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Comparison · NCT01773187-bf6606eb

Pacritinib vs Best Available Therapy: Spleen Volume Reduction

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Pacritinib vs Best Available Therapy: Spleen Volume Reduction. Trial comparisons, record NCT01773187-bf6606eb. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01773187-bf6606eb

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.1910.1440.248wilson
Risk in group 20.04670.02010.105wilson
Risk difference, group 1 minus group 20.1440.06990.207newcombe hybrid score
Risk ratio, group 1 over group 24.091.6610log
Odds ratio, group 1 over group 24.811.8512.6log
Number needed to treat, for one more participant with the outcome on Pacritinib than on Best Available Therapy6.944.8314.3from the risk difference interval

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1PacritinibPacritinib 400 mg QD42220OG000
Group 2Best Available TherapyBAT includes any physician-selected treatment for primary or secondary myelofibrosis with the exclusion of JAK inhibitors (inhibitors of Janus kinases).5107OG001

Outcome

Type
PRIMARY
Title
Spleen Volume Reduction
Description
Number of patients achieving a ≥ 35% reduction in spleen volume from baseline to week 24 as measured by magnetic resonance imaging (MRI) or computed tomography (CT)
Time frame
Baseline to Week 24
Population

Source ClinicalTrials.gov

Trial

Title
Pacritinib Versus Best Available Therapy to Treat Myelofibrosis
NCT number
NCT01773187
Phases
PHASE3
Conditions
Primary Myelofibrosis, Post-polycythemia Vera Myelofibrosis, Post-essential Thrombocythemia Myelofibrosis
Interventions
Pacritinib, Best Available Therapy
Lead sponsor
CTI BioPharma
Results first posted
2020-09-29

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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