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Trial · NCT01202877

Results by group15

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

OutcomeGroupCategoryValueSpreadUnits
Participant Best Response Assessed Using Response Evaluation Criteria In Solid Tumors (RECIST) Version 1.1Phase I: 5-azacytidine + PKC412 25 mgComplete Remission (CR)0participants
Participant Best Response Assessed Using Response Evaluation Criteria In Solid Tumors (RECIST) Version 1.1Phase I: 5-azacytidine + PKC412 50 mgComplete Remission (CR)0participants
Participant Best Response Assessed Using Response Evaluation Criteria In Solid Tumors (RECIST) Version 1.1Phase II: 5-azacytidine + PKC412Complete Remission (CR)1participants
Participant Best Response Assessed Using Response Evaluation Criteria In Solid Tumors (RECIST) Version 1.1Phase I: 5-azacytidine + PKC412 25 mgComplete w/Incomplete Bone Marrow Recovery (CRi)1participants
Participant Best Response Assessed Using Response Evaluation Criteria In Solid Tumors (RECIST) Version 1.1Phase I: 5-azacytidine + PKC412 50 mgComplete w/Incomplete Bone Marrow Recovery (CRi)1participants
Participant Best Response Assessed Using Response Evaluation Criteria In Solid Tumors (RECIST) Version 1.1Phase II: 5-azacytidine + PKC412Complete w/Incomplete Bone Marrow Recovery (CRi)4participants
Participant Best Response Assessed Using Response Evaluation Criteria In Solid Tumors (RECIST) Version 1.1Phase I: 5-azacytidine + PKC412 25 mgMorphologic Leukemia-Free Status (MLFS)0participants
Participant Best Response Assessed Using Response Evaluation Criteria In Solid Tumors (RECIST) Version 1.1Phase I: 5-azacytidine + PKC412 50 mgMorphologic Leukemia-Free Status (MLFS)0participants
Participant Best Response Assessed Using Response Evaluation Criteria In Solid Tumors (RECIST) Version 1.1Phase II: 5-azacytidine + PKC412Morphologic Leukemia-Free Status (MLFS)6participants
Participant Best Response Assessed Using Response Evaluation Criteria In Solid Tumors (RECIST) Version 1.1Phase I: 5-azacytidine + PKC412 25 mgPartial Remission (PR)0participants
Participant Best Response Assessed Using Response Evaluation Criteria In Solid Tumors (RECIST) Version 1.1Phase I: 5-azacytidine + PKC412 50 mgPartial Remission (PR)0participants
Participant Best Response Assessed Using Response Evaluation Criteria In Solid Tumors (RECIST) Version 1.1Phase II: 5-azacytidine + PKC412Partial Remission (PR)1participants
Overall Response (OR) Within 6 MonthsPhase I: 5-azacytidine + PKC412 25 mg1participants
Overall Response (OR) Within 6 MonthsPhase I: 5-azacytidine + PKC412 50 mg1participants
Overall Response (OR) Within 6 MonthsPhase II: 5-azacytidine + PKC41212participants

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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