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Trial · NCT05568225

Results by group99

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

OutcomeGroupCategoryValueSpreadUnits
Percentage of Participants With Hematologic Improvement- Erythroid (HI-E) Response for >=8 Weeks Within 24 Weeks of Etavopivat TreatmentNon-transfusion Dependent0Percentage of participants
Percentage of Participants With Hematologic Improvement- Erythroid (HI-E) Response for >=8 Weeks Within 24 Weeks of Etavopivat TreatmentLow Transfusion Burden50Percentage of participants
Percentage of Participants With Hematologic Improvement- Erythroid (HI-E) Response for >=8 Weeks Within 24 Weeks of Etavopivat TreatmentHigh Transfusion Burden25Percentage of participants
Number of All Adverse Events (AEs), Serious Adverse Events (SAEs), and AEs Related to EtavopivatNon-transfusion DependentAE33Events
Number of All Adverse Events (AEs), Serious Adverse Events (SAEs), and AEs Related to EtavopivatLow Transfusion BurdenAE33Events
Number of All Adverse Events (AEs), Serious Adverse Events (SAEs), and AEs Related to EtavopivatHigh Transfusion BurdenAE54Events
Number of All Adverse Events (AEs), Serious Adverse Events (SAEs), and AEs Related to EtavopivatNon-transfusion DependentSAE1Events
Number of All Adverse Events (AEs), Serious Adverse Events (SAEs), and AEs Related to EtavopivatLow Transfusion BurdenSAE0Events
Number of All Adverse Events (AEs), Serious Adverse Events (SAEs), and AEs Related to EtavopivatHigh Transfusion BurdenSAE6Events
Number of All Adverse Events (AEs), Serious Adverse Events (SAEs), and AEs Related to EtavopivatNon-transfusion DependentAEs related to etavopivat0Events
Number of All Adverse Events (AEs), Serious Adverse Events (SAEs), and AEs Related to EtavopivatLow Transfusion BurdenAEs related to etavopivat0Events
Number of All Adverse Events (AEs), Serious Adverse Events (SAEs), and AEs Related to EtavopivatHigh Transfusion BurdenAEs related to etavopivat1Events
Number of All Adverse Events (AEs), Serious Adverse Events (SAEs), and AEs Related to EtavopivatNon-transfusion DependentAEs possibly related etavopivat8Events
Number of All Adverse Events (AEs), Serious Adverse Events (SAEs), and AEs Related to EtavopivatLow Transfusion BurdenAEs possibly related etavopivat3Events
Number of All Adverse Events (AEs), Serious Adverse Events (SAEs), and AEs Related to EtavopivatHigh Transfusion BurdenAEs possibly related etavopivat6Events
Number of Premature Discontinuations, Dose Interruptions, and Dose ReductionsNon-transfusion DependentPremature discontinuations1Events
Number of Premature Discontinuations, Dose Interruptions, and Dose ReductionsLow Transfusion BurdenPremature discontinuations0Events
Number of Premature Discontinuations, Dose Interruptions, and Dose ReductionsHigh Transfusion BurdenPremature discontinuations0Events
Number of Premature Discontinuations, Dose Interruptions, and Dose ReductionsNon-transfusion DependentDose interruptions0Events
Number of Premature Discontinuations, Dose Interruptions, and Dose ReductionsLow Transfusion BurdenDose interruptions0Events

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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