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Not listed Phase 2 Interventional

Rituxan Plus FavId (Idiotype Vaccine) for Low-grade Non-Hodgkin's Lymphoma

ClinicalTrials.gov ID: NCT00041730

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT00041730. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 14, 2026, 11:01 PM EST

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Official title

Phase II Trial of Rituxan(R) Plus FavId(TM) (Tumor-Specific Idiotype-KLH) and GM-CSF Immunotherapy in Patients With Grade 1 or 2 Follicular B-Cell Lymphoma

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate the ability of patients treated with Rituxan® plus FavId™ and GM-CSF to mount an immune response (humoral and/or cellular) to KLH and their idiotype.

Study identification

NCT ID
NCT00041730
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Favrille
Industry
Enrollment
90 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 2002 (Type not available)
Primary completion
Not listed
Completion
Not listed
Last update posted
Sep 30, 2009

Started 2002

United States locations

U.S. sites
15
U.S. states
9
U.S. cities
15
Facility City State ZIP Site status
University of California, San Diego La Jolla California 92093 —
Tower Hematology Oncology Medical Group Los Angeles California 90048 —
Oncology Associates of San Diego San Diego California 92123 —
University California, San Francisco San Francisco California 94143 —
University of Florida, Jacksonville Jacksonville Florida 32209 —
H. Lee Moffitt Cancer Center Tampa Florida 33612 —
Northwestern University Chicago Illinois 60611 —
Ochsner Clinical Foundation New Orleans Louisiana 70121 —
Henry Ford Hospital Detroit Michigan 48202 —
New York Medical College - Our Lady of Mercy Medical Center, Comprehensive Cancer Center The Bronx New York 10466 —
Oncology/Hematology Care Clinical Cancer Institute Cincinnati Ohio 45219 —
University Hospitals of Cleveland Case Western, Ireland Cancer Center Cleveland Ohio 44106 —
The Ohio State University Columbus Ohio 43210 —
The Sarah Cannon Cancer Center Nashville Tennessee 37203 —
University of Virginia Charlottesville Virginia 22902 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00041730, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 30, 2009 · Synced Nov 14, 2026

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