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Brief Title: Rituximab in Treating Patients With Hodgkin's Lymphoma
Official Title: Phase 2 Trial to Evaluate the Efficacy of Anti-CD20 Antibody in Patients With Lymphocyte Predominant Hodgkin's Disease
Study ID: NCT00003820
Brief Summary: Phase 2 trial to study the effectiveness of rituximab in treating patients who have lymphocyte-predominant Hodgkin's lymphoma.
Detailed Description: This study will evaluate the partial, complete, and overall response rates to rituximab of subjects with lymphocyte-predominant Hodgkin's lymphoma. Subjects will receive rituximab by IV infusion over several hours once a week for 4 weeks, followed by maintenance therapy as repeat course of the same dose and schedule rituximab at 6, 12, and 18 months. This was a single-arm study with multiple treatment periods added by amendment (ie, Secondary Group), with results reported by treatment period. As this was always considered a single-arm study, there was no intent to report the results for the initial treatment period separately as the Initial Group vs the Secondary Group.
Minimum Age: 3 Years
Eligible Ages: CHILD, ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Stanford University Medical Center, Stanford, California, United States
Stanford University School of Medicine, Stanford, California, United States
Name: Ranjana H Advani, MD
Affiliation: Stanford University
Role: STUDY_DIRECTOR
Name: Richard T Hoppe, MD
Affiliation: Stanford University
Role: PRINCIPAL_INVESTIGATOR