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Spots Global Cancer Trial Database for Treatment of Relapsed Low-Grade or Follicular Lymphoma With Rituximab (Also Known as Rituxan, IDEC-C2B8, IDEC-102)

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Treatment of Relapsed Low-Grade or Follicular Lymphoma With Rituximab (Also Known as Rituxan, IDEC-C2B8, IDEC-102)

Official Title: Pivotal Phase III Multi-Center Study to Evaluate the Safety and Efficacy of Once Weekly Times Four Dosing of IDEC-C2B8 (IDEC-102) in Patients With Relapsed Low-Grade or Follicular B-Cell Lymphoma

Study ID: NCT00168740

Interventions

rituximab

Study Description

Brief Summary: Rituximab is an antibody made in a laboratory. It binds to lymphoma cells and kills them. Treatment of recurrent B-cell lymphoma with rituximab may delay or prevent relapses. A total of 166 patients with recurrent B-cell lymphoma were given intravenous rituximab once a week for 4 weeks. The patients' tumors were measured before and after treatment. Ten patients had a complete response and 70 patients had a partial response to rituximab. The median duration of response was 11.2 months.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of Arkansas for Medical Sciences, Little Rock, Arkansas, United States

City of Hope Natioal Medical Center, Duarte, California, United States

Scripps Memorial Hospital, La Jolla, California, United States

UCSD Stem Cell Laboratory, La Jolla, California, United States

Hoag Hospital, Newport Beach, California, United States

Sutter Cancer Center, Sacramento, California, United States

Sidney Kimmel Cancer Center, San Diego, California, United States

University of California, San Francisco, San Francisco, California, United States

Stanford University Medical Center, Stanford, California, United States

Kaiser Permanente Medical Center, Vallejo, California, United States

Rocky Mountain Cancer Center, Denver, Colorado, United States

Georgetown University Medical Center, Washington, District of Columbia, United States

Robert H. Lurie Cancer Center, Northwestern University, Chicago, Illinois, United States

University of Iowa General Hospital, Iowa City, Iowa, United States

University of Kentucky Medical Center, Lexington, Kentucky, United States

Louisiana State University, Shreveport, Louisiana, United States

University of Maryland Cancer Center, Baltimore, Maryland, United States

Michigan State University, East Lansing, Michigan, United States

St. Louis University Medical Center, St. Louis, Missouri, United States

Roswell Park Cancer Center, Buffalo, New York, United States

University of Rochester Cancer Center, Rochester, New York, United States

Fox Chase Cancer Center, Philadelphia, Pennsylvania, United States

University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States

The West Clinic, P.C., Memphis, Tennessee, United States

Texas Oncology, P.A., Dallas, Texas, United States

M.D. Anderson Cancer Center, Houston, Texas, United States

University of Texas Health Sciences Center, San Antonio, Texas, United States

University of Virginia, Charlottesville, Virginia, United States

Fred Hutchinson Cancer Research Center, Seattle, Washington, United States

Ottawa General Hospital, Ottawa, Ontario, Canada

Toronto-Sunnybrook Regional Cancer Center, Toronto, Ontario, Canada

Contact Details

Name: Antonio J. Grillo-Lopez, M.D.

Affiliation: Biogen

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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