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Trial · NCT02819804

Outcomes15

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYIncidence of Dose-Limiting Toxicity (DLT)Up to 28 days
Only one patient was treated on study and this patient did not complete the DLT period and was not evaluable for this outcome measure or any of the outcome measures. Sample size too small for analysis.
SECONDARYIncidence of Adverse EventsUp to 28-days after the last dose
SECONDARYRate of Complete Hematologic Remission (CR)At 84 days (3 cycles)
SECONDARYRate of Molecular RemissionAt 84 days (3 cycles)
SECONDARYSerum Level of Dasatinib24 hours after the start of cycle 1 and days 8, 15, and 22 prior to treatment during cycle 1
SECONDARYSerum Level of NivolumabDays 8, 15, and 22 prior to treatment during cycle 1
SECONDARYPD1 Expression Levels and Saturation Assessed in the Peripheral BloodBaseline to 28-days after the last dose
SECONDARYPD1 Expression Levels and Saturation in Bone MarrowBaseline to 28-days after the last dose
SECONDARYPeripheral T-cell Levels and Activation in Response to TreatmentAt cycle 1 days: 1, 2, 8, 15, & 22 prior to dosing
OTHER_PRE_SPECIFIEDThe 30 Day Mortality RateUp to 30 days
OTHER_PRE_SPECIFIEDOverall Survival (OS)Up to 1 year
OTHER_PRE_SPECIFIEDProgression Free Survival (PFS)Up to 1 year
OTHER_PRE_SPECIFIEDDuration of Remission (DOR)Up to 1 year
OTHER_PRE_SPECIFIEDCompare the OS Between Patients Who Receive a Hematopoietic Stem Cell Transplant and Those Who Receive no Further Therapy Following RemissionUp to 1 year
OTHER_PRE_SPECIFIEDPresence of Resistance Mutations in Bone Marrow at the Time of Disease ProgressionUp to 28-days after the last dose

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.

For software

Read this list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT02819804/outcomes