Trial Search Results

MLN4924 for the Treatment of Acute Myelogenous Leukemia, Myelodysplastic Syndrome, and Acute Lymphoblastic Leukemia

An open-label, multicenter, phase 1, dose escalation study of MLN4924 in adult patients with acute myelogenous leukemia (AML), high-grade myelodysplastic syndrome (MDS). The patient population will consist of adults previously diagnosed with AML including high-grade MDS for which standard curative, life-prolonging treatment does not exist or is no longer effective.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Millennium Pharmaceuticals, Inc.

Stanford Investigator(s):

Intervention(s):

  • Drug: MLN4924
  • Drug: Azacitidine

Phase:

Phase 1

Eligibility


Inclusion Criteria:

   - Age greater than or equal to 18 years

   - Have the following diagnosis:

      - AML or ALL (for the dose escalation phase only)including leukemia secondary to
      prior chemotherapy or resulting from an antecedent hematologic disorder, who have
      failed to achieve complete response (CR) or who have relapsed after prior therapy
      and are not candidates for potentially curative treatment.

      - Acute Promyelocytic Leukemia (APL) patients are not eligible

      - AML or ALL patients who are over age 60 and have not received prior therapy are
      also eligible if they are not candidates for standard induction chemotherapy

      - High-grade MDS, defined as > 10% blasts on bone marrow examination

      - Low-grade MDS, defined as < 10% blasts on bone marrow examination (Schedule B
      expansion cohort only)

   - Patients who are willing to refrain from donating blood for at least 90 days after
   their final dose of MLN4924 and (for male patients) willing to refrain from donating
   semen for at least 4 months after their final dose of MLN4924

   - Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2

   - Female patients who are postmenopausal, surgically sterile, or agree to practice 2
   effective methods of contraception or abstain from heterosexual intercourse

   - Male patients who agree to practice 2 effective methods of contraception or abstain
   from heterosexual intercourse

   - Voluntary written consent

   - Suitable venous access

   - Adequate clinical laboratory values during the screening period as specified in the
   protocol

   - Patients who are on hydroxyurea may be included in the study and may continue on
   hydroxyurea while participating in this study.

Exclusion Criteria:

   - Female patients who are lactating or have a positive serum pregnancy test during the
   screening period

   - Any serious medical or psychiatric illness

   - Treatment with any investigational products

   - Systemic antineoplastic therapy or radiotherapy within 14 days before the first dose
   of study drug, except for hydroxyurea

   - Major surgery within 14 days before the first dose of study drug

   - Life-threatening illness unrelated to cancer

   - Clinically uncontrolled central nervous system (CNS) involvement

   - Known human immunodeficiency virus (HIV) positive

   - Known hepatitis B surface antigen-positive, or known or suspected active hepatitis C
   infection

   - Evidence of uncontrolled cardiovascular conditions as specified in the protocol

   - Diarrhea > Grade 1, based on the NCI CTCAE categorization

   - Systemic treatment with prohibited medications

   - Ongoing anticoagulant therapy (eg, aspirin, Coumadin, heparin) that cannot be held to
   permit bone marrow sampling

   - Use of acetaminophen, acetaminophen-containing products, and statins are not permitted
   on the day before dosing, day of dosing, and day after dosing with MLN4924

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Cancer Clinical Trials Office
650-498-7061
Not Recruiting