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Trial · NCT03233724

Adverse events132

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherActivated partial thromboplastin time prolongedInvestigationsDecitabine 0.2mg/kg + Tetrahydrouridine 10mg/kg Sunday, Monday, Tuesday (SuMT)020
otherActivated partial thromboplastin time prolongedInvestigationsDecitabine 0.2mg/kg + Tetrahydrouridine 10mg/kg Monday-Tuesday (MT)020
otherActivated partial thromboplastin time prolongedInvestigationsDecitabine 0.2mg/kg + Tetrahydrouridine 10mg/kg Every (q) Tuesday,Wednesday (TW) x 2 Weeks q3Weeks141
otherActivated partial thromboplastin time prolongedInvestigationsDecitabine 0.17mg/kg + Tetrahydrouridine 10mg/kg Every (q) Tuesday,Wednesday (TW) x 2 Weeks q3Weeks000
otherAlkaline phosphatase increasedInvestigationsDecitabine 0.2mg/kg + Tetrahydrouridine 10mg/kg Sunday, Monday, Tuesday (SuMT)020
otherAlkaline phosphatase increasedInvestigationsDecitabine 0.2mg/kg + Tetrahydrouridine 10mg/kg Monday-Tuesday (MT)020
otherAlkaline phosphatase increasedInvestigationsDecitabine 0.2mg/kg + Tetrahydrouridine 10mg/kg Every (q) Tuesday,Wednesday (TW) x 2 Weeks q3Weeks244
otherAlkaline phosphatase increasedInvestigationsDecitabine 0.17mg/kg + Tetrahydrouridine 10mg/kg Every (q) Tuesday,Wednesday (TW) x 2 Weeks q3Weeks000
otherAnemiaBlood and lymphatic system disordersDecitabine 0.2mg/kg + Tetrahydrouridine 10mg/kg Sunday, Monday, Tuesday (SuMT)127
otherAnemiaBlood and lymphatic system disordersDecitabine 0.2mg/kg + Tetrahydrouridine 10mg/kg Monday-Tuesday (MT)121
otherAnemiaBlood and lymphatic system disordersDecitabine 0.2mg/kg + Tetrahydrouridine 10mg/kg Every (q) Tuesday,Wednesday (TW) x 2 Weeks q3Weeks040
otherAnemiaBlood and lymphatic system disordersDecitabine 0.17mg/kg + Tetrahydrouridine 10mg/kg Every (q) Tuesday,Wednesday (TW) x 2 Weeks q3Weeks000
otherBlood bilirubin increasedInvestigationsDecitabine 0.2mg/kg + Tetrahydrouridine 10mg/kg Sunday, Monday, Tuesday (SuMT)121
otherBlood bilirubin increasedInvestigationsDecitabine 0.2mg/kg + Tetrahydrouridine 10mg/kg Monday-Tuesday (MT)122
otherBlood bilirubin increasedInvestigationsDecitabine 0.2mg/kg + Tetrahydrouridine 10mg/kg Every (q) Tuesday,Wednesday (TW) x 2 Weeks q3Weeks040
otherBlood bilirubin increasedInvestigationsDecitabine 0.17mg/kg + Tetrahydrouridine 10mg/kg Every (q) Tuesday,Wednesday (TW) x 2 Weeks q3Weeks000
otherBlurred visionEye disordersDecitabine 0.2mg/kg + Tetrahydrouridine 10mg/kg Sunday, Monday, Tuesday (SuMT)121
otherBlurred visionEye disordersDecitabine 0.2mg/kg + Tetrahydrouridine 10mg/kg Monday-Tuesday (MT)020
otherBlurred visionEye disordersDecitabine 0.2mg/kg + Tetrahydrouridine 10mg/kg Every (q) Tuesday,Wednesday (TW) x 2 Weeks q3Weeks040
otherBlurred visionEye disordersDecitabine 0.17mg/kg + Tetrahydrouridine 10mg/kg Every (q) Tuesday,Wednesday (TW) x 2 Weeks q3Weeks000

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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