A Phase 1/2 interventional study of IDEC-114 in Non-Hodgkin's Lymphoma, sponsored by Biogen. Completed at 4 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2012-06-08.
Sponsored by Biogen · Phase 1/2, Interventional, and Treatment
The purpose of this study is to determine whether anti-CD80 monoclonal antibody (IDEC-114) is effective in the treatment of follicular B-cell non-Hodgkin's lymphoma. This drug has never been studied in patients with lymphoma, however, it has been studied in psoriasis patients at various dose levels and schedules.
5,578 studies on the registry are indexed under Lymphoma; 825 are open to participants now.
This study's enrollment of 42 is close to the median of 40 across 4,508 interventional studies indexed under Lymphoma.
Browse Lymphoma studies →Biogen is the lead sponsor of 494 studies on the registry; 22 are open to participants now.
Of its 98 completed or terminated interventional studies of FDA-regulated products, 49 (50%) have results posted.
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Exclusion Criteria:
Drug: IDEC-114
Phase 1-A Group 1 - 125 mg/m2 x 4 infusions - Study Days 1, 8, 15, 22 Phase 1-A Group 2 - 250 mg/m2 x 4 infusions - Study Days 1, 8, 15, 22 Phase 1-A Group 3 - 375 mg/m2 x 4 infusions - Study Days 1, 8, 15, 22 Phase 1-B Group 4 - 500 mg/m2 x 4 infusions - Study Days 1, 8, 15, 22 Phase II-A \& II-B - Dosage start at the MTD (up to 375 mg/m2)
To characterize the safety profile of IDEC-114 and to define their duration and reversibility
Time frame: March 2010
To evaluate PK
Time frame: March 2010
To monitor presence of human anti galiximab antibody
Time frame: March 2010
To evaluate efficacy
Time frame: March 2010
To identify Nk functional assays that may predict galiximab efficacy
Time frame: March 2010
This study is completed, as verified in Jan 2011. You cannot join it, but the record below documents what was studied.
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