US2019314342A1PendingUtilityA1

Method for treating demyelinating neuropathy with biotin

Assignee: MEDDAY PHARMACEUTICALSPriority: Mar 26, 2015Filed: Jun 25, 2019Published: Oct 17, 2019
Est. expiryMar 26, 2035(~8.7 yrs left)· nominal 20-yr term from priority
A61K 31/4188A61K 9/0019A61P 25/28A61K 45/06A61P 21/00A61K 9/0053A61P 25/00
58
PatentIndex Score
0
Cited by
0
References
0
Claims

Abstract

The invention relates to the use of biotin for treating Amyotrophic Lateral Sclerosis, as well as demyelinating peripheral neuropathies and Neuromyelitis optica (NMO).

Claims

exact text as granted — not AI-modified
1 - 20 . (canceled) 
     
     
         21 . A method for the treatment of a demyelinating neuropathy, comprising administering to a patient in need thereof a composition comprising an amount of biotin sufficient to treat said demyelinating neuropathy. 
     
     
         22 . The method of  claim 21 , wherein the demyelinating neuropathy is a peripheral demyelinating neuropathy. 
     
     
         23 . The method of  claim 21 , wherein the demyelinating neuropathy is a demyelinating neuropathy associated with immunoglobulin M (lgM) monoclonal gammopathy and antibodies against myelin-associated glycoprotein (MAG), typical chronic inflammatory demyelinating polyradiculoneuropathy, atypical chronic inflammatory demyelinating polyradiculoneuropathy, Charcot Marie Tooth la disease and Guillain-Barre syndrome. 
     
     
         24 . The method of  claim 21 , wherein the demyelinating neuropathy is neuromyelitis optica. 
     
     
         25 . The method of  claim 21 , wherein the demyelinating neuropathy is amyotrophic lateral sclerosis. 
     
     
         26 . The method of  claim 21 , wherein a daily amount of biotin administered to the patient is between 50 and 700 mg. 
     
     
         27 . The method of  claim 21 , wherein a daily amount of biotin administered to the patient is at least 100 mg. 
     
     
         28 . The method of  claim 21 , wherein a daily amount of biotin administered to the patient is at least 150 mg. 
     
     
         29 . The method of  claim 21 , wherein a daily amount of biotin administered to the patient is between 100 and 300 mg. 
     
     
         30 . The method of  claim 21 , wherein the composition is in a form suitable for oral administration. 
     
     
         31 . The method of  claim 21 , wherein the composition is in the form of gel capsules, tablets (optionally film-coated), lozenges or pills. 
     
     
         32 . The method of  claim 21 , wherein the composition comprises excipients and biotin as the sole active ingredient. 
     
     
         33 . The method of  claim 21 , wherein the composition is in a form suitable for injectable administration. 
     
     
         34 . The method of  claim 21 , wherein the composition is in a form of a slow release composition. 
     
     
         34 . The method of  claim 21 , wherein the treatment with biotin has a duration of at least 3 months. 
     
     
         35 . The method of  claim 21 , wherein the treatment with biotin has a duration of at least 6 months. 
     
     
         36 . The method of  claim 21 , wherein the treatment with biotin has a duration of at least one year. 
     
     
         37 . The method of  claim 21 , wherein the treatment includes simultaneous, separate or sequential administration of one or more active ingredients in addition to biotin. 
     
     
         38 . The method of  claim 37 , wherein the one or more active ingredients riluzole, baclofen, diazepam trihexyphenidyl, amitriptyline, corticosteroids, plasmapheresis azathioprine, mycophenolate mofetil, rituximab, mitoxantrone, glatiramer acetate, intravenous immunoglobulin (IVIG), and/or cyclophosphamide. 
     
     
         39 . A composition comprising an amount of biotin sufficient to treat a demyelinating neuropathy.

Join the waitlist — get patent alerts

Track US2019314342A1 — get alerts on status changes and closely related new filings.

We store only your email — no account needed. See our privacy policy.