US2020360393A1PendingUtilityA1
Use of (2r, 6r)-hydroxynorketamine, (s)-dehydronorketamine and other stereoisomeric dehydro and hydroxylated metabolites of (r,s)-ketamine in the treatment of depression and neuropathic pain
Assignee: THE US SECRETARY DEPARTMENT OF HEALTH AND HUMAN SERVICPriority: Oct 14, 2011Filed: Jul 31, 2020Published: Nov 19, 2020
Est. expiryOct 14, 2031(~5.2 yrs left)· nominal 20-yr term from priority
Inventors:Irving W. WainerRuin MoaddelMichel BernierCarlos ZarateMarc C. TorjmanMichael E. GoldbergMary J. Tanga
A61K 45/06A61K 31/135C07D 295/15A61P 25/18C07C 2601/16A61P 25/28C07D 295/108A61K 31/165A61K 31/5375A61P 25/00A61K 31/265A61K 31/137C07C 225/20C07C 237/04A61K 31/4453C07C 2601/14A61K 31/222C07B 2200/07A61P 21/02C07D 295/155C07D 295/112A61P 25/24A61P 25/04C07C 237/20C07C 229/48A61P 29/00A61K 31/24
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Claims
Abstract
The disclosure also provides novel ketamine metabolite prodrugs. The disclosure provides methods of treating, bipolar depression, major depressive disorder, neuropathic and chronic pain, including complex regional pain synthetic pain disorder (CRPD) by administering a purified ketamine metabolite or a ketamine metabolite prodrug directly to patients in need of such treatment.
Claims
exact text as granted — not AI-modified1 - 36 . (canceled)
37 . A pharmaceutical composition comprising a compound or a pharmaceutically acceptable salt thereof, wherein the compound is
together with a pharmaceutically acceptable excipient; wherein
(a) the composition is a solution and contains from about 0.05 mg/ml to about 0.5 mg/ml of the compound;
(b) the composition is an intravenous composition that provides about 0.2 mg to about 500 mg per administration; or
(c) the composition is formulated for oral administration and contains about 0.2 mg to about 500 mg of the compound.
38 . A pharmaceutical composition comprising a compound or pharmaceutically acceptable salt thereof, where the compound is a compound of the formula
together with a pharmaceutically acceptable excipient; wherein
(a) the composition is a solution and contains from about 0.05 mg/ml to about 0.5 mg/ml of the compound;
(b) the composition is an intravenous composition that provides about 0.2 mg to about 500 mg per administration; or
(c) the composition is formulated for oral administration and contains about 0.2 mg to about 500 mg of the compound.
39 . An intravenous pharmaceutical composition comprising a compound or pharmaceutically acceptable salt thereof, where the compound is a compound of the formula
and the intravenous pharmaceutical composition provides a plasma Cmax of about 0.25 mcg/mL to about 125 mcg/mL
40 . The intravenous pharmaceutical composition of claim 39 , wherein the composition provides a plasma Cmax of about 1 mcg/mL to about 50 mcg/mL
41 . The pharmaceutical composition of claim 1 , wherein the compound is 2R,6R-hydroxynoreketamine.
42 . The pharmaceutical composition of claim 38 , wherein the composition is a solution and contains from about 0.05 mg/ml to about 0.5 mg/ml of the compound or salt thereof.
43 . The pharmaceutical composition of claim 38 , wherein the composition is an intravenous composition that provides about 0.2 mg to about 500 mg of the compound per administration.
44 . The pharmaceutical composition of claim 38 , wherein the composition is formulated for oral administration and contains about 0.2 mg to about 500 mg of the compound or salt thereof.
45 . The pharmaceutical composition of claim 38 , wherein the composition is formulated for oral administration and contains about 10 mg to about 200 mg of the compound or salt thereof.
46 . A method of treating bipolar depression, major depressive disorder, schizophrenia, Alzheimer's dementia, amyotrophic lateral sclerosis, complex regional pain syndrome (CRPS), chronic pain, or neuropathic pain in a patient comprising administering an effective amount of a pharmaceutical composition of claim 37 to the patient.
47 . A method of treating bipolar depression, major depressive disorder, schizophrenia, Alzheimer's dementia, amyotrophic lateral sclerosis, complex regional pain syndrome (CRPS), chronic pain, or neuropathic pain in a patient comprising administering an effective amount of a pharmaceutical composition of claim 38 to the patient.
48 . A method of treating a patient for bipolar depression, major depressive disorder, schizophrenia, Alzheimer's dementia, amyotrophic lateral sclerosis, complex regional pain syndrome (CRPS), chronic pain, or neuropathic pain comprising
(1) determining that the patient is a ketamine non-responder; and (2) administering an effective amount of a pharmaceutical composition of claim 38 to the patient.Join the waitlist — get patent alerts
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