Non Hodgkin Lymphoma Clinical Trial

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Feasibility Study of a 60 Minute Rapid Infusion Rituximab Protocol in Patients With B-cell Malignancies

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Summary

The purpose of this study is to assess the feasibility of a 60 minute rapid infusion rituximab protocol in the institution's outpatient infusion center.

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Eligibility Criteria

Inclusion Criteria:

Age 18-89
Diagnosis of indolent or intermediate grade B-cell malignancy
Patients receiving rituximab-based therapy at a dose of 375mg/m2, regardless of weight
First dose given within 3 months of the second dose
Infusion scheduled for outpatient administration at The Arthur G. James Cancer Hospital and Richard J. Solove Research Institute

Exclusion Criteria:

Diagnosis of aggressive lymphoma
Absolute lymphocyte count > 10 x 103 cells/µL
New York Heart Association (NYHA) classification Grade II or greater congestive heart failure
Enrolled on another clinical trial
Allergy to murine-containing medications
Grade III or IV hypersensitivity reaction during the initial infusion of rituximab
Prisoners
Pregnant women
Mentally or physically unable to give consent

Study is for people with:

Non Hodgkin Lymphoma

Phase:

Phase 2

Estimated Enrollment:

52

Study ID:

NCT01206777

Recruitment Status:

Completed

Sponsor:

Ohio State University Comprehensive Cancer Center

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There is 1 Location for this study

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The Ohio State University Comprehensive Cancer Center
Columbus Ohio, 43210, United States

How clear is this clinincal trial information?

Study is for people with:

Non Hodgkin Lymphoma

Phase:

Phase 2

Estimated Enrollment:

52

Study ID:

NCT01206777

Recruitment Status:

Completed

Sponsor:


Ohio State University Comprehensive Cancer Center

How clear is this clinincal trial information?

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