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Proleukin in Combination With Rituxan in Patients With Intermediate and High-Grade Non-Hodgkin's Lymphoma.

Phase 2
Completed
Conditions
Lymphoma, Non-Hodgkin
Registration Number
NCT00045864
Lead Sponsor
Chiron Corporation
Brief Summary

The purpose of this study is to determine the safety and effectiveness of combination therapy with Proleukin and Rituxan on patients with intermediate-and high- grade Non-Hodgkin's lymphoma.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (33)

ACRC/Arizona Clinical Research Center, Inc.

🇺🇸

Tucson, Arizona, United States

Hoag Cancer Center

🇺🇸

Newport Beach, California, United States

UC Davis Cancer Center

🇺🇸

Sacramento, California, United States

John Wayne Cancer Institute

🇺🇸

Santa Monica, California, United States

Stanford University Medical Center

🇺🇸

Stanford, California, United States

California Cancer Medical Center

🇺🇸

West Covina, California, United States

Georgetown University Medical Center, Lombardi Cancer Center

🇺🇸

Washington, District of Columbia, United States

Washington Cancer Institute

🇺🇸

Washington, District of Columbia, United States

Division of Hematology/Oncology, University of Miami School of Medicine

🇺🇸

Miami, Florida, United States

Northwestern University, Feinberg School of Medicine

🇺🇸

Chicago, Illinois, United States

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ACRC/Arizona Clinical Research Center, Inc.
🇺🇸Tucson, Arizona, United States

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