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Trial · NCT01093573

Results by group12

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

OutcomeGroupCategoryValueSpreadUnits
Maximum Tolerated Dose of Midostaurin in Combination With Azacitidine in Patients With Acute Myelogenous Leukemia (Phase I)Midostaurin Dose Escalation75mg/bid
Number of Participants With Hematologic Improvement (Phase I)Dose Level 10Participants
Number of Participants With Hematologic Improvement (Phase I)Dose Level 20Participants
Number of Participants With Hematologic Improvement (Phase I)Dose Level 32Participants
Overall Response Rate (Phase II)Dose Level 3Complete Remission (CR)4Participants
Overall Response Rate (Phase II)Dose Level 3Complete Remission with incomplete recovery (CRi)1Participants
Overall Response Rate (Phase II)Dose Level 3Partial Remission2Participants
Overall Response Rate (Phase II)Dose Level 3No remission/response17Participants
Overall Response Rate (Phase II)Dose Level 3Hematologic improvement without CR/PR0Participants
Toxicity Profile (Phase II)Dose Level 324Participants
Duration of ResponseDose Level 3252Full Range 14 to 517days
Overall Survival (Phase II)Dose Level 324495% Confidence Interval 203 to 467days

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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