US2003099636A1PendingUtilityA1

Curing method for pathologic syndrome and medicinal preparation

Priority: Jun 20, 2000Filed: Jun 19, 2001Published: May 29, 2003
Est. expiryJun 20, 2020(expired)· nominal 20-yr term from priority
A61P 3/04A61P 9/00A61P 9/10A61P 37/00A61P 43/00C07K 2317/77A61P 31/00C07K 16/26C07K 16/245A61K 2039/545A61P 29/00A61K 31/277C07K 16/00C07K 16/249C07K 16/28A61P 25/30A61K 41/0004A61P 25/18A61P 31/12C07K 16/44C07K 2317/73C07K 16/243C07K 16/22A61K 2039/505C07K 16/24A61P 25/34A61P 25/28C07K 16/2806C07K 16/248C07K 16/40A61P 25/36A61P 25/24A61P 25/32A61P 25/16A61K 39/39583C07K 16/241C07K 16/246A61P 3/10C07K 2317/75
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Claims

Abstract

A method of treating a pathological syndrome includes administration of an activated form of ultra-low doses of antibodies to an antigen, wherein said activated form is obtained by repeated consecutive dilution combined with external impact, and the antigen is a substance or a pharmaceutical agent exerting influence upon the mechanisms of formation of this particular pathological syndrome. Pharmaceutical agent for treating a pathological syndrome contains activated form of ultra-low doses of monoclonal, polyclonal or natural antibodies to an antigen, wherein said activated form is prepared by means of repeated consecutive dilution and external treatment, predominantly based on homeopathic technology, and said antigen is a substance or a drug acting as a direct cause of the pathological syndrome or involved in regulation of mechanisms of its formation. At that, activated forms of ultra-low doses of antibodies are raised against antigens of exogenous or endogenous origin, against autologous antigens, fetal antigens; anti-idiotypic antibodies are used too.

Claims

exact text as granted — not AI-modified
1 . A method of treating a pathological syndrome by administration of activated forms of ultra-low doses of antibodies to an antigen, wherein said activated forms are obtained by repeated consecutive dilution combined with external treatment, and said antigen is a substance or a pharmaceutical agent exerting influence upon the mechanisms of formation of the pathological syndrome.  
     
     
         2 . The method of treating a pathological syndrome described in  claim 1 , wherein said activated form of ultra-low doses of antibodies are produced by homeopathic technology.  
     
     
         3 . The method of treating a pathological syndrome described in  claim 1 , wherein said activated forms of ultra-low doses of antibodies to an antigen or hapten are administered together with this antigen, and said antigen or hapten is a substance or a pharmaceutical agent exerting influence upon the mechanisms of formation of the pathological syndrome.  
     
     
         4 . A method of treating a pathological syndrome by administration of activated forms of ultra-low doses of antibodies to an antigen, wherein said pathological syndrome is caused by introduction of the antigen, said activated forms are obtained by repeated consecutive dilution combined with external treatment, and said antigen is a substance or a pharmaceutical agent capable of causing intoxication and/or addiction.  
     
     
         5 . The method of treating a pathological syndrome described in  claim 4 , wherein said activated form of ultra-low doses of antibodies are produced by homeopathic technology.  
     
     
         6 . The method of treating a pathological syndrome described in  claim 4 , wherein said activated forms of ultra-low doses of antibodies to an antigen or hapten are administered together with this antigen, and said antigen or hapten is a substance or a pharmaceutical agent exerting influence upon the mechanisms of formation of the pathological syndrome.  
     
     
         7 . A method of treating a pathological syndrome by administration of activated forms of ultra-low doses of antibodies to an antigen, wherein said activated forms are obtained by repeated consecutive dilution combined with external treatment, and said antigen is a hapten conjugated with high-molecular compound, wherein said hapten is substance or a pharmaceutical agent exerting influence upon the mechanisms of formation of the pathological syndrome.  
     
     
         8 . The method of treating a pathological syndrome described in  claim 7 , wherein said activated forms of ultra-low doses of antibodies are produced by homeopathic technology.  
     
     
         9 . The method of treating a pathological syndrome described in  claim 7 , wherein said activated forms of ultra-low doses of antibodies to an antigen or hapten are administered together with this antigen, and said antigen or hapten is a substance or a pharmaceutical agent exerting influence upon the mechanisms of formation of the pathological syndrome.  
     
     
         10 . A method of treating a pathological syndrome by administration of activated forms of ultra-low doses of antibodies to an antigen, wherein said activated forms are obtained by repeated consecutive dilution combined with external treatment, said antigen is an antigen of a tissue or a tissue culture, and said antigen exerts influence upon the mechanisms of formation of pathological syndrome predominantly in this particular tissue.  
     
     
         11 . The method of treating a pathological syndrome described in  claim 10 , wherein said activated form of ultra-low doses of antibodies are produced by homeopathic technology.  
     
     
         12 . A pharmaceutical agent for treating a pathological syndrome containing an activated form of ultra-low doses of monoclonal, polyclonal or natural antibodies, wherein said activated form is produced by repeated consecutive dilution and external treatment predominantly based on homeopathic technology, and said antigen is a substance or a drug exerting influence upon the mechanisms of formation of the pathological syndrome.  
     
     
         13 . The pharmaceutical agent described in  claim 12 , wherein antibodies are raised to substances of exogenous origin.  
     
     
         14 . The pharmaceutical agent described in  claim 12 , wherein antibodies are raised to substances of endogenous origin.  
     
     
         15 . The pharmaceutical agent described in  claim 12 , wherein antibodies are raised to antigens of fetal tissues or tissue cultures.  
     
     
         16 . The pharmaceutical agent described in  claim 12 , wherein antibodies used are antiidiotypic antibodies.

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