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Study Title: SWOG S0016
Category: Cancer, General

Currently accepting participants?
Yes - please read the description below and contact the study coordinator if you are interested.

Principal Investigator: Jacqueline Vuky
Study Coordinator: Kathy Rabena
Phone: (206) 223-6892 Ext.36892
Email: hemkcr@vmmc.org

What is the SWOG S0016 study?

Arm 1: CHOP (Cyclophosphamide, Doxorubicin, Predinison, Vincristine) + Rituximab Arm 2: CHOP + Tositumomab + I-131 Tositumomab

Who can participate?

Eligibiligy:
~Untreated Follicular Non-Hodgkin's Lymphoma
~Lymphoma must express CD20 antigen
~Must have bidemensional measurable disease
~Must have Stage III, Stage IV or bulky Stage II

Ineligibilty:
~Must not be HIV positive
~Pregnant or nursing women are ineligible
~No prior malignancy within the last 5 years

What do I have to do as a study participant?

Study Summary:

"A Phase II Trial of Chop + RItuximan vs. Chop+ iodine-131-Labeled Monoclonal Anti-B1 Antibody (Tositumomab) for Treatemtn of Newly Diagnosed Follicular Non-Hodgkin's Lymphomas"

Detailed Study Description:

(No information)

Study Design: Interventional
Phase of Study: Phase III
Study Type: Interventional
Condition or Study Focus: Follicular Non-Hodgkin's Lymphoma
Intervention Type: Monoclonal Antibody
Intervention Name: Tositumomab
Gender: Male and Female
Age group: Interventional
Sponsor: Southwest Oncology Group (SWOG)


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