Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02267278 · ClinicalTrials.gov registry record · Phase 2

Ruxolitinib and Pracinostat Combination Therapy for Patients With Myelofibrosis (MF)

A Phase 2 study, sponsored by M.D. Anderson Cancer Center.

Completed
Registry status
Phase 2
Development phase
25
Enrollment target

NCT02267278: Completed Phase 2 study, sponsored by M.D. Anderson Cancer Center.

NCT02267278 is a Phase 2 study that has completed, run by M.D. Anderson Cancer Center. The registered enrollment target is 25 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (81% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT02267278, a Phase 2 study, has completed, sponsored by M.D. Anderson Cancer Center.

COMPLETED
Registry status
Phase 2
Development phase
25 participants
Enrollment target

Study Summary

The goal of this clinical research study is to learn if pracinostat, when given in combination with ruxolitinib, can help to control myelofibrosis (MF). The safety of this drug combination will also be studied. This is an investigational study. Pracinostat is not FDA-approved or commercially available. It is currently being used for research purposes only. Ruxolitinib is FDA-approved and commercially available to treat MF. The study doctor can explain how the study drugs are designed to work. Up to 25 participants will be enrolled in this study. All will take part at MD Anderson.

Primary Outcome

Objective response rate (ORR), defined as a clinical improvement (CI), partial remission (PR), and complete remission (CR) according to the International Working Group (IWG) Criteria. Complete remission (CR): bone marrow blasts \<5%, hemoglobin \>/= 10, absolute neutrophil count (ANC) \>/= 1000, platelets \>/= 100, \<2% immature myeloid cell, spleen and liver not palpable. Partial Response (PR): CR plus one or more of the following: ANC \>/= 1000, decreased platelets by 50%, hemoglobin \>/= 8.5

Interventions

  • DRUG Ruxolitinib
  • BEHAVIORAL Questionnaire
  • DRUG Pracinostat

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2015-01-12
Est. Completion 2018-06-01
Phase Phase 2
M.D. Anderson Cancer Center

2,692 total trials

What the finished NCT02267278 record still lists

NCT02267278 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 25 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (81% lower).

The record links to 0 conditions, and to 3 interventions - of which Ruxolitinib is the first listed.

NCT02267278 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02267278 about?

NCT02267278 is a clinical study titled "Ruxolitinib and Pracinostat Combination Therapy for Patients With Myelofibrosis (MF)". The goal of this clinical research study is to learn if pracinostat, when given in combination with ruxolitinib, can help to control myelofibrosis (MF). The safety of this drug combination will also be studied. This is an investigational study. Pracinostat is not FDA-approved or commercially availa...

What is the current status of trial NCT02267278?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 25 participants. The study started on 2015-01-12. Estimated completion is 2018-06-01.

What interventions are being tested in trial NCT02267278?

The interventions under investigation include: Ruxolitinib (DRUG), Questionnaire (BEHAVIORAL), Pracinostat (DRUG).

Who is sponsoring clinical trial NCT02267278?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02267278's enrollment target sits among peer trials

25 1719th of 2000 higher than 245 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01166854 · 25 participants

    Characterization of Familial Myopathy and Paget Disease of Bone

  • NCT01913106 · 25 participants · Phase 1

    HSV-tk + Valacyclovir Therapy in Combination With Brachytherapy for Recurrent Prostate Cancer

  • NCT02138669 · 25 participants · NA

    Intacs Prescription Inserts for Keratoconus Patients

  • NCT02174549 · 25 participants · Phase 1

    Dose-defining Study of Tirapazamine Combined With Embolization in Liver Cancer

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT02267278, the US trial registry maintained by the National Library of Medicine. NCT02267278 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.