Safety and Efficacy of Zevalin in the Treatment of Non-Hodgkin's Lymphoma

Phase 3

Terminated

• Conditions: Non-Hodgkin's Lymphoma

• Registration Number: NCT00057343
• Lead Sponsor: Biogen

Brief Summary

The purpose of this study is to provide treatment for patients who have relapsed NHL or refractory NHL, and to determine the effectiveness and safety of the Zevalin and Rituxan regimens or Rituxan therapy alone on your disease.

Detailed Description

Not available

Study Timeline

• Study Start: 2003-03
• Study First Submitted: 2003-03-31
• Study First Submitted QC: 2003-03-31
• Study First Posted: 2003-04-01
• Status Verified: 2006-09
• Last Update Submitted: 2006-09-08
• Last Update Posted: 2006-09-12

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 400

Inclusion Criteria

• Histologically confirmed, relapsed or refractory CD20+ follicular B-cell NHL within 12 months of Study Day 1 (without clinical evidence of transformation). NHL must require treatment as determined by an increase in overall tumor size. The presence of B symptoms, and/or the presence of masses which are causing ongoing clinical symptoms.
• Bidimensionally measurable disease meeting the minimum requirement of at least 1 lesion >/= 2.0 cm in a single dimension.
• No lymphoma therapy for 3 weeks prior to Study Day 1.
• Patients must be recovered from all toxicities associated with prior surgery, radiation therapy, chemotherapy, or immunotherapy.
• Signed IRB-approved informed consent.
• Greater than 18 years of age.
• Expected survival >/= 3 months.
• WHO performance status of </= 2.
• Acceptable hematologic status, liver function, renal function, and pulmonary function.
• Female patients who are not pregnant or lactating.
• Men and women of reproductive potential who are following accepted birth control methods.

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Exclusion Criteria

• Patients with impaired bone marrow reserve, which may be indicated by prior myeloablative therapy with autologous bone marrow transplantation (ABMT) or peripheral blood stem cell (PBSC) rescue.
• Prior radioimmunotherapy, including the Zevalin regimen.
• Prior immunotherapy, including Rituxan therapy within 6 months of Study Day 1.
• Rituxan-refractory (no response to most recent Rituxan-containing regimen, or TTP was < 6 months).
• Presence of CNS lymphoma.
• Patients with chronic lymphocytic leukemia (CLL).
• Known history of HIV or AIDS.
• Serious nonmalignant disease or infection
• Major surgery, other than diagnostic surgery, within 4 weeks of Study Day 1.
• Patients who received investigational product within 4 weeks of Study Day 1 or patients who may experience long-term toxicity from a previous investigational therapy.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Event-free survival

Secondary Outcome Measures

Name	Time	Method
overall response rate
complete response rate
unconfirmed complete response rate
partial response rate
duration of response
time to progression
time-to-next anticancer therapy
quality of life
overall survival
safety profile

Trial Locations

Locations (2)

Research Site; 🇺🇸 Wausau, Wisconsin, United States

Biogen Idec Incorporated; 🇺🇸 San Diego, California, United States