US2023114726A1PendingUtilityA1

Methods and compositions for treatment of amyloid deposition diseases

Assignee: UNIV COLUMBIAPriority: Aug 1, 2017Filed: Jul 12, 2022Published: Apr 13, 2023
Est. expiryAug 1, 2037(~11 yrs left)· nominal 20-yr term from priority
A61K 2039/545A61K 39/39541A61K 39/3955A61K 2039/55A61K 2039/57A61P 43/00A61K 2039/58C07K 16/18C07K 2317/24A61K 2039/505A61P 25/28A61K 49/16
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Claims

Abstract

Methods and pharmaceutical compositions for treatment of amyloid deposition diseases using chimeric (e.g., mouse-human) antibody are disclosed, including a method for treating amyloid deposition diseases with cardiac involvement by administering pharmaceutical compositions comprising a chimeric anti-amyloid fibril antibody. The methods herein can improve myocardial function in patients diagnosed with light chain amyloid light chain amyloidosis (ALA) having a cardiac involvement in as little as three weeks after treatment.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of detecting the presence of amyloid deposits in a patient suspected of having such deposits which comprises administering to the patient an amount of a chimeric mouse-human antibody which comprises a V κ  region comprising SEQ ID NO: 47 and a V H  region comprising SEQ ID NO: 48 and having a detectable label attached thereto, the amount of antibody administered being sufficient to allow detection of amyloid deposits if such are present. 
     
     
         2 . The method of  claim 1 , wherein the detectable label is  124 I. 
     
     
         3 . A method of monitoring improvement in myocardial function in a patient diagnosed with light chain amyloidosis (ALA) with cardiac involvement comprising observing an improvement in myocardial function in a patient diagnosed with ALA having a cardiac involvement within about three weeks after administration to said patient of a therapeutically effective amount of a humanized or chimeric 11-1F4 antibody or an antigen-binding fragment thereof. 
     
     
         4 . The method of  claim 3 , wherein the patient suffers from relapse or refractory ALA. 
     
     
         5 . The method of  claim 3 , wherein the ALA is further characterized as having light chain lambda amyloid cardiac involvement. 
     
     
         6 . The method of  claim 3 , wherein the ALA is further characterized as having light chain kappa amyloid cardiac involvement.

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