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Monoclonal Antibody Therapy for Non-Hodgkin's Lymphoma
Study Summary
This trial will compare two different monoclonal antibody regimens to see which is more effective in treating patients with relapsed or refractory non-Hodgkin's lymphoma.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Treatment Details
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Who is running the clinical trial?
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- I have never received Hu1D10 monoclonal antibody treatment.It has been over 3 months since my last radioimmunotherapy.My non-Hodgkin lymphoma has not improved or has worsened since my last treatment.My cancer can be measured and is at least 2 cm big in one direction.It has been over 3 months since my last immunotherapy treatment.I haven't taken high doses of steroids in the last 4 weeks.My lymphoma is 1D10+ as confirmed by specific tests.I am not receiving any other treatments for lymphoma.I haven't had any cancer except for skin cancer or early-stage cancer in the last 2 years.My cancer has not spread to my brain.I am able to get out of my bed or chair and move around.I do not have major psychiatric or brain function issues.It has been over 4 weeks since my last interferon therapy.I am not taking more than 10 mg of prednisone daily for any condition.I am 18 years old or older.My heart condition does not severely limit my daily activities.My neutrophil count is at least 1,000/mm^3.I haven't had a heart attack or untreated heart rhythm problems in the last 6 months.I do not have any serious lung problems.It has been over 4 weeks since my last external beam radiotherapy.It has been over 4 weeks since my last chemotherapy.My lymphoma has returned or didn't respond to treatment.I have had treatments like radiotherapy, immunotherapy, or chemotherapy for non-Hodgkin lymphoma.I do not have any serious infections.
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
What is the risk-benefit ratio of this medical treatment?
"With the available data, our team at Power evaluated this treatment's safety to be a 2. This assessment is based on the fact that it has only reached Phase 2 clinical trials, providing some evidence of its security but no proof of effectiveness."
Is this research actively looking for participants?
"Per the clinicaltrials.gov platform, this medical trial is not currently seeking out patients for participation. Initially posted on October 1st 2000 and last updated December 17th 2013, it does not require any new volunteers as of now. Fortunately, there are a plethora of similar trials recruiting participants at present; over 1750 in total."
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