VELCADE in Subjects With Relapsed or Refractory Mantle Cell Lymphoma

NCT ID: NCT00063713

Last Updated: 2008-02-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

152 participants

Study Classification

INTERVENTIONAL

Study Start Date

2003-06-30

Brief Summary

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The purpose of this study is to find out whether treatment with VELCADE will increase the time it takes for lymphoma to get worse.

Detailed Description

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VELCADE is approved in multiple myeloma for patients who have received two prior therapies and their disease came back or got worse while on their second therapy. VELCADE is currently being studied in other types of cancers.

Conditions

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Mantle Cell Lymphoma

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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VELCADE TM (bortezomib) for Injection

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* 18 years of age or older
* Confirmed diagnosis of mantle cell lymphoma
* Documented relapse or progressive disease following 1 or 2 prior lines of anti-cancer therapy. At least one of those regimens must have included an anthracycline or mitoxantrone. Relapsed or progressive disease, since last therapy must be documented by new lesions or objective evidence of the progression of existing lesions.
* At least 1 measurable or evaluable site of disease
* Voluntary consent

Exclusion Criteria

* Previous treatment with VELCADE
* Any experimental or anti-cancer therapy within 3 weeks before the first dose of study drug
* Radiation therapy within 3 weeks before the first dose of study drug
* Major surgery with 2 weeks before the first dose of study drug
* Rituximab, Campath, or other unconjugated therapeutic antibody within 4 weeks before the first dose of study drug
* Radioimmunotherapy or other toxin immunoconjugates such as Zevalin or Bexxar within 10 weeks before the first dose of study drug
* History of allergic reactions to boron or mannitol compounds
* Diagnosed or treated for another malignancy other than mantle cell lymphoma with 5 years before the first dose of study drug
* Active systemic infection requiring treatment
* Women patients must not be pregnant or breast-feeding, confirmed through pregnancy test obtained during screening (this test is not required for women who are post-menopausal or surgically sterile)
* Serious medical or psychiatric illness likely to interfere with participation in this clinical study
* Concurrent treatment with another investigational drug or participation in non-treatment studies is not allowed if it interferes with participation in this clinical study
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Millennium Pharmaceuticals, Inc.

INDUSTRY

Sponsor Role lead

Locations

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University of Alabama

Birmingham, Alabama, United States

Site Status

Alta Bates Medical Center

Berkeley, California, United States

Site Status

City of Hope Comprehensive Cancer Center

Duarte, California, United States

Site Status

Loma Linda Cancer Research Institute

Loma Linda, California, United States

Site Status

UCLA School of Medicine

Los Angeles, California, United States

Site Status

Stanford University

Palo Alto, California, United States

Site Status

University of Colorado Cancer

Denver, Colorado, United States

Site Status

Georgetown University Medical Center Lombardi Cancer Center

Washington D.C., District of Columbia, United States

Site Status

H. Lee Moffitt Cancer Center & Research Institute

Tampa, Florida, United States

Site Status

The Emory Clinic

Atlanta, Georgia, United States

Site Status

The Rush Cancer Center

Chicago, Illinois, United States

Site Status

University of Chicago Medical Center

Chicago, Illinois, United States

Site Status

Indiana University Cancer Center

Indianapolis, Indiana, United States

Site Status

University of Iowa Hospital Division

Iowa City, Iowa, United States

Site Status

North Memorial Hospital

Robbinsdale, Minnesota, United States

Site Status

Onc/Hem Associates of Kansas City

Kansas City, Missouri, United States

Site Status

University of Nebraska Medical Center

Omaha, Nebraska, United States

Site Status

Dartmouth-Hitchcock Medical Center

Lebanon, New Hampshire, United States

Site Status

Beth Israel Medical Center

New York, New York, United States

Site Status

St Lukes-Roosevelt Hospital

New York, New York, United States

Site Status

Memorial Sloan Kettering Cancer Center

New York, New York, United States

Site Status

New York Hospital Cornell Medical Center

New York, New York, United States

Site Status

University of Rochester Medical Center

Rochester, New York, United States

Site Status

University of North Carolina

Chapel Hill, North Carolina, United States

Site Status

Wake Forest, University health Sciences/Comprehensive Cancer Center

Winston-Salem, North Carolina, United States

Site Status

Cancer Care Associates

Oklahoma City, Oklahoma, United States

Site Status

Cancer Care Associates

Tulsa, Oklahoma, United States

Site Status

Oregon Health Science University

Portland, Oregon, United States

Site Status

University of Pennsylvania Cancer Center

Philadelphia, Pennsylvania, United States

Site Status

Fox Chase Cancer Center

Philadelphia, Pennsylvania, United States

Site Status

Western Pennsylvania Hospital

Pittsburgh, Pennsylvania, United States

Site Status

Vanderbilt University

Nashville, Tennessee, United States

Site Status

Sarah Cannon Cancer Center

Nashville, Tennessee, United States

Site Status

MD Anderson Cancer Center

Houston, Texas, United States

Site Status

University Hospital-Madison Wisconsin

Madison, Wisconsin, United States

Site Status

Countries

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United States

Other Identifiers

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M34103-053

Identifier Type: -

Identifier Source: org_study_id

NCT00084851

Identifier Type: -

Identifier Source: nct_alias

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