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Trial · NCT03011372

Results by group17

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

OutcomeGroupCategoryValueSpreadUnits
Percentage of Participants Who Achieved Complete Response (CR) as Determined by Investigator Assessment According to the Response Criteria for Myeloid/Lymphoid Neoplasms With FGFR1 RearrangementPemigatinib 13.5 mg68.995% Confidence Interval 53.35 to 81.83percentage of participants
Percentage of Participants Who Achieved CR as Determined by Central Review Committee (CRC) AssessmentPemigatinib 13.5 mg68.995% Confidence Interval 53.35 to 81.83percentage of participants
Percentage of Participants Who Achieved a Best Overall Response of Complete Response (CR) or Partial Response (PR) as Determined by Investigator Assessment According to the Response Criteria for Myeloid/Lymphoid Neoplasms With FGFR1 Rearrangement
Pemigatinib 13.5 mg77.895% Confidence Interval 62.91 to 88.80percentage of participants
Percentage of Participants Who Achieved a Best Overall Response of CR or PR as Determined by CRC AssessmentPemigatinib 13.5 mg75.695% Confidence Interval 60.46 to 87.12percentage of participants
Percentage of Participants Who Achieved a Complete Cytogenetic Response (CCyR) as Assessed by Local Analysis and Investigator EvaluationPemigatinib 13.5 mg73.395% Confidence Interval 58.06 to 85.40percentage of participants
Percentage of Participants Who Achieved a CCyR as Assessed by CRC AssessmentPemigatinib 13.5 mg73.395% Confidence Interval 58.06 to 85.40percentage of participants
Percentage of Participants Who Achieved a Partial Cytogenetic Response (PCyR) as Assessed by Local Analysis and Investigator EvaluationPemigatinib 13.5 mg8.995% Confidence Interval 2.48 to 21.22percentage of participants
Percentage of Participants Who Achieved a PCyR as Assessed by CRC AssessmentPemigatinib 13.5 mg15.695% Confidence Interval 6.49 to 29.46percentage of participants
Duration of Complete ResponsePemigatinib 13.5 mgInvestigator assessment53.2995% Confidence Interval 12.22 to NAmonths
Duration of Complete ResponsePemigatinib 13.5 mgCRC assessmentNA95% Confidence Interval 27.86 to NAmonths
Duration of ResponsePemigatinib 13.5 mgInvestigator assessment53.2995% Confidence Interval 15.51 to NAmonths
Duration of ResponsePemigatinib 13.5 mgCRC assessmentNA95% Confidence Interval 27.86 to NAmonths
Progression-free Survival (PFS)Pemigatinib 13.5 mgInvestigator assessment73.8995% Confidence Interval 54.74 to NAmonths
Progression-free Survival (PFS)Pemigatinib 13.5 mgCRC assessment73.8995% Confidence Interval 29.17 to NAmonths
Overall SurvivalPemigatinib 13.5 mgNA95% Confidence Interval 54.74 to NAmonths
Number of Participants With Any Treatment-emergent Adverse Event (TEAE)Pemigatinib 13.5 mg47Participants
Number of Participants With Any ≥Grade 3 TEAEPemigatinib 13.5 mg39Participants

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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