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NCT00041990 · ClinicalTrials.gov registry record · Phase 2

Phase II Trial of Decitabine in Patients With Chronic Myelogenous Leukemia Accelerated Phase Who Are Refractory to Imatinib Mesylate (Gleevec)

A Phase 2 study of Chronic Myelogenous Leukemia, sponsored by Astex Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
40
Enrollment target
8
Study locations

NCT00041990 is a Phase 2 study of Chronic Myelogenous Leukemia that has completed, run by Astex Pharmaceuticals. The registered enrollment target is 40 participants, below the 281-participant average among 29 other Chronic Myelogenous Leukemia trials with a reported enrollment target (86% lower). The trial reports 8 study locations across 6 states.

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The verdict

NCT00041990, a Phase 2 study of Chronic Myelogenous Leukemia, has completed, sponsored by Astex Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
40 participants
Enrollment target
8
Study locations

Study Summary

To determine the safety and efficacy of decitabine in patients with Philadelphia chromosome-positive chronic myelogenous leukemia accelerated phase that were previously treated with imatinib mesylate (STI 571) and became resistant/refractory or were found to be intolerant to the drug.

Interventions

  • DRUG decitabine (5-aza-2'deoxycytidine)

Study Locations (8)

California

  • City of Hope Medical Center - Duarte
  • Scripps Clinic - Escondido
  • USC/Norris Cancer Center - Los Angeles

Minnesota

  • Metro-Minnesota CCOP - Saint Louis Park

New York

  • New York Medical College - Valhalla

South Carolina

  • Liberty Hematology/Oncology - Columbia

Texas

  • University of Texas MD Anderson Cancer Center - Houston

Ontario

  • Princess Margaret Hospital - Toronto

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2002-07
Phase Phase 2

Sponsor

Astex Pharmaceuticals

38 total trials

What the Registry Record Tells You About NCT00041990

The ClinicalTrials.gov registry entry for NCT00041990 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 281-participant average among 29 other Chronic Myelogenous Leukemia trials with a reported enrollment target (86% lower). The listed sponsor is Astex Pharmaceuticals, which has 38 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Chronic Myelogenous Leukemia appearing as the primary indexed condition, and to 1 intervention - of which decitabine (5-aza-2'deoxycytidine) is the first listed.

NCT00041990 reports 8 study locations spanning 6 distinct geographic areas - top geographies include California, Minnesota, New York.

Frequently Asked Questions

What is clinical trial NCT00041990 about?

NCT00041990 is a clinical study titled "Phase II Trial of Decitabine in Patients With Chronic Myelogenous Leukemia Accelerated Phase Who Are Refractory to Imatinib Mesylate (Gleevec)". To determine the safety and efficacy of decitabine in patients with Philadelphia chromosome-positive chronic myelogenous leukemia accelerated phase that were previously treated with imatinib mesylate (STI 571) and became resistant/refractory or were found to be intolerant to the drug.

What is the current status of trial NCT00041990?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 40 participants. The study started on 2002-07.

What conditions does trial NCT00041990 study?

This clinical trial studies the following conditions: Chronic Myelogenous Leukemia.

What interventions are being tested in trial NCT00041990?

The interventions under investigation include: decitabine (5-aza-2'deoxycytidine) (DRUG).

Who is sponsoring clinical trial NCT00041990?

This trial is sponsored by Astex Pharmaceuticals, which has 38 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00041990 being conducted?

This trial has 8 study locations across California, Minnesota, New York, South Carolina, Texas. 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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.