US2019153052A1PendingUtilityA1

Treatment with a pharmaceutical composition comprising manf2 nucleic acid

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Assignee: HERANTIS PHARMA PLCPriority: Aug 30, 2002Filed: Oct 17, 2014Published: May 23, 2019
Est. expiryAug 30, 2022(expired)· nominal 20-yr term from priority
A61P 25/00A61P 25/08A61P 25/16A61P 25/30A61P 25/02A61P 25/28A01K 2217/075C07K 14/475A01K 2217/05A01K 2227/105A01K 2267/0356A61K 38/00
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Claims

Abstract

A method for treating a condition in a patient, wherein the condition is selected from the group consisting of Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, stroke and peripheral neuropathy. The method consists of administering to the patient a pharmaceutically effective amount of a pharmaceutical composition comprising the MANF2 polypeptide of SEQ ID NO:2 or a functional fragment thereof.

Claims

exact text as granted — not AI-modified
What is claimed: 
     
         1 . A method of treating the symptoms of amyotrophic lateral sclerosis, ALS, in a patent in need thereof, the method comprising:
 directly administering to the central nervous system of the patient a pharmaceutically effective amount of a pharmaceutical composition comprising the MANF2 polypeptide of SEQ ID NO:2 or a functional fragment thereof, wherein said functional fragment is capable of preventing the 6-hydroxydopamine (6-OHDA)-induced degeneration of dopaminergic neurons, and wherein said functional fragment comprises amino acids 27-187 of the amino acid sequence SEQ ID NO:2.   
     
     
         2 . The method of  claim 1 , wherein the pharmaceutical composition comprises SEQ ID NO:2. 
     
     
         3 . The method of  claim 1 , wherein the functional fragment consists of amino acids 27-187 of the amino acid sequence of SEQ ID NO:2.

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