US2014121157A1PendingUtilityA1
Methods for treating progressive cognitive disorders related to neurofibrillary tangles
Est. expirySep 7, 2025(expired)· nominal 20-yr term from priority
A61K 38/33A61P 25/00A61K 45/06A61K 38/28A61P 25/28A61K 38/22A61K 38/2264A61K 38/17A61K 38/16
57
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Claims
Abstract
The described invention provides methods for treating or preventing progression of a progressive cognitive disease, disorder or condition, and methods for improving resilience of cognitive function in a subject in need thereof.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method for treating a progressive cognitive disorder, the method comprising the step of:
(a) administering to a subject in need thereof a first composition comprising
(i) a phosphorylated tau accumulation-modulating amount of a leptin composition, or a pharmaceutically acceptable salt thereof, and
(ii) a pharmaceutically acceptable carrier, and
(b) modulating accumulation of phosphorylated tau in cerebrospinal fluid of the subject.
2 . The method according to claim 1 , wherein the progressive cognitive disorder is selected from the group consisting of progressive supranuclear palsy, dementia, dementia pugilistica, Creutzfeldt-Jakob disease, frontotemporal dementia, Pick's disease, and FTDP-17 (parkinsonism) corticobasal degeneration.
3 . The method according to claim 1 , wherein the leptin composition is a leptin, or a pharmaceutically acceptable salt thereof.
4 . The method according to claim 1 , wherein the leptin composition is a leptin mimic, or a pharmaceutically acceptable salt thereof.
5 . The method according to claim 1 , wherein the leptin composition is a leptin derivative, or a pharmaceutically acceptable salt thereof.
6 . The method according to claim 1 , wherein the leptin composition is a leptin agonist, or a pharmaceutically acceptable salt thereof.
7 . The method according to claim 1 , wherein the phosphorylated tau accumulation modulating amount is an amount from about 0.01 mg/kg body weight to about 100 mg/kg body weight.
8 . The method according to claim 1 , wherein the first composition further comprises a second therapeutic agent.
9 . The method according to claim 8 , wherein the second therapeutic agent is at least one of an antibiotic, an anti-fungal agent, an antiviral agent, an anti-protozoal agent, a steroidal anti-inflammatory agent, a non-steroidal anti-inflammatory agent, an anti-oxidant; a hormone; a vitamin; an antihistamine agent. and a chemotherapeutic agent.
10 . The method according to claim 1 , wherein the progressive disorder comprises accumulation of neurofibrillary tangles in brain.
11 . A method for improving resilience of cognitive function in a subject in need thereof, the method comprising the step of
(a) administering to the subject a composition comprising:
i. a cognitive function-enhancing amount of a leptin composition, and
ii. a pharmaceutically acceptable carrier; and
(b) modulating accumulation of phosphorylated tau in cerebrospinal fluid of the subject.
12 . The method according to claim 11 , wherein the leptin composition comprises at least one of a leptin, a leptin mimic, a leptin derivative, an AMP-dependent protein kinase activator, a leptin agonist, a leptin blocker, a mimic of a leptin blocker, a leptin antagonist, an AMP-dependent protein kinase inhibitor; or pharmaceutically acceptable salts thereof.
13 . The method according to claim 11 , wherein the leptin composition further comprises a second therapeutic agent.
14 . The method according to claim 13 , wherein the second therapeutic agent is at least one of an antibiotic, an anti-fungal agent, an antiviral agent, an anti-protozoal agent, a steroidal anti-inflammatory agent, a non-steroidal anti-inflammatory agent, an anti-oxidant; a hormone; a vitamin; an antihistamine agent. and a chemotherapeutic agent.Cited by (0)
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