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NCT00986804 · ClinicalTrials.gov registry record · Phase 1

Decitabine Maintenance for Acute Myelogenous Leukemia (AML) and Myelodysplastic Syndrome (MDS) Post Transplant

A Phase 1 study of Myelodysplastic Syndromes and Leukemia, Myeloid, Acute, sponsored by Washington University School of Medicine.

Completed
Registry status
Phase 1
Development phase
24
Enrollment target
1
Study location

NCT00986804 is a Phase 1 study of Myelodysplastic Syndromes and Leukemia, Myeloid, Acute that has completed, run by Washington University School of Medicine. The registered enrollment target is 24 participants, below the 285-participant average among 173 other Myelodysplastic Syndromes trials with a reported enrollment target (92% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00986804, a Phase 1 study of Myelodysplastic Syndromes and Leukemia, Myeloid, Acute, has completed, sponsored by Washington University School of Medicine.

COMPLETED
Registry status
Phase 1
Development phase
24 participants
Enrollment target
1
Study location

Study Summary

Primary: To determine the maximum tolerated dose and schedule of decitabine when administered as maintenance therapy after allogeneic hematopoietic stem cell transplantation (alloHSCT) performed for AML or high-risk MDS.

Interventions

  • DRUG Decitabine

Study Locations (1)

Missouri

  • Washington University School of Medicine - St Louis

Trial Details

FieldValue
Enrollment Target 24 participants
Start Date 2009-12
Est. Completion 2016-02
Phase Phase 1

What the Registry Record Tells You About NCT00986804

The ClinicalTrials.gov registry entry for NCT00986804 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 24 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 (92% 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 2 conditions, with Myelodysplastic Syndromes appearing as the primary indexed condition, and to 1 intervention - of which Decitabine is the first listed.

NCT00986804 reports 1 study location spanning 1 distinct geographic area - top geographies include Missouri.

Frequently Asked Questions

What is clinical trial NCT00986804 about?

NCT00986804 is a clinical study titled "Decitabine Maintenance for Acute Myelogenous Leukemia (AML) and Myelodysplastic Syndrome (MDS) Post Transplant". Primary: To determine the maximum tolerated dose and schedule of decitabine when administered as maintenance therapy after allogeneic hematopoietic stem cell transplantation (alloHSCT) performed for AML or high-risk MDS.

What is the current status of trial NCT00986804?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 24 participants. The study started on 2009-12. Estimated completion is 2016-02.

What conditions does trial NCT00986804 study?

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

What interventions are being tested in trial NCT00986804?

The interventions under investigation include: Decitabine (DRUG).

Who is sponsoring clinical trial NCT00986804?

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

Where is trial NCT00986804 being conducted?

This trial has 1 study location across Missouri. 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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