A Phase 1 interventional study of Chimeric anti-CD20 monoclonal antibody in B-cell Non Hodgkin's Lymphoma, sponsored by Sinocelltech Ltd.. Completed. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2014-08-01.
Sponsored by Sinocelltech Ltd. · Phase 1, Interventional, and Treatment
The purpose of this study is to determine whether SCT400 is safe and effective in the treatment of B-cell Non Hodgkin's lymphoma
5,578 studies on the registry are indexed under Lymphoma; 825 are open to participants now.
This study's enrollment of 15 is below the median of 40 across 4,508 interventional studies indexed under Lymphoma.
Browse Lymphoma studies →Sinocelltech Ltd. is the lead sponsor of 78 studies on the registry; 32 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Three escalating single-dose groups of chimeric anti-CD20 monoclonal antibody(SCT400) : 250 mg/m2 , 375 mg/m2,500 mg/m2, once a week for 4 doses;
Biological: Chimeric anti-CD20 monoclonal antibody
Also known as: SCT400
Number of participants with infusion-related reaction and with drug-related adverse events.
Time frame: up to 27 weeks
Area Under the plasma concentration versus time curve (AUC) of SCT400
Time frame: prior to the initial dose on day 1 and 0,2,4,8,24,48,72,96,120 hours post-dose
Time to disease progression
Time frame: up to 27 weeks
No study locations are listed for this record.
This study is completed, as verified in Dec 2013. You cannot join it, but the record below documents what was studied.
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Sinocelltech Ltd.