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Trial · NCT02515630

Outcomes25

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYTransfusion Independence Response by Week 24From baseline to Week 24
Assessed in the Safety Analysis Set, which includes all subjects who received ≥ 1 dose of momelotinib. Note that 6 subjects discontinued prior to Week 12 and could not be evaluated over the minimum period required for assessment of the endpoint (12 weeks).
percentage of subjectsNUMBER
SECONDARYTransfusion Response Rate by Week 24From baseline to Week 24
Assessed in the Safety Analysis Set, which includes all subjects who received ≥ 1 dose of momelotinib. Note that 3 subjects discontinued prior to Week 8 and could not be evaluated over the minimum period required for assessment of the endpoint (8 weeks).
percentage of subjectsNUMBER
SECONDARYSplenic Response Rate at Week 24Measured at Week 24Assessed in the Safety Analysis Set, which includes all subjects who received ≥ 1 dose of momelotinib. Note that spleen volume at Week 24 was not available for 15 subjects.percentage of subjectsNUMBER
SECONDARYResponse Rate in Total Symptom Score (TSS) at Week 24Measured at Week 24There were 3 subjects with missing TSS at baseline who were excluded from the analysis. Note that of the 38 subjects evaluated, 17 were missing Week 24 TSS assessments.percentage of subjectsNUMBER
SECONDARYChange in Markers of Iron Metabolism and Anemia - Change From Baseline in Hepcidin Daily ChangeAt baseline, Day 1, Weeks 2, 4, 8, 12, 16, 20 and 24nMMEDIAN
SECONDARYChange in Markers of Iron Metabolism and Anemia - Trough HepcidinAt baseline, Day 1, Weeks 2, 4, 8, 12, 16, 20 and 24nMMEDIAN
SECONDARYChange in Markers of Iron Metabolism and Anemia - Serum IronAt Weeks 2, 4, 8, 12, 16, 20 and 24% Change from baselineMEDIAN
SECONDARYChange in Markers of Iron Metabolism and Anemia - HemoglobinAt Weeks 2, 4, 8, 12, 16, 20 and 24% Change in from baselineMEDIAN
SECONDARYChange in Markers of Iron Metabolism and Anemia - Total Iron Binding CapacityAt Weeks 2, 4, 8, 12, 16, 20 and 24% Change from baselineMEDIAN
SECONDARYChange in Markers of Iron Metabolism and Anemia - ReticulocytesAt Weeks 2, 4, 8, 12, 16, 20 and 24% Change from baselineMEDIAN
SECONDARYChange in Markers of Iron Metabolism and Anemia - Reticulocytes/Erythrocytes%At Weeks 2, 4, 8, 12, 16, 20 and 24% Change from baselineMEDIAN
SECONDARYChange in Markers of Iron Metabolism and Anemia - ErythropoietinAt Weeks 8 and 20% Change from baselineMEDIAN
SECONDARYChange in Markers of Iron Metabolism and Anemia - ErythrocytesAt Weeks 2, 4, 8, 12, 16, 20 and 24% Change from baselineMEDIAN
SECONDARYChange in Markers of Iron Metabolism and Anemia - HematocritAt Weeks 2, 4, 8, 12, 16, 20 and 24% Change from baselineMEDIAN
SECONDARYChange in Markers of Iron Metabolism and Anemia - FerritinAt Weeks 2, 4, 8, 12, 16, 20 and 24% Change from baselineMEDIAN
SECONDARYChange in Markers of Iron Metabolism and Anemia - Soluble Transferrin ReceptorAt Weeks 2, 4, 8, 12, 16, 20 and 24% Change from baselineMEDIAN
SECONDARYChange in Markers of Iron Metabolism and Anemia - Transferrin SaturationAt Weeks 2, 4, 8, 12, 16, 20 and 24% Change from baselineMEDIAN
SECONDARYChange in Markers of Iron Metabolism and Anemia - Unsaturated Iron Binding CapacityAt Weeks 2, 4, 8, 12, 16, 20 and 24% Change from baselineMEDIAN
SECONDARYChange in Markers of Iron Metabolism and Anemia - PlateletsAt Weeks 2, 4, 8, 12, 16, 20 and 24% Change from baselineMEDIAN
SECONDARYChange in Markers of Iron Metabolism and Anemia - LeukocytesAt Weeks 2, 4, 8, 12, 16, 20 and 24% Change from baselineMEDIAN

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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