Expired Study
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Houston, Texas 77030


This randomized phase II trial is studying how well cilengitide works in treating patients with acute myeloid leukemia. Cilengitide may stop the growth of cancer cells by blocking the enzymes necessary for their growth

Study summary:

PRIMARY OBJECTIVES: I. Determine 10-month relapse-free survival of patients with acute myeloid leukemia in first complete remission treated with cilengitide as maintenance therapy. SECONDARY OBJECTIVES: I. Determine overall survival of patients treated with this drug. II. Determine the safety and toxicity of this drug in these patients. III. Determine the biological activity of this drug in cells from these patients. OUTLINE: This is a randomized study. Patients are randomized to 1 of 2 treatment arms. Arm I: Patients receive cilengitide IV at a lower dose over 1 hour twice weekly for 4 weeks. Arm II: Patients receive cilengitide IV at a higher dose over 1 hour twice weekly for 4 weeks. In both arms, courses repeat every 4 weeks in the absence of disease relapse or unacceptable toxicity.


Inclusion Criteria: - Diagnosis of acute myeloid leukemia (AML) - In first complete remission after at least 1 course of induction chemotherapy AND 1-2 courses of consolidation chemotherapy for newly diagnosed AML, as defined by the following: - No evidence of disease in bone marrow - Recovery of peripheral blood counts - Platelet count > 100,000/mm^3 - Absolute neutrophil count > 1,500/mm^3 - Must be able to start study medication within 60 days from the start of the last consolidation therapy - Must not have a suitable donor, refused, or ineligible for hematopoietic stem call transplantation - None of the following AML subtypes or chromosomal translocations: - Acute promyelocytic leukemia - t(8;21) - t(16;16) - inv(16) - Performance status - ECOG 0-2 - Performance status - Karnofsky 60-100% - See Disease Characteristics - Bilirubin ≤ 1.5 times upper limit of normal (ULN) - ALT ≤ 2.5 times ULN - Creatinine ≤ 1.5 times ULN - Creatinine clearance > 60mL/min - No symptomatic congestive heart failure - No unstable angina pectoris - No cardiac arrhythmia - Not pregnant or nursing - Negative pregnancy test - Fertile patients must use effective contraception - No ongoing or active infection - No psychiatric illness or social situation that would preclude study compliance - No other uncontrolled illness - No prior investigational agents specifically designated as an antiangiogenic agent - No concurrent prophylactic hematopoietic colony-stimulating factors - See Disease Characteristics - Recovered from prior consolidation chemotherapy - No other concurrent anticancer therapies - No other concurrent investigational cytotoxic agents



Primary Contact:

Principal Investigator
Srdan Verstovsek
M.D. Anderson Cancer Center

Backup Contact:


Location Contact:

Houston, Texas 77030
United States

There is no listed contact information for this specific location.

Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: November 18, 2019

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