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NCT02493530 · ClinicalTrials.gov registry record · Phase 1

TGR-1202 + Ruxolitinib PMF PPV-MF PET-MF MDS/MPN Polycythemia Vera Resistant to Hydroxyurea

A Phase 1 study of Myelofibrosis and Polycythemia Vera, sponsored by Vanderbilt-Ingram Cancer Center.

Completed
Registry status
Phase 1
Development phase
60
Enrollment target
5
Study locations

NCT02493530 is a Phase 1 study of Myelofibrosis and Polycythemia Vera that has completed, run by Vanderbilt-Ingram Cancer Center. The registered enrollment target is 60 participants, below the 195-participant average among 61 other Myelofibrosis trials with a reported enrollment target (69% lower). The trial reports 5 study locations across 5 states.

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The verdict

NCT02493530, a Phase 1 study of Myelofibrosis and Polycythemia Vera, has completed, sponsored by Vanderbilt-Ingram Cancer Center.

COMPLETED
Registry status
Phase 1
Development phase
60 participants
Enrollment target
5
Study locations

Study Summary

This is a Phase 1, open-label, study of TGR-1202, a PI3K delta inhibitor, administered together with ruxolitinib in patients with myeloproliferative neoplasms (specifically: polycythemia vera, primary myelofibrosis, PPV-MF or PET-MF) and MDS/MPN.

Interventions

  • DRUG ruxolitinib
  • DRUG TGR-1202

Study Locations (5)

Arizona

  • Mayo Clinic - Arizona - Phoenix

Colorado

  • University of Colorado Cancer Center - Aurora

Tennessee

  • Vanderbilt-Ingram Cancer Center - Nashville

Texas

  • Mays Cancer Center at University of Texas Health San Antonio - San Antonio

Wisconsin

  • Medical College of Wisconsin - Milwaukee

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2015-07
Est. Completion 2024-05
Phase Phase 1

Sponsor

Vanderbilt-Ingram Cancer Center

189 total trials

What the Registry Record Tells You About NCT02493530

The ClinicalTrials.gov registry entry for NCT02493530 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 195-participant average among 61 other Myelofibrosis trials with a reported enrollment target (69% lower). The listed sponsor is Vanderbilt-Ingram Cancer Center, which has 189 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Myelofibrosis appearing as the primary indexed condition, and to 2 interventions - of which ruxolitinib is the first listed.

NCT02493530 reports 5 study locations spanning 5 distinct geographic areas - top geographies include Arizona, Colorado, Tennessee.

Frequently Asked Questions

What is clinical trial NCT02493530 about?

NCT02493530 is a clinical study titled "TGR-1202 + Ruxolitinib PMF PPV-MF PET-MF MDS/MPN Polycythemia Vera Resistant to Hydroxyurea". This is a Phase 1, open-label, study of TGR-1202, a PI3K delta inhibitor, administered together with ruxolitinib in patients with myeloproliferative neoplasms (specifically: polycythemia vera, primary myelofibrosis, PPV-MF or PET-MF) and MDS/MPN.

What is the current status of trial NCT02493530?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 60 participants. The study started on 2015-07. Estimated completion is 2024-05.

What conditions does trial NCT02493530 study?

This clinical trial studies the following conditions: Myelofibrosis, Polycythemia Vera.

What interventions are being tested in trial NCT02493530?

The interventions under investigation include: ruxolitinib (DRUG), TGR-1202 (DRUG).

Who is sponsoring clinical trial NCT02493530?

This trial is sponsored by Vanderbilt-Ingram Cancer Center, which has 189 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02493530 being conducted?

This trial has 5 study locations across Arizona, Colorado, Tennessee, Texas, Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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