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Trial · NCT02075840

Results by group374

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

OutcomeGroupCategoryValueSpreadUnits
Progression-Free Survival (PFS) by Investigator AssessmentAlectinibNA95% Confidence Interval 17.7 to NAmonths
Progression-Free Survival (PFS) by Investigator AssessmentCrizotinib11.195% Confidence Interval 9.1 to 13.1months
Percentage of Participants With PFS Event by Investigator AssessmentAlectinib40.8Percentage of Participants
Percentage of Participants With PFS Event by Investigator AssessmentCrizotinib67.5Percentage of Participants
PFS Independent Review Committee (IRC)-AssessedAlectinib25.795% Confidence Interval 19.9 to NAmonths
PFS Independent Review Committee (IRC)-AssessedCrizotinib10.495% Confidence Interval 7.7 to 14.6months
Percentage of Participants With PFS Event by IRCAlectinib41.4Percentage of Participants
Percentage of Participants With PFS Event by IRCCrizotinib60.9Percentage of Participants
Percentage of Participants With Central Nervous System (CNS) Progression as Determined by IRC Using RECIST V1.1 CriteriaAlectinib11.8Percentage of Participants
Percentage of Participants With Central Nervous System (CNS) Progression as Determined by IRC Using RECIST V1.1 CriteriaCrizotinib45.0Percentage of Participants
Percentage of Participants With Central Nervous System (CNS) Progression as Determined by IRC Using Revised Assessment in Neuro Oncology (RANO) CriteriaAlectinib10.5Percentage of Participants
Percentage of Participants With Central Nervous System (CNS) Progression as Determined by IRC Using Revised Assessment in Neuro Oncology (RANO) CriteriaCrizotinib35.8Percentage of Participants
Percentage of Participants With Objective Response Rate (ORR) of Complete Response (CR) or Partial Response (PR) as Determined by The Investigators According to RECIST V1.1 CriteriaAlectinib82.995% Confidence Interval 75.95 to 88.51Percentage of Participants
Percentage of Participants With Objective Response Rate (ORR) of Complete Response (CR) or Partial Response (PR) as Determined by The Investigators According to RECIST V1.1 CriteriaCrizotinib75.595% Confidence Interval 67.84 to 82.12Percentage of Participants
Duration of Response (DOR) According to RECIST V1.1 Criteria as Assessed by the InvestigatorsAlectinibNA95% Confidence Interval NA to NAMonths
Duration of Response (DOR) According to RECIST V1.1 Criteria as Assessed by the InvestigatorsCrizotinib11.195% Confidence Interval 7.9 to 13.0Months
Overall Survival (OS)AlectinibNA95% Confidence Interval NA to NAmonths
Overall Survival (OS)CrizotinibNA95% Confidence Interval NA to NAmonths
Percentage of Participants With OS EventAlectinib23.0Percentage of Participants
Percentage of Participants With OS EventCrizotinib26.5Percentage of Participants

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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