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Comparison · NCT01773187-deaths

Pacritinib vs Best Available Therapy: deaths from any cause

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: deaths from any cause. Trial comparisons, record NCT01773187-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01773187-deaths

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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 10.1230.08570.173wilson
Risk in group 20.02830.009670.0799wilson
Risk difference, group 1 minus group 20.09440.03090.148newcombe hybrid score
Risk ratio, group 1 over group 24.341.3514log
Odds ratio, group 1 over group 24.81.4216.2log
Number needed to harm, for one more death from any cause on Pacritinib than on Best Available Therapy10.66.7732.3from 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 QD27220EG000
Group 2Best Available TherapyBAT includes any physician-selected treatment for primary or secondary myelofibrosis with the exclusion of JAK inhibitors (inhibitors of Janus kinases).3106EG001

Harm

What it counts
Total, all-cause mortality
Time frame
Time of signing informed consent through 30 days after the last study treatment.

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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