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Trial · NCT07012044

Registered outcomes11

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryMaximum tolerated dose of ASTX727Up to completion of cycle 2 (cycle length=28 days)Defined as maximum dose at which fewer than one-third of patients experience dose limiting toxicity.
PrimaryIncidence of adverse events of ASTX727Up to 2 yearsWill be graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events version 5.0.
PrimaryArea under the concentration by time curve of ASTX727Up to 28 daysMedian area under the concentration over time curve assessed at 1 and 3 hours post dose in cycle 1 stratified by dose level.
PrimaryHalf life of ASTX727Up to 28 daysMedian half-life of ASTX727 stratified by dose level assessed at 1 and 3 hours post dose in cycle 1 stratified by dose level.
PrimaryClearance of ASTX727Up to 28 daysMedian clearance of ASTX727 assessed at 1 and 3 hours post dose in cycle 1 stratified by dose level.
SecondaryIncidence of graft versus host disease of ASTX727Up to 2 yearsFrequency of graft versus host disease stratified by dose level.
SecondarySeverity of graft versus host disease of ASTX727Up to 2 yearsFrequency of graft versus host disease severity score stratified by dose level.
SecondaryIncidence of graft rejection of ASTX727Up to 2 yearsFrequency of graft rejection stratified by dose level.
SecondarySeverity of graft rejection of ASTX727Up to 2 yearsFrequency of graft rejection severity score by dose level.
SecondaryEvent free survival of ASTX727At 1 yearMedian time to event stratified by dose level.
OtherPharmacodynamic profile of ASTX727At cycle 1 day 1 and cycle 1 day 8Assessed through deoxyribonucleic acid methylation assay.

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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