist's AssessmentXermelo 250mg Plus 1L Therapy for a Week, Then Xermelo 500mgSafety Population / Responders, Central Reviewer12Participants
Number of Participants With Progression-free Survival (PFS) as Evaluated by Central Radiologist's AssessmentXermelo 250mg Plus 1L Therapy for a Week, Then Xermelo 500mgSafety Population / Non-Responders, Central Reviewer41Participants
Number of Participants With Progression-free Survival (PFS) as Evaluated by Central Radiologist's AssessmentXermelo 250mg Plus 1L Therapy for a Week, Then Xermelo 500mgPer Protocol Population / Responders, Central Reviewer12Participants
Number of Participants With Progression-free Survival (PFS) as Evaluated by Central Radiologist's AssessmentXermelo 250mg Plus 1L Therapy for a Week, Then Xermelo 500mgPer Protocol Population / Non-Responders, Central Reviewer30Participants
Number of Participants With Progression-free Survival (PFS) as Evaluated by Central Radiologist's AssessmentXermelo 250mg Plus 1L Therapy for a Week, Then Xermelo 500mgBy Treatment Cycle Population / Responders, Central Reviewer12Participants
Number of Participants With Progression-free Survival (PFS) as Evaluated by Central Radiologist's AssessmentXermelo 250mg Plus 1L Therapy for a Week, Then Xermelo 500mgBy Treatment Cycle Population / Non-Responders, Central Reviewer21Participants
Project Overall Survival Rate at Month 6Xermelo 250mg Plus 1L Therapy for a Week, Then Xermelo 500mg0.8795% Confidence Interval 0.74 to 0.93Proportion of participants
Overall Survival (OS)Xermelo 250mg Plus 1L Therapy for a Week, Then Xermelo 500mg17.66795% Confidence Interval 11.567 to NAMonths
Project Overall Survival Rate at Month 12Xermelo 250mg Plus 1L Therapy for a Week, Then Xermelo 500mg0.6095% Confidence Interval 0.45 to 0.72Proportion of participants
Median Progression Free SurvivalXermelo 250mg Plus 1L Therapy for a Week, Then Xermelo 500mg6.23395% Confidence Interval 4.067 to 7.467Months
Disease Control Rate (DCR), Central Radiologist's AssessmentXermelo 250mg Plus 1L Therapy for a Week, Then Xermelo 500mg33Participants
Disease Control Rate (DCR), Central Radiologist's AssessmentXermelo 250mg Plus 1L Therapy for a Week, Then Xermelo 500mg33Participants
Disease Control Rate (DCR), Central Radiologist's AssessmentXermelo 250mg Plus 1L Therapy for a Week, Then Xermelo 500mg35Participants
Overall (Objective) Response Rate (ORR), Central Radiologist's AssessmentXermelo 250mg Plus 1L Therapy for a Week, Then Xermelo 500mg7Participants
Overall (Objective) Response Rate (ORR), Central Radiologist's AssessmentXermelo 250mg Plus 1L Therapy for a Week, Then Xermelo 500mg7Participants
Overall (Objective) Response Rate, Central Radiologist's AssessmentXermelo 250mg Plus 1L Therapy for a Week, Then Xermelo 500mg7Participants
Summary of Duration of Progression Free Survival, Local Radiologist's AssessmentXermelo 250mg Plus 1L Therapy for a Week, Then Xermelo 500mg7.00095% Confidence Interval 5.567 to NAMonths
Progression Free Survival, Local Radiologist's AssessmentXermelo 250mg Plus 1L Therapy for a Week, Then Xermelo 500mg7.46795% Confidence Interval 5.567 to 10.533Months
Progression Free Survival, Local Radiologist's AssessmentXermelo 250mg Plus 1L Therapy for a Week, Then Xermelo 500mg7.46795% Confidence Interval 5.567 to 10.533Months
Overall (Objective) Response Rate, Local ReadXermelo 250mg Plus 1L Therapy for a Week, Then Xermelo 500mg6Participants

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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