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Completed Phase 2 Interventional

Amonafide in Combination With Cytarabine in Secondary AML

ClinicalTrials.gov ID: NCT00273884

Public ClinicalTrials.gov record NCT00273884. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 12:32 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase 2 Open-Label Study of Amonafide L-Malate in Combination With Cytarabine in Subjects With Secondary Acute Myeloid Leukemia (AML)

Study identification

NCT ID
NCT00273884
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Xanthus Pharmaceuticals, Inc.
Industry
Enrollment
80 participants

Conditions and interventions

Interventions

  • Amonafide L-Malate Drug
  • Cytarabine Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 31, 2005
Primary completion
Not listed
Completion
Mar 31, 2009
Last update posted
Feb 18, 2007

2005 – 2009

United States locations

U.S. sites
19
U.S. states
15
U.S. cities
19
Facility City State ZIP Site status
University of Alabama at Birmingham Comprehensive Cancer Center Birmingham Alabama 35294-3300
City of Hope National Medical Center Duarte California 91010
UCLA Medical Center Los Angeles California 90024
Scripps Cancer Center San Diego California 92121
University of Colorado Health Sciences Center, Anschutz Cancer Center Aurora Colorado 80010
University of Florida Health Science Center Gainesville Florida 32610-0277
Northwestern University, Robert H. Lurie Comprehensive Cancer Center Chicago Illinois 60611
St. Francis Cancer Research Foundation (formerly Indiana Oncology Hematology Consultants and American Health Network of Indiana LLC, Oncology Division) Indianapolis Indiana 46202
Dana Farber Cancer Institute Boston Massachusetts 02115
University of Massachusetts Memorial Medical Center Worcester Massachusetts 01655
University of Michigan Ann Arbor Michigan 48109-0848
University of Nebraska Medical Center Omaha Nebraska 98198 7835
Roswell Park Cancer Institute Buffalo New York 75246
Duke University Medical Center Durham North Carolina 27710
Wake Forest University Health Sciences Winston-Salem North Carolina 27157
MUSC - Hollings Cancer Center Charleston South Carolina 29425
Baylor University Medical Center Dallas Texas 75246
West Virginia University Medical Center Morgantown West Virginia 26506-9162
Medical College of Wisconsin Milwaukee Wisconsin 53226

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00273884, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 18, 2007 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00273884 live on ClinicalTrials.gov.

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