A Phase 2 Study of Tandutinib in Patients With Newly Diagnosed Acute Myelogenous Leukemia Who Are Considered Ineligible For or Who Decline Treatment With Standard Induction Therapy

NCT00297921 | Withdrawn Phase 1

• 1 other identifier: C03002
• Study Type: interventional
• Target: N/A
• Locations: 0 countries
• Sites: N/A

Brief Summary

Prospective, nonrandomized, noncomparative, open-label, multicenter, 2-stage clinical study designed to determine the overall response (combined complete remission, complete remission with incomplete blood count recovery, partial remission, or blast response) rate following tandutinib therapy in 2 groups of patients with newly diagnosed Acute Myelogenous Luekemia.

Conditions

Acute Myelogenous Leukemia

Interventions

tandutinib DRUG

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Male or female, at least 18 years of age
• Unequivocal histologic or cytologic diagnosis of AML (based on the WorldHealth Organization \[WHO\] and/or FAB classifications), excluding acute promyelocytic leukemia (FAB M3).
• AML patients with a history of antecedent MDS or MPD are eligible for treatment in this study.
• In the opinion of the investigator is ineligible for or has declined treatment with standard induction therapy
• ECOG performance status of equal to or less then 3
• Ability to voluntarily provide written informed consent
• Determination of the presence or absence of a FLT3-ITD mutation before enrollment once it is ascertained that determination of FLT3-ITD mutation status is required to avoid exceeding enrollment in either patient group

You may not qualify if:

• Presence of an active malignancy other than AML at the time of study entry
• Documented or suspected central nervous system leukemia involvement
• Known gastrointestinal disease that could interfere with the absorption of oral tandutinib
• Severe central nervous system, pulmonary, renal, or hepatic disease not related to AML
• Myocardial infarction within 6 months of enrollment or New York Heart Association (NYHA) Class III or Class IV heart failure, uncontrolled angina, severe uncontrolled ventricular arrhythmias, or ECG evidence of acute ischemia or active conduction system abnormalities
• QTc \>500 milliseconds (ms)
• Family history of or congenital QTc prolongation
• Pretreatment laboratory test values as follows:
• Total bilirubin \>2.5 x the upper limit of normal (ULN)
• Alanine aminotransferase (ALT) \>2.5 x the ULN
• Serum creatinine \>4.0 mg/dL
• Known or suspected infection with human immunodeficiency virus
• Known active infection with hepatitis B or hepatitis C
• Known or suspected primary muscular or neuromuscular disease (eg, muscular dystrophy or myasthenia gravis)
• Receipt of prior antineoplastic therapy for leukemia, except that prior therapy with the following is allowed:

Sponsors & Collaborators

• Millennium Pharmaceuticals, Inc.: lead

MeSH Terms

Conditions

Leukemia, Myeloid, Acute

Interventions

tandutinib

Condition Hierarchy (Ancestors)

Leukemia, Myeloid; Leukemia; Neoplasms by Histologic Type; Neoplasms; Hematologic Diseases; Hemic and Lymphatic Diseases

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NON RANDOMIZED
• Masking: NONE
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY

Study Record Dates

• First Submitted: February 27, 2006
• First Posted: March 1, 2006
• Last Updated: November 6, 2013

Record last verified: 2013-11