US2016060331A1PendingUtilityA1

Prevention and treatment of synucleinopathic and amyloidogenic disease

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Assignee: PROTHENA BIOSCIENCES LTDPriority: Feb 23, 2007Filed: Aug 31, 2015Published: Mar 3, 2016
Est. expiryFeb 23, 2027(~0.6 yrs left)· nominal 20-yr term from priority
A61P 25/28A61P 25/16A61K 2039/575A61K 39/0007C07K 16/18A61K 2039/55566C07K 2317/21A61K 2039/505C07K 2317/34C07K 2317/92
56
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Claims

Abstract

The invention provides improved agents and methods for treatment of diseases associated with synucleinopathic diseases, including Lewy bodies of alpha-synuclein in the brain of a patient. Such methods entail administering agents that induce a beneficial immunogenic response against the Lewy body. The methods are particularly useful prophylactic and therapeutic treatment of Parkinson's disease.

Claims

exact text as granted — not AI-modified
1 . A method of effecting prophylaxis or treating a disease characterized by Lewy bodies or alpha-synuclein aggregation in the brain, the method comprising administering to a patient having or at risk of the disease an effective regime of a monoclonal antibody that competes with mouse monoclonal antibody 9E4 (ATCC accession number PTA-8221) for binding to human alpha-synuclein having the sequence according to SEQ ID NO:1. 
     
     
         2 . (canceled) 
     
     
         3 . The method of  claim 1 , wherein the disease is Parkinson's disease. 
     
     
         4 . (canceled) 
     
     
         5 . The method of  claim 1 , wherein the antibody is a chimeric antibody, a human antibody, or a humanized antibody. 
     
     
         6 - 7 . (canceled) 
     
     
         8 . The method of  claim 1 , wherein the antibody is an antibody of human IgG1 isotype. 
     
     
         9 . The method of  claim 1 , wherein the antibody is administered with a pharmaceutical carrier as a pharmaceutical composition. 
     
     
         10 . The method of  claim 9 , wherein the antibody is administered at a dosage of 0.0001 to 100 mg antibody/kg body weight. 
     
     
         11 . The method of  claim 9 , wherein the antibody is administered in multiple dosages over at least six months. 
     
     
         12 . The method of  claim 9 , wherein the antibody is administered intraperitoneally, orally, subcutaneously, intracranially, intramuscularly, topically, intranasally or intravenously. 
     
     
         13 . The method of  claim 9 , wherein the antibody is administered by a peripheral route. 
     
     
         14 . The method of  claim 9 , wherein the antibody is administered at a dose of 1-10 mg/kg. 
     
     
         15 - 32 . (canceled)

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