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NCT03222609 · ClinicalTrials.gov registry record · Phase 2

A Study Evaluating Tolerability and Efficacy of Navitoclax Alone or in Combination With Ruxolitinib in Participants With Myelofibrosis

A Phase 2 study of Myelofibrosis (MF), sponsored by AbbVie.

Completed
Registry status
Phase 2
Development phase
191
Enrollment target
20
Study locations

NCT03222609: Completed Phase 2 study of Myelofibrosis (MF), sponsored by AbbVie.

NCT03222609 is a Phase 2 study of Myelofibrosis (MF) that has completed, run by AbbVie. The registered enrollment target is 191 participants, below the 954-participant average among 6 other Myelofibrosis (MF) trials with a reported enrollment target (80% lower). The trial reports 20 study locations across 11 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03222609, a Phase 2 study of Myelofibrosis (MF), has completed, sponsored by AbbVie.

COMPLETED
Registry status
Phase 2
Development phase
191 participants
Enrollment target
20
Study locations

Study Summary

This is a Phase 2 open-label, multicenter study evaluating tolerability and efficacy of navitoclax alone or when added to ruxolitinib in participants with myelofibrosis.

Primary Outcome

Reduction in spleen volume is measured by magnetic resonance imaging/computerized tomography (MRI/CT).

Conditions Studied

Interventions

  • DRUG Ruxolitinib
  • DRUG Navitoclax

Study Locations (20)

California

  • TOI Clinical Research /ID# 222546 - Cerritos
  • City of Hope /ID# 221395 - Duarte
  • Moores Cancer Center at UC San Diego /ID# 164084 - La Jolla
  • Long Beach Memorial Medical Ct /ID# 230148 - Long Beach
  • University of Southern California /ID# 164095 - Los Angeles

Florida

  • Baptist MD Anderson Cancer Center - Jacksonville /ID# 222548 - Jacksonville
  • Mayo Clinic /ID# 164201 - Jacksonville
  • Moffitt Cancer Center /ID# 164082 - Tampa

Illinois

  • University of Chicago Medicine /ID# 164115 - Chicago
  • Mid Illinois Hematology & Oncology Associates, Ltd /ID# 230536 - Normal

Massachusetts

  • Dana-Farber Cancer Institute /ID# 162675 - Boston
  • University of Massachusetts - Worcester /ID# 222547 - Worcester

Michigan

  • Henry Ford Hospital /ID# 162682 - Detroit
  • Ascension Providence Southfield Cancer Center /ID# 223876 - Southfield

Alabama

  • UAB Comprehensive Cancer Cente /ID# 165464 - Birmingham

Colorado

  • Colorado Blood Cancer Institute /ID# 224250 - Denver

Indiana

  • Indiana Blood & Marrow Transpl /ID# 165075 - Indianapolis

Trial Details

FieldValue
Enrollment Target 191 participants
Start Date 2017-10-31
Est. Completion 2025-01-29
Phase Phase 2
AbbVie

526 total trials

What the finished NCT03222609 record still lists

NCT03222609 is an interventional study that assigns participants to a tested intervention. The registered 191 participants enrollment target is mid-sized for trials with a published cap, below the 954-participant average among 6 other Myelofibrosis (MF) trials with a reported enrollment target (80% lower).

The record links to 1 condition, with Myelofibrosis (MF) appearing as the primary indexed condition, and to 2 interventions - of which Ruxolitinib is the first listed.

NCT03222609 names 20 study sites across 11 states, led by California, Florida, Illinois.

Frequently Asked Questions

What is clinical trial NCT03222609 about?

NCT03222609 is a clinical study titled "A Study Evaluating Tolerability and Efficacy of Navitoclax Alone or in Combination With Ruxolitinib in Participants With Myelofibrosis". This is a Phase 2 open-label, multicenter study evaluating tolerability and efficacy of navitoclax alone or when added to ruxolitinib in participants with myelofibrosis.

What is the current status of trial NCT03222609?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 191 participants. The study started on 2017-10-31. Estimated completion is 2025-01-29.

What conditions does trial NCT03222609 study?

This clinical trial studies the following conditions: Myelofibrosis (MF).

What interventions are being tested in trial NCT03222609?

The interventions under investigation include: Ruxolitinib (DRUG), Navitoclax (DRUG).

Who is sponsoring clinical trial NCT03222609?

This trial is sponsored by AbbVie, which has 526 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03222609 being conducted?

This trial has 20 study locations across Alabama, California, Colorado, Florida, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Myelofibrosis (MF)

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Nationwide trials with similar profiles

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

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Source: ClinicalTrials.gov NCT03222609, the US trial registry maintained by the National Library of Medicine. NCT03222609 (mid enrollment · wide site footprint · completed) retrieved and formatted by PlainTrial, see methodology.