Completed

VNP40101M in Treating Patients With Acute Myelogenous Leukemia or High-Risk Myelodysplasia

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What is being tested

hydroxyurea

+ laromustine
Drug
Who is being recruted

Leukemia

+ Myelodysplastic Syndromes
+ Myelodysplastic/Myeloproliferative Neoplasms
Over 18 Years
How is the trial designed

Treatment Study

Phase 2
Interventional
Study Start: November 2005

Summary

Principal SponsorVion Pharmaceuticals
Last updated: July 18, 2013
Sourced from a government-validated database.Claim as a partner
Study start date: November 1, 2005Actual date on which the first participant was enrolled.

RATIONALE: Drugs used in chemotherapy, such as VNP40101M and hydroxyurea, work in different ways to stop cancer cells from dividing so they stop growing or die. Hydroxyurea may help VNP40101M kill more cancer cells by making cancer cells more sensitive to the drug. PURPOSE: This phase II trial is studying how well giving VNP40101M with hydroxyurea works in treating patients with acute myelogenous leukemia or high-risk myelodysplasia. OBJECTIVES: * Determine the complete response rate to VNP40101M in patients with acute myelogenous leukemia or high-risk myelodysplasia . * Determine the toxic effects of this regimen in these patients. * Determine the pharmacokinetics of this regimen in these patients. OUTLINE: This is an open-label, multicenter study. Patients are stratified to acute myelogenous leukemia (AML) or high risk myelodysplasia (MDS) patients ≥ 60 years old with no prior treatment vs AML patients any age in first relapse. (AML patients any age in first relapse closed to accrual 06/09/05). Patients receive VNP40101M IV over 30 minutes once on day 1 (course 1). Four to five weeks after the first course, patients undergo bone marrow aspiration and biopsy. If the bone marrow is improved but contains residual leukemia, patients receive a second course of VNP40101M (at the same dose as in course 1). If patients achieve complete response (CR), or partial CR after the first or second course, a consolidation course may be given comprising VNP40101M at a reduced dose. Patients are followed monthly for 6 months, every 2 months for 12 months, and then every 3 months for 18 months . PROJECTED ACCRUAL: A total of 230 patients (100 with acute myelogenous leukemia (AML) or high-risk myelodysplasia and 130 with AML in first relapse) will be accrued for this study.

Official TitleA Phase II Study of VNP40101M For Patients With Acute Myelogenous Leukemia Or High-Risk Myelodysplasia 
Principal SponsorVion Pharmaceuticals
Last updated: July 18, 2013
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details
230 patients to be enrolledTotal number of participants that the clinical trial aims to recruit.
Treatment Study
These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.

How the interventions assigned to participants is kept confidential
Everyone involved in the study knows which treatment is being given. This is typically used when it's not possible or necessary to hide the treatment details from participants or researchers.

Other Ways to Mask Information
Single-blind
: Participants do not know which treatment they are receiving, but researchers do.

Double-blind
: Neither participants nor researchers know which treatment is given.

Triple-blind
: Participants, researchers, and outcome assessors do not know which treatment is given.

Quadruple-blind
: Participants, researchers, outcome assessors, and care providers all do not know which treatment is given.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria
Any sexBiological sex of participants that are eligible to enroll.
Over 18 YearsRange of ages for which participants are eligible to join.
Healthy volunteers not allowedIf individuals who are healthy and do not have the condition being studied can participate.
Conditions
Pathology
Leukemia
Myelodysplastic Syndromes
Myelodysplastic/Myeloproliferative Neoplasms
Criteria

DISEASE CHARACTERISTICS: * Histologically confirmed diagnosis of 1 of the following: * Acute myelogenous leukemia (AML), meeting the following criteria: * In first relapse after first treatment-induced complete remission (CR) (closed to accrual as of 06/09/05) * Duration of first CR less than 12 months * No prior treatment for first relapse except hydroxyurea * FAB type M0, M1, M2, M4-7 * No acute promyelocytic leukemia * No prior treatment with a standard induction regimen containing cytotoxic agents\* (for patients 60 years of age or older) * High-risk myelodysplasia, meeting the following criteria: * 60 years of age and over * No prior cytotoxic chemotherapy\* except hydroxyurea * Prior gemtuzumab ozogamicin allowed * High risk defined as International Prognostic Scoring System score ≥ 1.5, defined by cytogenetics, % marrow blasts, and lineage cytopenias NOTE: \*Prior low-dose, single-agent cytarabine, decitabine, or azacitidine not considered prior cytotoxic chemotherapy PATIENT CHARACTERISTICS: Age * 18 and over Performance status * ECOG 0-2 Life expectancy * Not specified Hematopoietic * Not specified Hepatic * Bilirubin ≤ 2.0 mg/dL * ALT or AST ≤ 5 times upper limit of normal * Chronic hepatitis allowed Renal * Creatinine ≤ 2.0 mg/dL Cardiovascular * No myocardial infarction within the past 3 months * No symptomatic coronary artery disease * No uncontrolled arrhythmias * No uncontrolled congestive heart failure * No other active heart disease Other * No uncontrolled active infection * Not pregnant or nursing * Fertile patients must use effective contraception PRIOR CONCURRENT THERAPY: Biologic therapy * Up to 4 leukapheresis procedures allowed during the first 15 days of study treatment Chemotherapy * See Disease Characteristics * Concurrent additional hydroxyurea (maximum dose of 5 g daily for up to 4 days) allowed between days 4 and 15 of each study course to control elevated blast levels Endocrine therapy * Not specified Radiotherapy * Not specified Surgery * Not specified Other * Recovered from all prior therapy * At least 72 hours since prior anti-leukemic treatment with a non-cytotoxic agent * No concurrent disulfiram (Antabuse) * No other concurrent anticancer drugs except anagrelide within the first 15 days of study treatment to control elevated platelet counts * No other concurrent treatment for leukemia, except hydroxyurea used during study treatment * No other concurrent investigational drugs


Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives
Study Objectives
Primary Objectives


Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.
This study has 5 locations
Suspended
Sidney Kimmel Comprehensive Cancer Center at Johns HopkinsBaltimore, United StatesSee the location
Suspended
Duke Comprehensive Cancer CenterDurham, United States
Suspended
M.D. Anderson Cancer Center at University of TexasHouston, United States
Suspended
Marseille Institute of Cancer - Institut J. Paoli and I. CalmettesMarseille, France

Completed5 Study Centers