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Monoclonal Antibodies

Iodine-131 Anti-B1 Antibody for Non-Hodgkin's Lymphoma

Phase 1
Waitlist Available
Research Sponsored by Corixa Corporation
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Patients must have a histologically confirmed initial diagnosis of low-grade non-Hodgkin's B-cell lymphoma according to International Working Formulation or de novo follicular large cell lymphoma
Patients must have been previously treated with chemotherapy and progressed on, failed to achieve an objective response on, or progressed after completion of their last chemotherapy
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights

Study Summary

This trial is testing a new cancer treatment that uses Iodine-131 Anti-B1 Antibody to target and kill cancer cells. The study will help doctors determine the best dose of the treatment and if it is safe and effective for patients with NHL who have cancer in their bone marrow.

Who is the study for?
This trial is for patients with stage IV non-Hodgkin's lymphoma (NHL) and significant bone marrow involvement. They must have previously undergone chemotherapy, have measurable disease, adequate organ function, and a life expectancy of at least 3 months. Excluded are those with HIV, prior radioimmunotherapy, certain heart diseases or other serious illnesses, recent cancer treatments or immunosuppressants, pregnancy or breastfeeding without agreed contraception.Check my eligibility
What is being tested?
The study tests the appropriate dose and assesses the effectiveness and safety of Iodine-131 Anti-B1 Antibody in treating NHL patients who've had previous treatments but still show more than 25% bone marrow involvement by lymphoma.See study design
What are the potential side effects?
Potential side effects may include reactions related to radiation exposure such as nausea and fatigue; blood count changes leading to increased infection risk; possible kidney or liver function impairment; allergic responses to antibody treatment.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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My initial diagnosis was low-grade non-Hodgkin's B-cell lymphoma or de novo follicular large cell lymphoma.
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My cancer did not respond or got worse after my last chemotherapy.
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My lymphoma is advanced (stage IV) with significant bone marrow involvement.
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I can care for myself and expect to live at least 3 more months.
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My tumor tests positive for the CD20 protein.
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I have a tumor that is at least 2 x 2 cm large.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 5 years for reporting.

Treatment Details

Find a Location

Who is running the clinical trial?

Corixa CorporationLead Sponsor
9 Previous Clinical Trials
566 Total Patients Enrolled
GlaxoSmithKlineIndustry Sponsor
4,750 Previous Clinical Trials
8,067,428 Total Patients Enrolled

Media Library

Iodine-131 Anti-B1 Antibody (Monoclonal Antibodies) Clinical Trial Eligibility Overview. Trial Name: NCT00022906 — Phase 1
Non-Hodgkin's Lymphoma Research Study Groups:
Non-Hodgkin's Lymphoma Clinical Trial 2023: Iodine-131 Anti-B1 Antibody Highlights & Side Effects. Trial Name: NCT00022906 — Phase 1
Iodine-131 Anti-B1 Antibody (Monoclonal Antibodies) 2023 Treatment Timeline for Medical Study. Trial Name: NCT00022906 — Phase 1

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is enrollment into this research endeavor still open?

"As per clinicaltrials.gov, this medical trial is not enrolling any more patients at present. The experiment was initially posted on May 1st 1999 and most recently edited on June 23rd 2005. Although recruitment for the study has ceased, there are 1779 other studies that still require participants to take part in them."

Answered by AI

To whom is enrollment in this clinical investigation available?

"This clinical trial is seeking 24 candidates who have been diagnosed with lymphoma and are aged 18 or older. In order to qualify, participants must possess a minimum performance status of 60% on the Karnofsky Performance Scale, an expected survival time frame of 3 months or greater, bi-dimensionally measurable disease (with at least one lesion being 2 x 2 cm in size), Ann Arbor Stage IV illness that has seen 25% or more involvement by NHL within the intratrabecular marrow space as observed via dual bone marrow biopsy specimens upon study entrance; alternatively a single biopsy can be done if it highlights over 50% involvement"

Answered by AI

Does this experiment accommodate participants older than 35 years?

"This medical study is enrolling participants aged 18 and older."

Answered by AI

What precautions should be taken in order to guarantee the security of those undergoing this therapy?

"Considering the lack of data on efficacy and safety, our assessment team at Power gave this treatment a score of 1."

Answered by AI
~1 spots leftby Apr 2025