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NCT03572764 · ClinicalTrials.gov registry record · Phase 1

CPX-351 (Vyxeos™) for Transplant Eligible, Higher Risk Patients With Myelodysplastic Syndrome

A Phase 1 study of Myelodysplastic Syndromes, sponsored by Washington University School of Medicine.

Active
Registry status
Phase 1
Development phase
20
Enrollment target
3
Study locations

NCT03572764 is a Phase 1 study of Myelodysplastic Syndromes that is active but no longer recruiting, run by Washington University School of Medicine. The registered enrollment target is 20 participants, below the 285-participant average among 173 other Myelodysplastic Syndromes trials with a reported enrollment target (93% lower). The trial reports 3 study locations across 3 states.

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The verdict

NCT03572764, a Phase 1 study of Myelodysplastic Syndromes, is active but no longer recruiting, sponsored by Washington University School of Medicine.

ACTIVE NOT RECRUITING
Registry status
Phase 1
Development phase
20 participants
Enrollment target
3
Study locations

Study Summary

This is a pilot and feasibility study of transplant eligible, higher risk myelodysplastic syndrome (MDS) patients to determine the safety and tolerability of a lower -dose and higher-dose CPX-351 regimen, with secondary objectives including complete remission (CR) rates and proportion of patients proceeding to transplant.

Conditions Studied

Interventions

  • DRUG CPX-351
  • PROCEDURE Research blood draw
  • PROCEDURE Research skin biopsy
  • PROCEDURE Research bone marrow aspirate

Study Locations (3)

Florida

  • Moffitt Cancer Center - Tampa

Missouri

  • Washington University School of Medicine - St Louis

Washington

  • Fred Hutchinson Cancer Research Center - Seattle

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2018-12-14
Est. Completion 2027-03-25
Phase Phase 1

What the Registry Record Tells You About NCT03572764

The ClinicalTrials.gov registry entry for NCT03572764 describes a study currently listed as active not recruiting, categorized as Phase 1. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 285-participant average among 173 other Myelodysplastic Syndromes trials with a reported enrollment target (93% lower). The listed sponsor is Washington University School of Medicine, which has 1,502 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Myelodysplastic Syndromes appearing as the primary indexed condition, and to 4 interventions - of which CPX-351 is the first listed.

NCT03572764 reports 3 study locations spanning 3 distinct geographic areas - top geographies include Florida, Missouri, Washington.

Frequently Asked Questions

What is clinical trial NCT03572764 about?

NCT03572764 is a clinical study titled "CPX-351 (Vyxeos™) for Transplant Eligible, Higher Risk Patients With Myelodysplastic Syndrome". This is a pilot and feasibility study of transplant eligible, higher risk myelodysplastic syndrome (MDS) patients to determine the safety and tolerability of a lower -dose and higher-dose CPX-351 regimen, with secondary objectives including complete remission (CR) rates and proportion of patients pr...

What is the current status of trial NCT03572764?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2018-12-14. Estimated completion is 2027-03-25.

What conditions does trial NCT03572764 study?

This clinical trial studies the following conditions: Myelodysplastic Syndromes.

What interventions are being tested in trial NCT03572764?

The interventions under investigation include: CPX-351 (DRUG), Research blood draw (PROCEDURE), Research skin biopsy (PROCEDURE), Research bone marrow aspirate (PROCEDURE).

Who is sponsoring clinical trial NCT03572764?

This trial is sponsored by Washington University School of Medicine, which has 1,502 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03572764 being conducted?

This trial has 3 study locations across Florida, Missouri, Washington. 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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