Status:
COMPLETED
Study of VELCADE® With Mitoxantrone and Etoposide for Leukemias
Lead Sponsor:
Sidney Kimmel Cancer Center at Thomas Jefferson University
Collaborating Sponsors:
Millennium Pharmaceuticals, Inc.
Conditions:
Relapsed Acute Leukemia
Refractory Acute Leukemia
Eligibility:
All Genders
18+ years
Phase:
PHASE1
PHASE2
Brief Summary
Based on what is known about it's mechanism of action, bortezomib is presumed to make other chemotherapy drugs work better. This study examines the use of bortezomib in combination with an already eff...
Detailed Description
VELCADE is a drug that blocks growth of cancer cells and helps destroy them. This research will help us to determine if VELCADE when combined with chemotherapy is useful in treating the leukemia with ...
Eligibility Criteria
Inclusion
- Female subject is either post-menopausal or surgically sterilized or willing to use an acceptable method of birth control (ie, a hormonal contraceptive, intra-uterine device, diaphragm with spermicide, condom with spermicide, or abstinence) for the duration of the study.
- Male subject agrees to use an acceptable method for contraception for the duration of the study.
- Patients who have had a diagnosis of Acute Myeloid Leukemia (AML) or Acute Lymphoblastic Leukemia (ALL) will be eligible for the study.
- Patients must have failed initial therapy that may manifest in either of the following ways:
- Demonstration of Primary Refractory Disease (Primary Induction Failure) as evidenced by a mid-cycle bone marrow analysis showing lack of complete tumor clearance (CTC).
- Relapse of initial disease after a period of attaining complete remission.
- Patients must be \> 18 years of age, with no upper age limit.
- ECOG performance status of 0 or 1.
- Patients have no symptomatic cardiac or pulmonary disease and adequate hepatic and renal function as measured by the following criteria:
- Cardiac: Left ventricular ejection fraction at rest must be \>40% (MUGA preferred)
- Hepatic: ALT and AST \< 3x the upper limits of normal range as specified by the institution's clinical laboratory.
- Renal: Serum creatinine within the normal range (\< 1.4 mg/dL) or if creatinine outside normal range then creatinine clearance \> 60 mL/min/m2
- Patients who have had a diagnosis of Acute Myeloid Leukemia (AML) or Acute Lymphoblastic Leukemia (ALL) will be eligible for the study.
- Patients must have failed initial therapy that may manifest in either of the following ways:
- Demonstration of Primary Refractory Disease (Primary Induction Failure) as evidenced by a mid-cycle bone marrow analysis showing lack of complete tumor clearance (CTC).
- Relapse of initial disease after a period of attaining complete remission.
- Patients must be \> 18 years of age, with no upper age limit.
- ECOG performance status of 0 or 1.
- Patients have no symptomatic cardiac or pulmonary disease and adequate hepatic and renal function as measured by the following criteria:
- Cardiac: Left ventricular ejection fraction at rest must be \>40% (MUGA preferred)
- Hepatic: ALT and AST \< 3x the upper limits of normal range as specified by the institution's clinical laboratory.
- Renal: Serum creatinine within the normal range (\< 1.4 mg/dL) or if creatinine outside normal range then creatinine clearance \> 60 mL/min/m2
Exclusion
- Patient has \> Grade 2 peripheral neuropathy within 14 days before enrollment.
- Myocardial infarction within 6 months prior to enrollment or has New York Hospital Association (NYHA) Class III or IV heart failure (see section 8.4), uncontrolled angina, severe uncontrolled ventricular arrhythmias, or electrocardiographic evidence of acute ischemia or active conduction system abnormalities. Prior to study entry, any ECG abnormality at screening has to be documented by the investigator as not medically relevant.
- Patient has hypersensitivity to bortezomib, boron or mannitol.
- Female subject is pregnant or breast-feeding. Confirmation that the subject is not pregnant must be established by a negative serum or urinary pregnancy test result obtained during screening. Pregnancy testing is not required for post-menopausal or surgically sterilized women.
- Patient has received other investigational drugs within 14 days before enrollment
- Serious medical or psychiatric illness likely to interfere with participation in this clinical study.
Key Trial Info
Start Date :
January 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2014
Estimated Enrollment :
55 Patients enrolled
Trial Details
Trial ID
NCT00410423
Start Date
January 1 2006
End Date
September 1 2014
Last Update
April 30 2025
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Sidney Kimmel Cancer Center at Thomas Jefferson University
Philadelphia, Pennsylvania, United States, 19107