US2007148714A1PendingUtilityA1

Clinical Parameters for Determining Hematologic Toxicity Prior to Radioimmunotherapy

Assignee: RAESTETTER WILLIAMPriority: Aug 11, 1999Filed: Feb 27, 2007Published: Jun 28, 2007
Est. expiryAug 11, 2019(expired)· nominal 20-yr term from priority
A61P 35/00A61K 51/1027C07K 16/2896G01N 33/5094C07K 16/2887G01N 33/5091A61K 2039/505
52
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Claims

Abstract

New clinical parameters are reported which may serve as predictors of the hematological toxicity associated with therapeutic radiolabeled antibodies, particularly those antibodies which target lymphoma cells which have a tendency to localize to the bone marrow.

Claims

exact text as granted — not AI-modified
1 . A method of predicting the severity of hematologic toxicity which would result from administration of a radiolabled antibody to a cancer patient deterring or decreasing such hematological toxicity, comprising: 
 (a) measuring the degree of bone marrow involvement in a baseline biopsy; and    (b) administering a therapeutically effective amount of non-labeled, depleting antibody if said baseline bone marrow involvement is higher than 5% such that said bone marrow involvement is decreased to less than 5%.    
   
   
       2 - 52 . (canceled)

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