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NCT02055781 · ClinicalTrials.gov registry record · Phase 3

Pacritinib Versus Best Available Therapy to Treat Patients With Myelofibrosis and Thrombocytopenia

A Phase 3 study, sponsored by CTI BioPharma.

Terminated
Registry status
Phase 3
Development phase
311
Enrollment target

NCT02055781: Clinical Trial Phase 3 study, sponsored by CTI BioPharma.

NCT02055781 is a Phase 3 study that was terminated before completion, run by CTI BioPharma. The registered enrollment target is 311 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (60% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT02055781, a Phase 3 study, was terminated before completion, sponsored by CTI BioPharma.

TERMINATED
Registry status
Phase 3
Development phase
311 participants
Enrollment target

Study Summary

Phase 3, randomized, controlled study to evaluate the safety and efficacy of oral pacritinib compared to Best Available Therapy (BAT) in patients with thrombocytopenia and primary or secondary myelofibrosis.

Primary Outcome

Proportion 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).

Interventions

  • DRUG Pacritinib
  • DRUG Best Available Therapy

Trial Details

FieldValue
Enrollment Target 311 participants
Start Date 2014-02
Est. Completion 2016-04
Phase Phase 3
CTI BioPharma

28 total trials

Why NCT02055781 stopped before completion

NCT02055781 is an interventional study that assigns participants to a tested intervention. The registered 311 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (60% lower).

The record links to 0 conditions, and to 2 interventions - of which Pacritinib is the first listed.

NCT02055781 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02055781 about?

NCT02055781 is a clinical study titled "Pacritinib Versus Best Available Therapy to Treat Patients With Myelofibrosis and Thrombocytopenia". Phase 3, randomized, controlled study to evaluate the safety and efficacy of oral pacritinib compared to Best Available Therapy (BAT) in patients with thrombocytopenia and primary or secondary myelofibrosis.

What is the current status of trial NCT02055781?

This trial is currently terminated. It is a Phase 3 study. The enrollment target is 311 participants. The study started on 2014-02. Estimated completion is 2016-04.

What interventions are being tested in trial NCT02055781?

The interventions under investigation include: Pacritinib (DRUG), Best Available Therapy (DRUG).

Who is sponsoring clinical trial NCT02055781?

This trial is sponsored by CTI BioPharma, which has 28 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02055781's enrollment target sits among peer trials

311 1106th of 2000 higher than 894 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02055781, the US trial registry maintained by the National Library of Medicine. NCT02055781 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.