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Spots Global Cancer Trial Database for Comparative Trial for Pixantrone in Combination With Rituximab in Indolent Non-Hodgkin's Lymphoma

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Trial Identification

Brief Title: Comparative Trial for Pixantrone in Combination With Rituximab in Indolent Non-Hodgkin's Lymphoma

Official Title: An Open-Label, Randomized, Phase III Comparative Trial of BBR 2778 + Rituximab Versus Rituximab in the Treatment of Patients With Relapsed or Refractory Indolent Non-Hodgkin's Lymphoma (NHL)

Study ID: NCT00060671

Study Description

Brief Summary: The purpose of this study is to determine whether combining pixantrone (BBR 2778, INN name pending) with the monoclonal antibody rituximab, leads to an increase in the period of patients' remission, compared to rituximab alone.

Detailed Description: This trial is being conducted in patients with indolent (or low-grade) non-Hodgkin's lymphoma, who have either relapsed or been refractory to previous treatment. Pixantrone belongs to the DNA intercalator family of chemotherapy agents, which includes anthracyclines. DNA intercalators are commonly used to treat patients with indolent NHL, often in combination with the monoclonal antibody rituximab. This study represents the first large-scale, comparative trial in indolent NHL, designed to determine whether the response rate and time to tumour progression in patients treated with a combination of rituximab and a DNA intercalator, is significantly higher than seen in patients treated with rituximab alone. This trial is randomized and controlled, which means that participating patients will be randomly assigned to one of two treatment groups: 1. Patients treated with both pixantrone and rituximab, in combination 2. Patients treated with only rituximab This trial is expected to recruit around 800 patients in the US, Europe and Israel, with 400 patients recruited to each group. Patients will be treated for around 18 weeks and will recieve regular physician monitoring for five years from the end of treatment.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Arizona Clinical Research Center, Tucson, Arizona, United States

Sutter Health Western Division Cancer Research Group, Greenbrae, California, United States

Kenmar Research Institute, Los Angeles, California, United States

Rocky Moutain Cancer Center, Denver, Colorado, United States

Pasco, Hernando Oncology Associates, P.A., New Port Richey, Florida, United States

Ocala Oncology Center, Ocala, Florida, United States

Orange Park Cancer Center, Orange Park, Florida, United States

University of Chicago Medical Center Hematology / Oncology, Chicago, Illinois, United States

Illinois Masonic Cancer Center, Chicago, Illinois, United States

Edward Cancer Center, Naperville, Illinois, United States

Hope Center, Terre Haute, Indiana, United States

Commonwealth Hematology/Oncology, Danville, Kentucky, United States

New England Hematology / Oncology Associates, Wellesley, Massachusetts, United States

St. Joseph Oncology, St Joseph, Missouri, United States

Christian Hospital, St Louis, Missouri, United States

St. Johns Mercy Medical Center, St. Louis, Missouri, United States

Hematology - Oncology Centers of N. Rockies, Billings, Montana, United States

Great Falls Clinic, Great Falls, Montana, United States

East Orange VA Medical Center, East Orange, New Jersey, United States

Hematology Oncology Associates of NJ, Paramus, New Jersey, United States

Summit Medical Group/Overlook Onc Center, Summit, New Jersey, United States

New Mexico Oncology / Hematology, Albuquerque, New Mexico, United States

HemOnCare, P.C., Brooklyn, New York, United States

Glens Falls Cancer Center, Glens Falls, New York, United States

North Shore - Long Island Jewish Health System, New Hyde Park, New York, United States

New York University, New York, New York, United States

Upstate NY Cancer Research, Rochester, New York, United States

South Shore Hematology-Oncology Associates, Rockville Centre, New York, United States

Clinworks, Inc, Charlotte, North Carolina, United States

Private Practice, Canton, Ohio, United States

Blair Medical Associates, Altoona, Pennsylvania, United States

Lancaster Cancer Center, LTD, Lancaster, Pennsylvania, United States

Santee Hematology Oncology, Sumter, South Carolina, United States

The West Clinic, Memphis, Tennessee, United States

Central Utah Medical Clinic Hematology-Oncology, Provo, Utah, United States

Oncology of Wisconsin, Glendale, Wisconsin, United States

Marshfield Clinic, Marshfield, Wisconsin, United States

Rhinelander Regional Medical Group Onc., Rhinelander, Wisconsin, United States

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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