US2017056482A1PendingUtilityA1

Method for treating systemic dna mutation disease

Assignee: CLS THERAPEUTICS LTDPriority: Jul 14, 2003Filed: Oct 6, 2016Published: Mar 2, 2017
Est. expiryJul 14, 2023(expired)· nominal 20-yr term from priority
C12Q 1/6883C12Y 301/00C12Y 301/21001A61K 38/465C12Q 2600/156
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Claims

Abstract

The invention is directed to treatment of systemic DNA mutation diseases accompanied with development of somatic mosaicism and elevation of blood extracellular DNA. The inventive method comprises introducing a DNASE enzyme into the systemic blood circulation of a patient in doses and regimens which are sufficient to decrease average molecular weight of circulating extracellular blood DNA in the blood of said patient.

Claims

exact text as granted — not AI-modified
1 . A method for suppressing spread of mutated DNA sequences within the body and development of somatic mosaicism in a subject in need thereof, wherein said method comprises administering a DNase enzyme to said subject, wherein said DNase enzyme is administered in a dose and regimen which is sufficient to decrease the average molecular weight of extracellular blood DNA in the blood of said subject. 
     
     
         2 - 4 . (canceled) 
     
     
         5 . The method according to  claim 1 , wherein said DNase enzyme is administered in a dose and regimen that results in a DNA hydrolytic activity measured in blood plasma that exceeds 1.5 Kunitz units per 1 ml of blood plasma for more than 12 hours within a period of 24 hours. 
     
     
         6 . The method of  claim 1 , wherein the subject has a cancer and the development of somatic mosaicism results from a spread of mutated DNA sequences promoting cancer development. 
     
     
         7 . The method of  claim 6 , wherein the subject has a metastatic cancer and the development of somatic mosaicism results from a spread of mutated DNA sequences promoting metastasis development. 
     
     
         8 . The method of  claim 1 , wherein the subject has a cancer and is receiving a chemotherapy and the development of somatic mosaicism results from a spread of mutated DNA sequences promoting resistance to said cancer chemotherapy.

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