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NCT04055844 · ClinicalTrials.gov registry record · Phase 2

Multi-Ctr PII Cmb.Modality Tx Ruxolitinib, Decitabine, and DLI for Post HSCT in AML/MDS

A Phase 2 study of Acute Myeloid Leukemia and Myelodysplastic Syndromes, sponsored by Masonic Cancer Center, University of Minnesota.

Completed
Registry status
Phase 2
Development phase
14
Enrollment target
3
Study locations

NCT04055844 is a Phase 2 study of Acute Myeloid Leukemia and Myelodysplastic Syndromes that has completed, run by Masonic Cancer Center, University of Minnesota. The registered enrollment target is 14 participants, below the 116-participant average among 306 other Acute Myeloid Leukemia trials with a reported enrollment target (88% lower). The trial reports 3 study locations across 3 states.

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The verdict

NCT04055844, a Phase 2 study of Acute Myeloid Leukemia and Myelodysplastic Syndromes, has completed, sponsored by Masonic Cancer Center, University of Minnesota.

COMPLETED
Registry status
Phase 2
Development phase
14 participants
Enrollment target
3
Study locations

Study Summary

This is a multi-center, single-arm, open-label, phase II trial for the frontline treatment of relapsed AML or MDS following allo-HCT. Eligible subjects will receive up to 4 cycles of combined modality treatment. The number of cycles depends on response, toxicity, and the remaining cell dose.

Interventions

  • DRUG Decitabine
  • DRUG Ruxolitinib
  • DRUG Donor Lymphocyte Infusion (DLI)

Study Locations (3)

Minnesota

  • Masonic Cancer Center, University of Minnesota - Minneapolis

Missouri

  • Washington University Medical School - St Louis

New York

  • University of Rochester Medical Center - Rochester

Trial Details

FieldValue
Enrollment Target 14 participants
Start Date 2020-02-17
Est. Completion 2022-09-06
Phase Phase 2

What the Registry Record Tells You About NCT04055844

The ClinicalTrials.gov registry entry for NCT04055844 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 14 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 116-participant average among 306 other Acute Myeloid Leukemia trials with a reported enrollment target (88% lower). The listed sponsor is Masonic Cancer Center, University of Minnesota, which has 249 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Acute Myeloid Leukemia appearing as the primary indexed condition, and to 3 interventions - of which Decitabine is the first listed.

NCT04055844 reports 3 study locations spanning 3 distinct geographic areas - top geographies include Minnesota, Missouri, New York.

Frequently Asked Questions

What is clinical trial NCT04055844 about?

NCT04055844 is a clinical study titled "Multi-Ctr PII Cmb.Modality Tx Ruxolitinib, Decitabine, and DLI for Post HSCT in AML/MDS". This is a multi-center, single-arm, open-label, phase II trial for the frontline treatment of relapsed AML or MDS following allo-HCT. Eligible subjects will receive up to 4 cycles of combined modality treatment. The number of cycles depends on response, toxicity, and the remaining cell dose.

What is the current status of trial NCT04055844?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 14 participants. The study started on 2020-02-17. Estimated completion is 2022-09-06.

What conditions does trial NCT04055844 study?

This clinical trial studies the following conditions: Acute Myeloid Leukemia, Myelodysplastic Syndromes, Myeloid and Monocytic Leukemia.

What interventions are being tested in trial NCT04055844?

The interventions under investigation include: Decitabine (DRUG), Ruxolitinib (DRUG), Donor Lymphocyte Infusion (DLI) (DRUG).

Who is sponsoring clinical trial NCT04055844?

This trial is sponsored by Masonic Cancer Center, University of Minnesota, which has 249 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04055844 being conducted?

This trial has 3 study locations across Minnesota, Missouri, New York. 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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