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Sponsored by: |
Amgen |
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Information provided by: | Amgen |
ClinicalTrials.gov Identifier: | NCT00044902 |
Epratuzumab is currently being studied in combination with rituximab, for the treatment of patients with low-grade NHL who failed previous chemotherapy and have never received rituximab or who received rituximab as a single agent or in combination with chemotherapy as their last treatment and who demonstrated a partial response or complete response for at least 12 months.
Condition | Intervention | Phase |
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Non-Hodgkin's Lymphoma |
Drug: epratuzumab |
Phase II |
Study Type: | Interventional |
Study Design: | Treatment |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Responsible Party: | Amgen Inc. ( Global Development Leader ) |
Study ID Numbers: | 20010138 |
Study First Received: | September 6, 2002 |
Last Updated: | December 20, 2007 |
ClinicalTrials.gov Identifier: | NCT00044902 History of Changes |
Health Authority: | United States: Food and Drug Administration |
Antibodies, Monoclonal Lymphoma, Small Cleaved-cell, Diffuse Lymphatic Diseases Antibodies Immunoproliferative Disorders |
Lymphoproliferative Disorders Lymphoma, Non-Hodgkin Lymphoma Immunoglobulins |
Lymphatic Diseases Neoplasms Immunoproliferative Disorders Neoplasms by Histologic Type |
Immune System Diseases Lymphoproliferative Disorders Lymphoma, Non-Hodgkin Lymphoma |