US2019314342A1PendingUtilityA1
Method for treating demyelinating neuropathy with biotin
Est. expiryMar 26, 2035(~8.7 yrs left)· nominal 20-yr term from priority
Inventors:Frédéric Sedel
A61K 31/4188A61K 9/0019A61P 25/28A61K 45/06A61P 21/00A61K 9/0053A61P 25/00
58
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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-modified1 - 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
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