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Terminated Phase 2 Interventional Results available

Comparison Study of Rituximab Plus Sargramostim to Rituximab Alone for Relapsed Follicular B-cell Lymphoma, a Form of Non-Hodgkin's Lymphoma

ClinicalTrials.gov ID: NCT00308087

Public ClinicalTrials.gov record NCT00308087. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 16, 2026, 11:55 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Randomized, Open Label, Phase II Trial Comparing Rituximab Plus Sargramostim to Rituximab Monotherapy for the Treatment of Relapsed 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 whether treatment with rituximab plus sargramostim will be more effective than rituximab alone.

Study identification

NCT ID
NCT00308087
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Genzyme, a Sanofi Company
Industry
Enrollment
75 participants

Conditions and interventions

Interventions

Drug

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
Apr 30, 2006
Primary completion
May 31, 2009
Completion
May 31, 2009
Last update posted
Dec 26, 2013

2006 – 2009

United States locations

U.S. sites
21
U.S. states
10
U.S. cities
21
Facility City State ZIP Site status
Not listed Birmingham Alabama 35234
Not listed Huntsville Alabama 35805
Not listed Los Angeles California 90095
Not listed Montebello California 90640
Not listed Pleasant Hill California 94523
Not listed Gainesville Florida 32610-0254
Not listed Jacksonville Florida 32207
Not listed Ocala Florida 34474
Not listed Tampa Florida 33612
Not listed Chicago Illinois 60612
Not listed Elk Grove Village Illinois 60007
Not listed Springfield Illinois 62703
Not listed Indianapolis Indiana 46202
Not listed New Albany Indiana 47150
Not listed Duluth Minnesota 55805-1984
Not listed Fresh Meadows New York 11365
Not listed New York New York 10019
Not listed Columbus Ohio 43235
Not listed Hershey Pennsylvania 17033-0850
Not listed Philadelphia Pennsylvania 19104
Not listed Houston Texas 77030

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00308087, 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 Dec 26, 2013 · Synced Sep 16, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00308087 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →