Ketamine and Cannabis for the Treatment of Affective Disorders

Abstract

The invention features methods and compositions for treating an emotional disorder in a subject by administering ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof, and cannabis or a cannabinoid, in an amount sufficient to treat the emotional disorder.

Description

[Technical field]

[0001] The present invention relates to the field of methods for treating emotional disorders and other medical entities with symptoms related to emotional disorders or of a physical nature. Non-limiting examples of emotional disorders include anxiety, depression, somatization, and other categories of emotional disorders according to DSM-5-R. Anxiety disorders are the most commonly diagnosed mental illnesses in the United States. Non-limiting examples of anxiety disorders include generalized anxiety disorder (GAD), panic disorder (PD), social anxiety disorder (SAD), obsessive-compulsive disorder (OCD), specific phobia disorder (SPD), post-traumatic stress disorder (PTSD), agoraphobia, or separation anxiety disorder (SeAD). Non-limiting examples of depressive disorders include dysthymia, major depression, bipolar II disorder, postpartum depression, adjustment disorder with depression, and other depressive disorders. Non-limiting examples of physical symptoms that can be treated by the above methods include headaches, migraines, physical symptoms related to the menstrual cycle such as breast tenderness, abdominal pain, headaches, symptoms of somatization disorders, fibromyalgia, various neurological conditions and disorders, and pain from a wide variety of causes. [Background technology]

[0002] A significant portion of emotional disorders, including anxiety and depressive disorders, are refractory to currently used treatment methods. Summary of the Invention

[0003] The applicants have discovered that co-administration of ketamine and cannabis can be useful for treating emotional disorders. Long-term use of ketamine over decades has established its safety. In the methods described herein, the dosage is much lower than that used for anesthesia, and side effects are minimal. Cannabis is a medicinal plant that has been consumed by humans for thousands of years. Currently, the therapeutic benefits of cannabis are recognized by the majority of U.S. states and the District of Columbia where the medicinal use of cannabis has been legalized.

[0004] The invention features a method of treating an emotional disorder in a subject in need thereof, the method including administering to the subject (i) ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof, and (ii) cannabis or a cannabinoid, each in an amount sufficient together to treat the emotional disorder.

[0005] In a first embodiment of the above method, the emotional disorder is an anxiety disorder, which may be selected from or generalized to include generalized anxiety disorder (GAD), panic disorder (PD), social anxiety disorder (SAD), obsessive-compulsive disorder (OCD), specific phobia disorder (SPD), post-traumatic stress disorder (PTSD), agoraphobia, or separation anxiety disorder (SeAD).

[0006] In a second embodiment of the above method, the mood disorder is a depressive disorder. The depressive disorder may be selected from or generalized to include dysthymia, major depression, bipolar II disorder, postpartum depression, or adjustment disorder with depression.

[0007] In certain embodiments of the above methods, the present invention provides methods for treating a variety of physical symptoms that may or may not be associated with emotional disorders. Non-limiting examples of physical symptoms that may be treated by the above methods include headaches, migraines, physical symptoms related to the menstrual cycle, such as breast tenderness, abdominal pain, headaches, symptoms of somatization disorders, fibromyalgia, various neurological conditions and disorders, and pain from a wide variety of causes.

[0008] In some embodiments of the above method, the cannabis is a cannabis plant material, such as the buds or leaves of a plant of the species Cannabis indica, Cannabis sativa, Cannabis ruderalis, or a hybrid cannabis subspecies. In some embodiments, the cannabis plant material is smoked by the subject, for example with a cannabis-containing cigarette or from a pipe or other device. In some embodiments, the cannabis plant material is vaporized by the subject. In some embodiments, the cannabis is an extract, such as a concentrate or refined oil, of cannabis plant material containing at least one cannabinoid compound. In some embodiments, the oil and / or extract is vaporized by the subject. In some embodiments, the oil and / or concentrate is smoked by the subject. In some embodiments, the cannabis is formulated into a topical composition. In some embodiments, the cannabis is formulated into a tablet or capsule. In some embodiments, the cannabis is included in a foodstuff or beverage. In some embodiments, the cannabis is produced from a cannabis subspecies with high tetrahydrocannabinol (THC) content (e.g., containing at least 20% THC by dry weight, e.g., at least 20%, 21%, 22%, 23%, 24%, 25% or more THC). In some embodiments, the cannabis is a cannabis subspecies with high CBD content (e.g., containing at least 1% CBD by dry weight, e.g., at least 1%, at least 2%, 3%, 4%, 5% or more CBD). In some embodiments, the THC is (-)-trans-Δ 9 -Tetrahydrocannabinol (Delta-9-THC) or (-)-trans-Δ 8 -tetrahydrocannabinol (delta-8-THC). In some embodiments, the cannabinoid is (-)-trans-Δ 9 -Tetrahydrocannabivarin (Delta-9-THCV) or (-)-trans-Δ 8-tetrahydrocannabivarin (delta-8-THCV). In some embodiments, the cannabinoid is cannabinol. In some cases, the cannabinoid is cannabivarin (CBV).

[0009] In one embodiment of any of the above methods, the method can include initiating treatment after the subject's mood disorder appears.

[0010] In any of the above methods, ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof, and the cannabis product or cannabinoid are co-administered once or more per day, once or more every other day, or once or more every third day, or depending on the presence and / or severity of the affective disorder. For example, co-administration of ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof, and cannabis or cannabinoid can be once or twice per day for a period of 1 to 30 days, preferably with intervals of 10 days or less, and can then be repeated if clinically indicated (e.g., for 1 to 30 days, 2 to 29 days, 3 to 27 days, 4 to 26 days, 5 to 25 days, For a period of 6-24 days, 7-23 days, 8-22 days, 9-21 days, 10-20 days, 11-19 days, 12-18 days, 13-17 days, 14-16 days, or for 1 day, 2 days, 3 days, 4 days, 5 days, 6 days, 7 days, 8 days, 9 days, 10 days, 11 days, 12 days, 13 days, 14 days, 15 days, 16 days, 17 days, 18 days, 19 days, 20 days, or 21 days or for a period of 30 days or less, 29 days or less, 28 days or less, 27 days or less, 26 days or less, 25 days or less, 24 days or less, 23 days or less, 22 days or less, 21 days or less, 20 days or less, 19 days or less, 18 days or less, 17 days or less, 16 days or less, 15 days or less, 14 days or less, 13 days or less, 12 days or less, 11 days or less, 10 days or less, 9 days or less, 8 days or less, 7 days or less, 6 days or less, 5 days or less, 4 days or less, 3 days or less, or 2 days or less), followed by a period of at least 1 week or at least 2 weeks during which ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof, and cannabis or a cannabinoid are not co-administered to the subject. In certain embodiments, co-administration occurs once or more per day or intermittently over a period of 1 to 30 days, followed by variable periods during which ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof, and cannabis or a cannabinoid are not co-administered to the subject, which may be administered prior to sleep, but not during the sleep cycle.In such embodiments, they are not administered once a day for more than four weeks at a time, but generally less frequently and not consecutively on any particular day unless clinically supported for such use. In certain embodiments, ketamine, norketamine, 6-hydroxynorketamine, or a pharmaceutically acceptable salt thereof, and cannabis or cannabinoids are co-administered to a subject only in the evening. In certain embodiments, ketamine, norketamine, 6-hydroxynorketamine, or a pharmaceutically acceptable salt thereof, and cannabis or cannabinoids are co-administered to a subject one or more times a day in the evening. In certain embodiments, ketamine, norketamine, 6-hydroxynorketamine, or a pharmaceutically acceptable salt thereof, and cannabis or cannabinoids are co-administered to a subject one or more times during the day. In certain embodiments, ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof, and cannabis or a cannabinoid are co-administered to a subject one or more times daily and / or in the evening.

[0011] In certain embodiments of any of the above methods, the method includes administering to the subject an average daily dose of 1 mg to 500 mg (e.g., 10 mg to 200 mg, 25 mg to 150 mg, 35 mg to 125 mg, 50 mg to 250 mg, or 100 mg to 500 mg) of ketamine, or a pharma- ceutically acceptable salt thereof. For example, the method can include administering to the subject an average daily dose of 10 mg to 200 mg or 100 mg to 500 mg (e.g., 30±20 mg, 60±20 mg, 90±20 mg, 150±50 mg, 250±50 mg, 350±50 mg, or 450±50 mg) of enantiomerically pure S-(+)-ketamine, or a pharma- ceutically acceptable salt thereof. In certain embodiments, the methods include administering to the subject an average daily dose of 10 mg to 200 mg or 100 mg to 500 mg (e.g., 30±20 mg, 60±20 mg, 90±20 mg, 150±50 mg, 250±50 mg, 350±50 mg, or 450±50 mg) of enantiomerically pure R-(-)-ketamine, or a pharma- ceutically acceptable salt thereof. In some embodiments, the methods include administering to the subject an average daily dose of 10 mg to 200 mg or 100 mg to 500 mg (e.g., 30±20 mg, 60±20 mg, 90±20 mg, 150±50 mg, 250±50 mg, 350±50 mg, or 450±50 mg) of racemic ketamine, or a pharma- ceutically acceptable salt thereof.

[0012] In some embodiments of any of the above methods, the method includes administering to the subject one or more doses of 1 mg to 500 mg (e.g., 10 mg to 200 mg, 25 mg to 150 mg, 35 mg to 125 mg, 50 mg to 250 mg, or 100 mg to 500 mg) of norketamine, or a pharma- ceutically acceptable salt thereof. For example, the method can include administering to the subject an average daily dose of 10 mg to 200 mg (e.g., 30±20 mg, 60±20 mg, 90±20 mg, or 150±50 mg) of enantiomerically pure S-(+)-norketamine, or a pharma- ceutically acceptable salt thereof. In certain embodiments, the methods include administering to the subject an average daily dose of 10 mg to 200 mg (e.g., 30±20 mg, 60±20 mg, 90±20 mg, or 150±50 mg) of enantiomerically pure R-(-)-norketamine, or a pharma- ceutically acceptable salt thereof. In some embodiments, the methods include administering to the subject an average daily dose of 10 mg to 200 mg (e.g., 30±20 mg, 60±20 mg, 90±20 mg, or 150±50 mg) of racemic norketamine, or a pharma- ceutically acceptable salt thereof.

[0013] In some embodiments of any of the above methods, the method includes administering to the subject one or more doses of 1 mg to 500 mg (e.g., 10 mg to 200 mg, 25 mg to 150 mg, 35 mg to 125 mg, 50 mg to 250 mg, or 100 mg to 500 mg) of 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof. For example, the method can include administering to the subject an average daily dose of 10 mg to 200 mg (e.g., 30±20 mg, 60±20 mg, 90±20 mg, or 150±50 mg) of isomerically pure (2R,6R)-6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof. In certain embodiments, the methods include administering to the subject an average daily dose of 10 mg to 200 mg (e.g., 30±20 mg, 60±20 mg, 90±20 mg, or 150±50 mg) of isomerically pure (2S,6S)-6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof.

[0014] In certain embodiments of any of the above methods, administration of ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof is by a route selected from oral, sublingual, intranasal, intramuscular, intravenous, transdermal, intravaginal, and rectal administration, or any route of administration described herein.

[0015] In certain embodiments of the above methods, ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof is formulated into a lozenge.

[0016] In certain embodiments of any of the above methods, administration of cannabis or cannabinoid is by a route selected from oral, pulmonary or transdermal administration, or any route of administration described herein.

[0017] In certain embodiments of any of the above methods, ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof is administered in an amount or in a dosage form (e.g., a sustained release dosage form) that, when administered to a subject, does not result in anesthesia in the subject.

[0018] In certain embodiments of the above method embodiments, administration of ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof and cannabis or a cannabinoid improves the anesthetic effect of ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof, as compared to the anesthetic effect caused by administration of ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof alone. For example, a subject administered ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof alone may experience reduced sedation, observable as a lower score on a scale intended to measure sedation, such as the Richmond Agitation-Sedation Scale, as compared to a subject administered ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof in combination with cannabis.

[0019] In certain embodiments of the methods of the present invention, ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof, and cannabis or a cannabinoid are administered separately within 60 minutes, 30 minutes, or 15 minutes of each other.

[0020] In some embodiments, ketamine, norketamine, 6-hydroxynorketamine, or a pharmaceutically acceptable salt thereof, and cannabis or cannabinoids are co-administered. In certain embodiments, ketamine, norketamine, 6-hydroxynorketamine, or a pharmaceutically acceptable salt thereof, and cannabis or cannabinoids are formulated together and co-administered. In certain embodiments, the method includes (i) ketamine, norketamine, 6-hydroxynorketamine, or a pharmaceutically acceptable salt thereof, and cannabis or cannabinoids are co-formulated into a sublingual dosage form, and (ii) the sublingual dosage form is administered sublingually. In certain embodiments, the sublingual dosage form is selected from a film, a strip, a lozenge, and an orally dissolving tablet.

[0021] In some embodiments, the cannabis or cannabinoid comprises at least one of delta-9-THC, delta-8-THC, cannabinol (CBN), delta-9-THCV, delta-8-THCV, cannabidiol (CBD), and cannabivarin (CBV).

[0022] In some embodiments of any of the above methods, the method includes administering to the subject one or more doses of delta-9-THC between 1 mg and 40 mg (e.g., between 1 mg and 5 mg, between 2 mg and 15 mg, between 5 mg and 20 mg, between 7 mg and 25 mg, or between 10 mg and 40 mg). In certain embodiments, the method includes administering to the subject an average daily dose of delta-9-THC between 2 mg and 100 mg (e.g., 4±2 mg, 7.5±2.5 mg, 15±5 mg, 25±5 mg, 35±5 mg, 45±5 mg, 55±5 mg, 65±5 mg, or 75±25 mg).

[0023] In some embodiments of any of the above methods, the method includes administering to the subject one or more doses of delta-8-THC between 1 mg and 80 mg (e.g., between 1 mg and 5 mg, between 2 mg and 15 mg, between 5 mg and 20 mg, between 7 mg and 25 mg, between 10 mg and 40 mg, between 20 mg and 50 mg, between 40 mg and 70 mg, between 50 mg and 80 mg). In certain embodiments, the method includes administering to the subject an average daily dose of delta-8-THC between 2 mg and 100 mg (e.g., 4±2 mg, 7.5±2.5 mg, 15±5 mg, 25±5 mg, 35±5 mg, 45±5 mg, 55±5 mg, 65±5 mg, or 75±25 mg).

[0024] In some embodiments of any of the above methods, the method includes administering to the subject one or more doses of CBN between 1 mg and 30 mg (e.g., between 1 mg and 5 mg, between 2 mg and 15 mg, between 5 mg and 20 mg, between 7 mg and 25 mg, or between 10 mg and 30 mg). In certain embodiments, the method includes administering to the subject an average daily dose of CBN between 2 mg and 100 mg (e.g., 4±2 mg, 7.5±2.5 mg, 15±5 mg, 25±5 mg, 35±5 mg, 45±5 mg, 55±5 mg, 65±5 mg, or 75±25 mg).

[0025] In some embodiments of any of the above methods, the method includes administering to the subject one or more doses of delta-9-THCV between 1 mg and 30 mg (e.g., between 1 mg and 5 mg, between 2 mg and 15 mg, between 5 mg and 20 mg, between 7 mg and 25 mg, or between 10 mg and 30 mg). In certain embodiments, the method includes administering to the subject an average daily dose of delta-9-THCV between 2 mg and 100 mg (e.g., 4±2 mg, 7.5±2.5 mg, 15±5 mg, 25±5 mg, 35±5 mg, 45±5 mg, 55±5 mg, 65±5 mg, or 75±25 mg).

[0026] In some embodiments of any of the above methods, the method includes administering to the subject one or more doses of delta-8-THCV between 1 mg and 30 mg (e.g., between 1 mg and 5 mg, between 2 mg and 15 mg, between 5 mg and 20 mg, between 7 mg and 25 mg, or between 10 mg and 30 mg). In certain embodiments, the method includes administering to the subject an average daily dose of delta-8-THCV between 2 mg and 100 mg (e.g., 4±2 mg, 7.5±2.5 mg, 15±5 mg, 25±5 mg, 35±5 mg, 45±5 mg, 55±5 mg, 65±5 mg, or 75±25 mg).

[0027] In some embodiments of any of the above methods, the method includes administering to the subject one or more doses of CBD between 10 mg and 800 mg (e.g., between 10 mg and 50 mg, between 20 mg and 150 mg, between 50 mg and 200 mg, between 70 mg and 250 mg, between 100 mg and 400 mg, between 200 mg and 500 mg, between 400 mg and 700 mg, between 500 mg and 800 mg). In certain embodiments, the method includes administering to the subject an average daily dose of CBD between 20 mg and 1,000 mg (e.g., 40±20 mg, 75±25 mg, 150±50 mg, 250±50 mg, 350±50 mg, 450±50 mg, 550±50 mg, 650±50 mg, or 750±250 mg).

[0028] In some embodiments of any of the above methods, the method includes administering to the subject one or more doses of CBV between 1 mg and 30 mg (e.g., between 1 mg and 5 mg, between 2 mg and 15 mg, between 5 mg and 20 mg, between 7 mg and 25 mg, or between 10 mg and 30 mg). In certain embodiments, the method includes administering to the subject an average daily dose of CBV between 2 mg and 100 mg (e.g., 4±2 mg, 7.5±2.5 mg, 15±5 mg, 25±5 mg, 35±5 mg, 45±5 mg, 55±5 mg, 65±5 mg, or 75±25 mg).

[0029] definition As used herein, the term "average daily dose" refers to the average amount of ketamine, norketamine, 6-hydroxynorketamine, or its pharma- ceutically acceptable salt, and cannabis or cannabinoids that are co-administered to a subject for a given dosing regimen.For example, when 100 mg of ketamine is administered once every other day, the average daily dose is 50 mg.For a regimen in which 15 mg of ketamine is administered twice a day, the average daily dose is 30 mg.

[0030] As used herein, "beverage" refers to a fluid suitable for consumption, such as tea, soda, or soft drink.

[0031] As used herein, "cannabis" refers to material of any species or subspecies of the cannabis plant, particularly the flower buds of any species or subspecies of the cannabis plant, and any product or substance made from cannabis plant material that contains at least one cannabinoid compound.

[0032] As used herein, "cannabis oil" refers to a liquid mixture of compounds obtained from the extraction of the cannabis plant. Such compounds include, but are not limited to, cannabinoids. The exact composition of cannabis oil varies depending on the strain of cannabis used for extraction, the efficiency and method of the extraction itself, and any additives that may be incorporated to modify the taste or improve the administration of the cannabis oil.

[0033] As used herein, "cannabis concentrate" refers to a solid, semi-solid, or waxy mixture of compounds obtained from the extraction of the cannabis plant. Such compounds include, but are not limited to, cannabinoids. The exact composition of the cannabis concentrate varies depending on the strain of cannabis used for extraction, as well as the efficiency and method of the extraction itself.

[0034] As used herein, "cannabinoid" refers to a class of chemical compounds that act on cannabinoid receptors.Cannabinoids found in cannabis include, but are not limited to, cannaigre, cannabichromene (CBC), cannabidiol (CBD), tetrahydrocannabinol (THC) (e.g., delta-9-THC or delta-8-THC), cannabinol (CBN) and cannabinodiol (CBDL), cannabicyclol (CBL), cannabivarin (CBV), tetrahydrocannabivarin (THCV), cannabidivarin (CBDV), cannabichromevarin (CBCV), cannabigerovarin (CBGV), cannabigerol monomethyl ether (CBGM), cannabinerolic acid, cannabidiolic acid (CBDA), cannabinol propyl variant (CBNV), cannabiditriol (CBO), tetrahydrocannabinolic acid (THCA), and tetrahydrocannabivarinic acid (THCVA).

[0035] As used herein, "foodstuff" refers to an edible substance, such as a baked good (e.g., a cookie or brownie), a candy, a snack, or a meal (e.g., breakfast, lunch, or dinner).

[0036] As used herein, "high THC content subspecies" refers to a Cannabis subspecies lineage having 20% ​​or more THC by dry weight.

[0037] As used herein, "high CBD content subspecies" refers to a Cannabis subspecies having 1% or more CBD by dry weight.

[0038] As used herein, the term "pharmaceutically acceptable salts" refers to salts of active compounds of the present invention, which can be prepared in situ during the final isolation and purification of the compounds of the present invention, or separately by reacting a free base functional group with a suitable organic or inorganic acid, or by reacting an acid functional group with a suitable organic or inorganic base.

[0039] A "therapeutically effective amount" or "sufficient amount" of a drug is an amount effective to exhibit the desired activity of the drug. According to the present invention, a therapeutically effective amount of ketamine and / or cannabis or cannabinoid is an amount effective to alleviate, i.e., significantly reduce, the symptoms of an emotional disorder. The therapeutically effective amount of ketamine or cannabis or cannabinoid, when administered in combination, may be less than the therapeutically effective amount of either ketamine or cannabis or cannabinoid administered alone.

[0040] As used herein, "topical composition" means, for example, an ointment, cream, lotion, paste, gel, etc., that releases at least one compound at a defined rate over a defined period of time to a defined site of application.

[0041] As used herein, the term "treating" refers to administering a pharmaceutical composition for therapeutic purposes. Use to "treat a disease" or for "therapeutic treatment" refers to administering a treatment to a subject already suffering from a condition in order to improve or stabilize the subject's condition.

[0042] As used herein, the term "vaporized" means converted into a vapor and / or aerosol by the application of heat. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0043] The present invention provides for the first time a method for treating an emotional disorder by co-administration of ketamine and cannabis or a cannabinoid. The present invention further provides a method for treating the physical symptoms of an emotional disorder by co-administration of ketamine and cannabis or a cannabinoid. The emotional disorder treated by this method can be an anxiety disorder. The emotional disorder treated by this method can be a depressive disorder.

[0044] The compositions of the invention may be designed to be short-acting, fast-releasing, long-acting, or sustained-releasing, as described herein. Thus, the pharmaceutical formulations may be formulated for controlled or sustained release.

[0045] Anxiety is broadly defined as a state of unfounded or inappropriate worry, often accompanied by restlessness, tension, distractibility, irritability, and sleep disturbance. This disproportionate response to environmental stimuli can overactivate the hypothalamic-pituitary-adrenal axis and the autonomic nervous system, resulting in physical symptoms of anxiety, including shortness of breath, sweating, nausea, tachycardia, and elevated blood pressure. Anxiety disorders represent a range of conditions and have consequently been classified into several distinct conditions, including generalized anxiety disorder (GAD), panic disorder (PD), social anxiety disorder (SAD), obsessive-compulsive disorder (OCD), specific phobia disorder (SPD), post-traumatic stress disorder (PTSD), agoraphobia, or separation anxiety disorder (SeAD). GAD is the most commonly occurring anxiety disorder and is characterized by excessive and persistent worry. In the general population, the lifetime prevalence of GAD ranges from 4.1 to 6.6%, with a somewhat higher rate in women than in men. Individuals with GAD worry about life events, such as marital status, job performance, health, money, and social status. Individuals with GAD may be easily startled and suffer from depression. Some of the specific symptoms of GAD include restlessness, motor tension, difficulty concentrating, and irritability. Symptom severity may be related to variability in environmental stressors over time. With increasing age, GAD symptoms become less severe. PD is a well-studied psychiatric condition consisting of multiple disabling panic attacks characterized by intense autonomic arousal. In addition, heightened states of fear and anxiety occur both during and between panic attacks. Approximately 3% of women and 1.5% of men have panic attacks. During a panic attack, individuals experience multiple symptoms, including lightheadedness, racing heart, and difficulty breathing. SAD is a chronic disorder in which social interactions cause irrational anxiety. Individuals with SAD may experience heightened anxiety, fear, self-consciousness, and embarrassment during everyday social interactions. Individuals with SAD may experience fear of being embarrassed, judged, and / or rejected during everyday social interactions.OCD is a common chronic persistent disorder characterized by recurrent irrational thoughts and fears (e.g., obsessions) that lead to compulsive behaviors. Individuals with OCD may experience irrational fears of germs or contamination, undesirable thoughts that are not allowed or taboo, aggressive thoughts towards themselves or others, or an obsessive desire to arrange things in a symmetrical or perfect order. Individuals with OCD may engage in compulsive behaviors. Exemplary, non-limiting compulsive behaviors include excessive cleaning and / or hand washing, arranging or placing things in a specific, precise way, repeatedly checking whether a task is complete (e.g., whether the door is locked or the oven is turned off), or compulsive counting. SPD is a class of disorders characterized by persistent, unrealistic, intense anxiety and fear about specific situations, environments, and objects. Non-limiting examples of situations, environments, and objects that individuals with SPD may be anxious or afraid of include animals, heights, or thunderstorms. PTSD is an anxiety disorder that occurs in people who have experienced or witnessed a traumatic event. Non-limiting examples of traumatic events that may cause PTSD in individuals include serious accidents, acts of terrorism, war and / or combat, sexual violence or the threat of imminent death, sexual violence, or serious injury. Individuals with PTSD may experience disturbing and intense thoughts or emotions related to the traumatic experience that continue long after the traumatic event has ended. Non-limiting examples of disturbing and intense thoughts or emotions include flashbacks or nightmares, feelings of grief, fear, or anger, and feelings of isolation and / or alienation from others. Agoraphobia is an anxiety disorder characterized by fear of situations that are perceived as unsafe and unavoidable. Non-limiting examples of situations that an individual suffering from agoraphobia may fear include traveling on public transportation, going to a shopping center, being in a crowd, being in an open space, being in an enclosed space, waiting in line, or being away from home.SeAD is an anxiety disorder characterized by excessive fear, anxiety, and distress about being separated from home or loved ones. Non-limiting examples of fears that individuals with SeAD may experience include fear of losing a parent or other loved one due to illness or disaster, or fear that something bad (e.g., getting lost or kidnapped) may happen in the future that causes them to be separated from their home and / or loved ones.

[0046] Depressive disorders are broadly defined as serious mood disorders characterized by sadness that is severe enough or persistent enough to interfere with functioning, and often by a decreased interest in the pleasures of activity. The origin of depressive disorders likely involves a combination of genetic factors, altered neurotransmitter levels, altered neuroendocrine function, and psychosocial factors. Depressive disorders represent a range of conditions, and as a result are classified into several distinct conditions, including but not limited to dysthymia, major depression, bipolar II disorder, and adjustment disorder with depression. Dysthymia, also known as persistent depressive disorder (PDD), is a chronic depressive disorder characterized by symptoms of depression that continue for at least two years. Non-limiting examples of symptoms that individuals suffering from dysthymia may experience include decreased appetite or overeating, changes in sleep patterns (e.g., insomnia or hypersomnia), decreased energy or fatigue, decreased self-esteem, decreased concentration or difficulty making decisions, or feelings of hopelessness. Major depression is a depressive mood disorder characterized by a persistently low mood that causes significant impairment in daily life.Non-limiting examples of symptoms that individuals suffering from major depression may experience include: low mood, loss of interest or pleasure in almost all activities, significant unintentional weight gain or loss (e.g., weight loss of more than 5% in one month), sleep disorder (e.g., insomnia or hypersomnia), psychomotor changes that are severe enough to be observable by others (e.g., agitation or slowness), fatigue, tiredness or reduced energy, reduced efficiency in completing daily tasks, feelings of worthlessness or inadequacy, delusional guilt, reduced ability to think, concentrate or make decisions, recurring thoughts of death, suicidal ideation, or suicide attempts.Bipolar II disorder is a depressive disorder characterized by a pattern of depressive and hypomanic episodes. Non-limiting examples of symptoms that an individual with bipolar II disorder may experience during a depressive episode include feelings of sadness, emptiness or hopelessness, decreased motivation, loss of interest in activities, sleep disturbances (e.g., insomnia or hypersomnia), decreased energy, feelings of worthlessness or guilt, difficulty concentrating, unintentional weight loss or gain, or suicidal thoughts.Non-limiting examples of symptoms that an individual suffering from bipolar II disorder may experience during a hypomanic episode include increased energy, activity, or agitation, a sense of well-being and inflated self-esteem, decreased need for sleep, unusual talkativeness, racing thoughts, distractibility, or impaired decision-making ability.Adjustment disorder with depression is a depressive disorder characterized by the onset of emotional or behavioral symptoms in response to a identifiable stressor occurring within three months of the onset of the stressor.Non-limiting examples of symptoms that an individual suffering from adjustment disorder with depression may experience include low mood, tearfulness, or feelings of hopelessness.

[0047] Individuals suffering from emotional disorders, such as anxiety and / or depressive disorders, may experience physical symptoms of the disorder. Non-limiting examples of physical symptoms experienced by individuals suffering from emotional disorders include body pain, headaches, joint pain, nausea, vomiting, fatigue, weakness, numbness, difficulty breathing, or shortness of breath.

[0048] Ketamine is a low-cost, readily available drug with few adverse side effects. Thus, the present invention contemplates further savings to the overburdened health care system. Sublingual administration of the drug is rapid, allowing for rapid action of the drug, and can be safely administered under medical supervision by non-medically trained practitioners, by MDs or other medically qualified practitioners, and under close supervision in a program that is easily accomplished and conducted at home. Intramuscular (IM) administration is a fast-acting method for improving the symptoms described herein. Other methods of administration are not excluded from the present invention.

[0049] Cannabis is a medicinal plant that naturally produces bioactive compounds, including cannabinoids.Cannabis and cannabinoids are generally non-toxic and have minimal adverse side effects.The present invention contemplates the use of all Cannabis species and subspecies, and all cannabinoids produced by Cannabis species and subspecies.The majority of states in the United States recognize the therapeutic value of cannabis and have legalized its medicinal use.

[0050] Ketamine and Norketamine The methods of the invention include the step of administering ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof.

[0051] [ka]

[0052] As used herein, the term "ketamine" includes ketamine in its racemic (R / S) form, its R-(-) enantiomerically pure form, or its S-(+) enantiomerically pure form.

[0053] As used herein, the term "norketamine" includes norketamine in its racemic (R / S) form, its R-(-) enantiomerically pure form, or its S-(+) enantiomerically pure form.

[0054] As used herein, "enantiomerically pure" refers to a composition that consists substantially of a single isomer (i.e., substantially free of the opposite isomer), preferably consisting of 90%, 92%, 95%, 98%, 99%, or 100% (w / w) of a single isomer. For example, when the method of the present invention includes a step of administering enantiomerically pure R-(-)-ketamine, the administered pharmaceutical composition can include at least 95% (w / w) S-(+)-ketamine and less than 5% (w / w) R-(-)-ketamine.

[0055] Ketamine racemate is primarily used for the induction and maintenance of general anesthesia. Enantiomerically pure S-(+)-ketamine (also known as esketamine) is available for medical use and is administered IV (intravenously) or IM (intramuscularly) under the trade name KETANEST®. Enantiomerically pure R-(-)-ketamine is also known as arketamine. Ketamine is metabolically converted in vivo by demethylation to norketamine at a rate that depends on the route of administration. For use in anesthesia, S-(+)-ketamine has been reported to be twice as potent as R-(-)-ketamine, and norketamine has been reported to be one-third as potent as ketamine (CST Aun, Br. J. Anaesthesia 83: 29-41 (1999)).

[0056] As used herein, the term "6-hydroxynorketamine" includes 6-hydroxynorketamine (shown below) in any of its 2R,6R, 2S,6S, 2S,6R, and 2R,6S isomerically pure forms.

[0057] [ka]

[0058] As used herein, "isomerically pure" refers to a composition that consists substantially of a single diastereomer (i.e., substantially free of other isomers), preferably consisting of 90%, 92%, 95%, 98%, 99%, or 100% (w / w) of a single isomer. For example, when the method of the present invention comprises administering isomerically pure (2R,6R)-6-hydroxynorketamine, the administered pharmaceutical composition can comprise at least 95% (w / w) (2R,6R)-6-hydroxynorketamine and less than 5% (w / w) of other isomers of 6-hydroxynorketamine. Alternatively, when the method of the present invention comprises administering isomerically pure (2S,6S)-6-hydroxynorketamine, the administered pharmaceutical composition can comprise at least 95% (w / w) (2S,6S)-6-hydroxynorketamine and less than 5% (w / w) of other isomers of 6-hydroxynorketamine.

[0059] Cannabis and cannabinoid compounds The method of the present invention includes administering cannabis. Cannabis, commonly known as marijuana, is a genus of flowering plants that includes at least three species: Cannabis sativa, Cannabis indica, and Cannabis ruderalis. Cannabis speciation is determined by plant phenotype and secondary metabolite profiles. Modern advances in cannabis cultivation have led to the development of subspecies or "strains" of cannabis that have characteristics of both sativa and indica species. Such strains are referred to herein as "hybrid strains."

[0060] Cannabinoids are a group of compounds produced by cannabis species that activate cannabinoid receptors (i.e., CB1 and CB2) in cells. Certain cannabinoids are psychoactive. At least 113 different cannabinoids have been identified in the cannabis plant. Cannabinoids can easily cross the blood-brain barrier and have few side effects. Most notable cannabinoids are (-)-trans-Δ 9-Tetrahydrocannabinol (Delta-9-THC), (-)-trans-Δ 8 -Tetrahydrocannabinol (delta-8-THC), cannabinol (CBN), tetrahydrocannabivarin (THCV), and cannabidiol (CBD).

[0061] The methods of the present invention include administering any cannabinoid-containing product produced from any strain of cannabis, as well as administering synthetic cannabinoids.

[0062] Formulation of pharmaceutical compositions Administration of ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof, and cannabis or cannabinoids may be by any suitable means to alleviate emotional disorders. Ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof, and cannabis or cannabinoids may be contained in any suitable amount in any suitable carrier substance, and are generally present in an amount of 1-95% by weight of the total weight of the composition. The composition may be provided in a dosage form suitable for sublingual, buccal, oral, parenteral (e.g., intravenous, intramuscular), pulmonary, intranasal, transdermal, vaginal, or rectal administration routes. Thus, the composition may be in the form of, for example, tablets, capsules, pills, powders, granules, suspensions, emulsions, solutions, gels, including hydrogels, pastes, ointments, creams, plasters, drenches, osmotic delivery devices, suppositories, enemas, injections, sprays, inhalants, or aerosols.The pharmaceutical composition may be formulated according to conventional pharmaceutical practice (see, for example, Remington: The Science and Practice of Pharmacy (20th ed.), ed. AR Gennaro, Lippincott Williams & Wilkins, 2000 and Encyclopedia of Pharmaceutical Technology, eds. J. Swarbrick and JC Boylan, 1988-1999, Marcel Dekker, New York).

[0063] The pharmaceutical compositions according to the present invention can be formulated to release the active compound substantially immediately upon administration or at any predetermined time or period after administration. The latter type of composition is generally known as a controlled release formulation and includes (i) formulations that produce a substantially constant concentration of the active compound in the body over an extended period of time, (ii) formulations that produce a substantially constant concentration of the active compound in the body over an extended period of time after a predetermined time lag, and (iii) formulations that sustain the action of the active compound over a predetermined period of time by maintaining a relatively constant effective level of the active compound in the body while minimizing undesirable side effects associated with fluctuations in the plasma level of the active compound (sawtooth kinetic pattern).

[0064] Administration of ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof, and cannabis or a cannabinoid in the form of a controlled release formulation is particularly preferred when the active compound alone, or the combination of the active compound with a second agent, results in undesirable side effects, such as nausea, at therapeutic levels.

[0065] In order to control release the active compound of interest, any of several strategies can be explored. In one example, controlled release is obtained by appropriately selecting various formulation parameters and ingredients, including, for example, various types of controlled release compositions and coatings. Thus, drugs are formulated with appropriate excipients into pharmaceutical compositions that release the active compound in a controlled manner upon administration. Examples include single or multiple unit tablet or capsule compositions, oil solutions, suspensions, emulsions, microcapsules, microspheres, nanoparticles, patches, and liposomes.

[0066] Sublingual and buccal dosage forms Sublingual formulations can be in the form of films, strips, lozenges, and orally dissolving tablets. Orally dissolving tablets (ODT) refer to pharmaceutical dosage forms that are designed to dissolve on the tongue rather than being swallowed whole, or that are designed to dissolve sublingually or on the oral mucosa for sublingual or mucosal administration. Alternatively, the dosage form can be a lozenge (as a lozenge that dissolves over 5-10 minutes for slower administration), or a fast-dissolving film (dissolves in less than 2 minutes). The active compound is administered by absorption in the mouth (i.e., buccal or sublingual). The excipients of the formulation are edible and pharma- ceutically acceptable, using excipients known in the art for the preparation of films, strips, lozenges, and orally dissolving tablets. For example, films are typically prepared using hydrophilic polymers that dissolve rapidly on the tongue, on the palate tissue, or in the oral cavity by dissolving upon contact with liquid, delivering the active compound to the systemic circulation.

[0067] Solid dosage forms for oral use Formulations for oral use include tablets containing the active ingredient(s) in a mixture with non-toxic pharma- ceutically acceptable excipients. These excipients may be, for example, inert diluents or fillers (e.g., sucrose, sorbitol, sugar, mannitol, microcrystalline cellulose, starches including potato starch, calcium carbonate, sodium chloride, lactose, calcium phosphate, calcium sulfate, or sodium phosphate), granulating and disintegrating agents (e.g., cellulose derivatives including microcrystalline cellulose, starches including potato starch, croscarmellose sodium, alginates, or alginic acid), binders (e.g., sucrose, glucose, sorbitol, acacia, alginic acid, sodium alginate, gelatin, starch, pregelatinized starch, microcrystalline cellulose, magnesium aluminum silicate, sodium carboxymethylcellulose, methylcellulose, hydroxypropylmethylcellulose, ethylcellulose, polyvinylpyrrolidone, or polyethylene glycol), as well as lubricants, glidants, and anti-adherents (e.g., magnesium stearate, zinc stearate, stearic acid, silica, hydrogenated vegetable oils, or talc). Other pharma- ceutically acceptable excipients can be colorants, flavoring agents, plasticizers, humectants, buffering agents, and the like.

[0068] The tablets may be uncoated or may be coated by known techniques, optionally to delay disintegration and absorption in the gastrointestinal tract, thereby providing a sustained action over a longer period of time. The coating may be adapted to release the active compound in a predetermined pattern (e.g., to achieve a controlled release formulation) or may be adapted not to release the active compound until after passage through the stomach (enteric coating). The coating may be sugar coating, film coating (e.g., based on hydroxypropylmethylcellulose, methylcellulose, methylhydroxyethylcellulose, hydroxypropylcellulose, carboxymethylcellulose, acrylate copolymers, polyethylene glycol and / or polyvinylpyrrolidone), or enteric coating (e.g., based on methacrylic acid copolymers, cellulose acetate phthalate, hydroxypropylmethylcellulose phthalate, hydroxypropylmethylcellulose acetate succinate, polyvinyl acetate phthalate, shellac, and / or ethylcellulose). Additionally, time-delay materials, such as glyceryl monostearate or glyceryl distearate, may be used.

[0069] The solid tablet composition may include a coating adapted to protect the composition from undesired chemical changes (e.g., chemical degradation prior to the release of the active compound). Coatings may be applied to solid dosage forms in a manner similar to that described in the Encyclopedia of Pharmaceutical Technology, supra.

[0070] In combination therapy, the two drugs can be mixed together in a tablet or can be kept separate. In one example, a first drug is contained on the inside of the tablet and a second drug is on the outside, thus allowing a substantial portion of the second drug to be released before the first drug is released.

[0071] Formulations for oral use may be presented as chewable tablets or as hard gelatin capsules (wherein the active compound is mixed with an inert solid diluent (e.g., potato starch, lactose, microcrystalline cellulose, calcium carbonate, calcium phosphate, or kaolin)) or as soft gelatin capsules (wherein the active compound is mixed with water or an oil medium, for example, peanut oil, liquid paraffin, or olive oil). Powders and granules can be prepared in a conventional manner, for example using mixers, fluid bed apparatus, or spray drying equipment, using the ingredients mentioned above for the tablets and capsules. Formulations for oral use may include cannabis or cannabinoids in food form (e.g., cannabis-infused gummy bears or cookies), or in drink form.

[0072] Pulmonary Administration Cannabis is generally administered via pulmonary administration, for example by smoking or vaporizing cannabis plant material, cannabis oil, or cannabis concentrate.For example, cannabis plant material can be rolled into cigarettes and smoked, or smoked from a pipe or other device.Cannabis plant material, oil, or concentrate can be placed in an electronic inhalation device, sometimes collectively referred to as a vaporizer or e-cigarette, which vaporizes and / or aerosolizes cannabis compounds, e.g., cannabinoids, to deliver said compounds in an inhalable form.

[0073] Controlled release oral dosage forms Controlled release compositions for oral use may, for example, be constructed to release the active compound by controlling the dissolution and / or diffusion of the active drug substance.

[0074] Dissolution or diffusion controlled release can be achieved by suitable coating of the compound's tablet, capsule, pellet, or granule formulation, or by incorporating the compound into a suitable matrix. Controlled release coatings can include one or more of the coating materials mentioned above, and / or, for example, shellac, beeswax, glycowax™, castor wax, carnauba wax, stearyl alcohol, glyceryl monostearate, glyceryl distearate, glycerol palmitostearate, ethyl cellulose, acrylic resins, dl-polylactic acid, cellulose acetate butyrate, polyvinyl chloride, polyvinyl acetate, vinylpyrrolidone, polyethylene, polymethacrylate, methyl methacrylate, 2-hydroxymethacrylate, methacrylate hydrogel, 1,3 butylene glycol, ethylene glycol methacrylate, and / or polyethylene glycol. In controlled release matrix formulations, the matrix material may include, for example, hydrated methylcellulose, carnauba wax and stearyl alcohol, carbopol™ 934, silicone, glyceryl tristearate, methyl acrylate-methyl methacrylate, polyvinyl chloride, polyethylene, and / or halogenated fluorocarbons.

[0075] A controlled release composition containing one or more of the compounds of the claimed combination may be in the form of a buoyant tablet or capsule (i.e., a tablet or capsule that, when administered orally, floats on top of the gastric contents for a period of time). A buoyant tablet formulation of the compound can be prepared by granulating a mixture of the drug(s) with excipients and 20-75 w / w% of a hydrocolloid, such as hydroxyethylcellulose, hydroxypropylcellulose, or hydroxypropylmethylcellulose. The resulting granules can then be compressed into a tablet. Upon contact with gastric fluid, the tablet forms a substantially water-impermeable gel barrier around its surface. This gel barrier is responsible for maintaining a density of less than 1, thereby allowing the tablet to remain buoyant in gastric fluid.

[0076] Liquid for oral administration Powders, dispersible powders, or granules suitable for preparing aqueous suspension by adding water are convenient dosage forms for oral administration. Formulation as suspension provides active compound in a mixture with dispersing or wetting agent, suspending agent, and one or more preservatives. Suitable dispersing or wetting agents are, for example, naturally occurring phosphatides (e.g., lecithin, or condensation products of ethylene oxide with fatty acids, long chain aliphatic alcohols, or partial esters derived from fatty acids) and hexitol or hexitol anhydrides (e.g., polyoxyethylene stearate, polyoxyethylene sorbitol monooleate, polyoxyethylene sorbitan monooleate, etc.). Suitable suspending agents are, for example, sodium carboxymethylcellulose, methylcellulose, sodium alginate, etc.

[0077] Parenteral Compositions Pharmaceutical compositions containing ketamine, norketamine, 6-hydroxynorketamine, or pharma- ceutically acceptable salts thereof may be administered parenterally by injection, infusion, or implant (intravenous, intramuscular, subcutaneous, etc.) in dosage forms, formulations containing conventional non-toxic pharma- ceutically acceptable carriers and adjuvants, or via suitable delivery devices or implants. The formulations and preparations of such compositions are well known to those skilled in the art of pharmaceutical formulation. Formulations can be found in Remington: The Science and Practice of Pharmacy, supra.

[0078] Compositions for parenteral use can be provided in unit dosage form (e.g., in single-dose ampoules) or in vials containing multiple doses, in which suitable preservatives can be added (see below). The compositions can be in the form of solutions, suspensions, emulsions, injection devices, or delivery devices for implants, or presented as dry powders to be reconstituted with water or another suitable vehicle before use. The compositions can contain suitable parenterally acceptable carriers and / or excipients apart from the active compound. The active drug can be incorporated into microspheres, microcapsules, nanoparticles, liposomes, etc. for controlled release. In addition, the compositions can contain suspending agents, solubilizing agents, stabilizing agents, pH adjusting agents, and / or dispersing agents.

[0079] As mentioned above, the pharmaceutical composition according to the present invention can be in a form suitable for sterile injection. To prepare such a composition, the suitable active compound is dissolved or suspended in a parenterally acceptable liquid vehicle. Acceptable vehicles and solvents that can be used include water, water adjusted to a suitable pH by adding an appropriate amount of hydrochloric acid, sodium hydroxide, or a suitable buffer, 1,3-butanediol, Ringer's solution, and isotonic sodium chloride solution. Aqueous preparations may contain one or more preservatives (e.g., methyl, ethyl, or n-propyl p-hydroxybenzoate).

[0080] Controlled release parenteral compositions Controlled release parenteral compositions can be in the form of aqueous suspensions, microspheres, microcapsules, magnetic microspheres, oily solutions, oily suspensions, or emulsions. Alternatively, the active drug can be incorporated into biocompatible carriers, liposomes, nanoparticles, implants, or infusion devices.

[0081] Materials for use in the preparation of microspheres and / or microcapsules are, for example, biodegradable / biodegradable polymers, such as polyglactin, poly-(isobutylcyanoacrylate), poly(2-hydroxyethyl-L-glutamine), and poly(lactic acid). Biocompatible carriers that may be used when formulating controlled release parenteral formulations are carbohydrates (e.g., dextran), proteins (e.g., albumin), lipoproteins, or antibodies. Materials for use in implants may be non-biodegradable (e.g., polydimethylsiloxane) or biodegradable (e.g., poly(caprolactone), poly(lactic acid), poly(glycolic acid), or poly(orthoesters)).

[0082] Rectal composition For rectal application, the suitable dosage form of the composition includes suppositories (emulsion or suspension type) and rectal gelatin capsules (solution or suspension).In typical suppository preparations, active compound is mixed with suitable pharmaceutically acceptable suppository base, such as cocoa butter, esterified fatty acid, glycerinated gelatin, and various water-soluble or dispersible bases, such as polyethylene glycol and polyoxyethylene sorbitan fatty acid ester.Various additives, enhancers, or surfactants can be incorporated.

[0083] Vaginal Composition For vaginal application, the suitable dosage form of the composition includes suppositories (emulsion or suspension type) and vaginal gelatin capsules (solution or suspension).In typical suppository preparations, active compound is mixed with suitable pharma- ceutically acceptable suppository base, such as cocoa butter, esterified fatty acid, glycerinated gelatin, and various water-soluble or dispersible bases, such as polyethylene glycol and polyoxyethylene sorbitan fatty acid ester.Various additives, enhancers, or surfactants can be incorporated.

[0084] Intranasal and inhalation compositions For administration by inhalation, typical dosage forms include nasal sprays and aerosols.In typical nasal formulations, active compound is dissolved or dispersed in a suitable vehicle.The pharmaceutically acceptable vehicle and excipients (as well as other pharmaceutically acceptable substances present in the composition, such as diluents, enhancers, flavorings, and preservatives) are selected according to conventional pharmaceutical practice and in a manner understood by those skilled in the art of formulating pharmaceuticals.

[0085] Transdermal and Topical Compositions The pharmaceutical compositions may be co-administered topically to the skin for percutaneous absorption in dosage forms or formulations, including microspheres and liposomes, containing conventional non-toxic pharma- ceutically acceptable carriers and excipients. Formulations include creams, ointments, lotions, liniments, gels, hydrogels, solutions, suspensions, sticks, sprays, pastes, plasters, and other types of transdermal drug delivery systems. Pharmaceutically acceptable carriers or excipients may include emulsifiers, antioxidants, buffers, preservatives, humectants, penetration enhancers, chelating agents, gel-forming agents, ointment bases, flavorings, and skin protectants.

[0086] Examples of emulsifiers are naturally occurring gums (e.g., gum acacia or gum tragacanth) and naturally occurring phosphatides (e.g., soy lecithin and sorbitan monooleate derivatives). Examples of antioxidants are butylated hydroxyanisole (BHA), ascorbic acid and its derivatives, tocopherol and its derivatives, butylated hydroxyanisole, and cysteine. Examples of preservatives include parabens, such as methyl or propyl p-hydroxybenzoate, and benzalkonium chloride. Examples of humectants are glycerin, propylene glycol, sorbitol, and urea. Examples of penetration enhancers are propylene glycol, DMSO, triethanolamine, N,N-dimethylacetamide, N,N-dimethylformamide, 2-pyrrolidone and its derivatives, tetrahydrofurfuryl alcohol, and AZONE™. Examples of chelating agents are sodium EDTA, citric acid, and phosphoric acid. Examples of gel-forming agents are CARBOPOL™, cellulose derivatives, bentonite, alginates, gelatin and polyvinylpyrrolidone. Examples of ointment bases are beeswax, paraffin, cetyl palmitate, vegetable oils, sorbitan esters of fatty acids (Span), polyethylene glycols, and condensation products of sorbitan esters of fatty acids with ethylene oxide (e.g., polyoxyethylene sorbitan monooleate (TWEEN™)).

[0087] The composition may be adapted to be applied or introduced directly into the relevant opening of the body (e.g., the rectal, urethral, ​​vaginal or oral opening). The composition may be applied by using a special drug delivery device, such as a bandage or alternatively a plaster, pad, sponge, strip, or other form of suitable flexible material.

[0088] Dosage The dosages of co-administered ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof, and cannabis or cannabinoids will vary depending on several factors, including the method of administration, the condition or symptom being treated, the severity of the condition or symptom, whether the condition is being treated or prevented, and the age, weight, and health of the human being treated. In addition, pharmacogenomic (the effect of genotype on the pharmacokinetic, pharmacodynamic, or efficacy profile of a therapeutic drug) information about a particular patient may affect the dosages used.

[0089] As mentioned above, the active compound can be co-administered orally in the form of tablets, capsules, elixirs or syrups, or vaginally or rectally in the form of suppositories.The parenteral administration of the active compound is preferably carried out, for example, in the form of saline solution or when the compound is incorporated in liposomes.The sublingual or buccal administration of the active compound can be carried out in the form of films, strips, lozenges, and orally dissolving tablets.

[0090] The amount of ketamine, norketamine, 6-hydroxynorketamine, or pharma- ceutically acceptable salts thereof administered can be from about 0.01 mg (mg / kg) to about 5 mg / kg of active compound per kg of subject body weight (e.g., about 0.05 mg / kg to about 1 mg / kg, about 0.05 mg / kg to about 0.5 mg / kg, about 1 mg / kg to about 3 mg / kg, or about 2 mg / kg to about 5 mg / kg), depending on the route of administration. In general, doses range from about 10 mg / day to about 300 mg / day (e.g., about 25 mg / day to about 150 mg / day or about 50 mg / day to about 300 mg / day) for sublingual administration. Doses range from about 5 mg / day to about 100 mg / day (e.g., about 5 mg / day to about 50 mg / day or about 25 mg / day to about 100 mg / day) for intranasal administration. The dosage ranges from about 2 mg / day to about 75 mg / day (e.g., about 2 mg / day to about 35 mg / day or about 25 mg / day to about 75 mg / day) for intravenous administration. The dosage ranges from about 10 mg / day to about 75 mg / day (e.g., about 10 mg / day to about 45 mg / day or about 40 mg / day to about 75 mg / day) for intramuscular administration. The dosage ranges from about 50 mg / day to about 250 mg / day (e.g., about 50 mg / day to about 125 mg / day or about 100 mg / day to about 250 mg / day) for transdermal administration.

[0091] The amount of cannabinoid administered may range from 1 mg cannabinoid to 1,000 mg cannabinoid (e.g., 1 mg-50 mg, 2 mg-9 mg, 5 mg-15 mg, 10 mg-30 mg, 15 mg-50 mg, 25 mg-250 mg, 50 mg-500 mg, 250 mg-750 mg, or 750 mg-1,00 mg cannabinoid) depending on the cannabinoid and route of administration. For example, when the cannabis plant material is administered, for example, via pulmonary administration, the amount may range from 0.05 g cannabis plant material to 1 g plant material per subject, for example, 0.1 g plant material to 0.9 g plant material, 0.2 g plant material to 0.8 g plant material, 0.3 g plant material to 0.7 g plant material, 0.4 g plant material to 0.6 g plant material, or 0.5 g plant material. When a cannabis extract or concentrate, or a cannabis-containing foodstuff is administered, the dose may range from 1 mg THC to 10 mg THC (e.g., 1 mg to 50 mg, 2 mg to 9 mg, 5 mg to 15 mg, 10 mg to 30 mg, 15 mg to 50 mg) depending on the route of administration.

[0092] treatment Treatment according to the invention can be provided at home, in a doctor's office, clinic, outpatient hospital, or hospital. Treatment begins in the doctor's office so that the doctor can closely monitor the effectiveness of the treatment and make any adjustments that are needed. The duration of treatment will vary depending on the type and severity of the emotional disorder being treated, the age and condition of the patient, the stage and type of the patient's emotional disorder, and how the patient responds to the treatment.

[0093] Optionally, ketamine, norketamine, 6-hydroxynorketamine, or a pharmaceutically acceptable salt thereof, and cannabis or cannabinoids are co-administered in combination with additional agents (e.g., muscle relaxants or anti-inflammatory agents). For combination therapy, the dosage, frequency and method of administration of each component of the combination can be independently controlled. For example, ketamine, norketamine, 6-hydroxynorketamine, or a pharmaceutically acceptable salt thereof, and cannabis or cannabinoids can be co-administered sublingually in the regimen described herein, while the additional agent can be administered orally once a day. The combination of therapeutic agents may be formulated together to deliver all active agents in one administration. EXAMPLES

[0094] The following examples are put forth to provide one of ordinary skill in the art with an illustration of how the compositions and methods described herein can be used, made and evaluated, and are intended to be purely illustrative of the invention and are not intended to limit the scope of what the inventors regard as their invention.

[0095] [Example 1] Treatment of affective disorders with combined ketamine and cannabis therapy The combination of ketamine and THC-containing cannabis has been used at the Center for Transformational Psychotherapy clinic in hundreds of ketamine-assisted psychotherapy sessions over several years, both in the clinic and at home, in combination with sublingual ketamine lozenges and preceding intramuscular injections. This practice was possible within the legal framework of cannabis in California. The administration of cannabis was done through the use of an over-the-counter vaporizer, with full consent of the patients involved.

[0096] One of our embodiments includes cannabis in a form that dissolves within the same time range as ketamine, with the duration of effect being similar to or longer than that of ketamine. Cannabis can also be administered to subjects in small amounts through commercially available vaporizers immediately prior to administering ketamine through sublingual lozenges and nasal insufflation. For many patients who experience anxiety prior to a ketamine session, which can be dissociative in nature and disorienting, cannabis can help them relax into the ketamine experience. The alteration of the ketamine experience with cannabis has been reported to make the ketamine experience more colorful and open-minded. Cannabis has been reported to allow for a smoother return to reality. Cannabis has also been reported to enhance the depth of the ketamine experience, especially with regard to deep relaxation and relief from trauma. For some patients with limited ketamine experience, cannabis enhances the effects of ketamine with respect to depression and obsessive-compulsive states. Overall, patients report that the combination of cannabis and ketamine provides better outcomes for treating anxiety, depression or other emotional disorders, or is treated with less sedation compared to ketamine alone.

[0097] [Example 2] Combination therapy using sublingual ketamine and delta-8-THC In some embodiments, ketamine is combined with delta-8-THC in a sublingual dosage form to treat emotional disorders (e.g., reduce the severity of depression and / or anxiety). The effects of the combination therapy may include increased feelings of well-being, cheerfulness, relaxation, and / or positive affect in the subject. The dosage form may be formulated, for example, as a sublingual lozenge containing about 200 mg of S-(+)-ketamine and about 40 mg of delta-8-THC. The dosage form may be administered to the subject once a day or twice a day to improve symptoms of emotional disorders.

[0098] [Example 3] Combination therapy using oral ketamine and delta-8-THC In some embodiments, ketamine is combined with delta-8-THC in an oral dosage form to treat emotional disorders (e.g., reduce the severity of depression and / or anxiety). The effects of the combination therapy may include increased feelings of well-being, cheerfulness, relaxation, and / or positive affect in the subject. The dosage form may be formulated, for example, as a capsule containing about 200 mg of S-(+)-ketamine and about 40 mg of delta-8-THC. The dosage form may be administered to the subject once a day or twice a day to improve symptoms of emotional disorders.

[0099] [Example 4] Combination therapy using sublingual ketamine and delta-8-THCV In some embodiments, ketamine is combined with delta-8-THCV in a sublingual dosage form to treat emotional disorders (e.g., reduce the severity of depression and / or anxiety). The effects of the combination therapy may include increased feelings of well-being, cheerfulness, relaxation, and / or positive affect in the subject. The dosage form may be formulated, for example, as a sublingual lozenge containing about 200 mg of S-(+)-ketamine and about 25 mg of delta-8-THCV. The dosage form may be administered to the subject once a day or twice a day to improve symptoms of emotional disorders.

[0100] [Example 5] Combination therapy using oral ketamine and delta-8-THCV In some embodiments, ketamine is combined with delta-8-THCV in an oral dosage form to treat emotional disorders (e.g., reduce the severity of depression and / or anxiety). The effects of the combination therapy may include increased feelings of well-being, cheerfulness, relaxation, and / or positive affect in the subject. The dosage form may be formulated, for example, as a capsule containing about 200 mg of S-(+)-ketamine and about 25 mg of delta-8-THCV. The dosage form may be administered to the subject once a day or twice a day to improve symptoms of emotional disorders.

[0101] Other embodiments All publications, patents, and patent applications mentioned in this specification are herein incorporated by reference to the same extent as if each individual publication or patent application was specifically and individually indicated to be incorporated by reference.

[0102] While the invention has been described with respect to particular embodiments thereof, it will be understood that further modifications are possible, and this application is intended to cover any variations, uses, or adaptations of the invention which generally follow the principles of the invention and are within the scope of the claims, including such departures from the present disclosure as may be applicable to the essential features set forth hereinabove and which come within the known or customary practice in the art to which the invention pertains.

[0103] Other embodiments are within the scope of the following claims.

Claims

1. 1. A combination for use in a method for treating an emotional disorder in a subject in need thereof, the combination comprising: (i) ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof, and (ii) cannabis or a cannabinoid, each in amounts that are together effective to treat the emotional disorder.

2. 2. The combination of claim 1, wherein the mood disorder is an anxiety disorder.

3. 3. The combination of claim 2, wherein the anxiety disorder is selected from generalized anxiety disorder (GAD), panic disorder (PD), social anxiety disorder (SAD), obsessive-compulsive disorder (OCD), specific phobia disorder (SPD), post-traumatic stress disorder (PTSD), agoraphobia, or separation anxiety disorder (SeAD).

4. 2. The combination of claim 1, wherein the mood disorder is a depressive disorder.

5. 5. The combination of claim 4, wherein the depressive disorder is selected from dysthymia, major depression, bipolar II disorder, postpartum depression, or adjustment disorder accompanied by depression.

6. 2. The combination according to claim 1 for use in improving one or more physical symptoms associated with emotional disorders, wherein the physical symptoms are selected from headaches, migraines, physical symptoms related to the menstrual cycle such as breast tenderness, abdominal pain and headaches, symptoms of somatization disorders, fibromyalgia, various neurological symptoms and disorders, and pain from a wide variety of causes.

7. 7. The combination of any one of claims 1 to 6, wherein the cannabis is prepared from a cannabis strain selected from the group consisting of Cannabis indica, Cannabis sativa, hybrids, high tetrahydrocannabinol (THC) content cannabis strains, or high cannabidiol (CBD) content cannabis strains.

8. A combination described in any one of claims 1 to 6, wherein cannabis or a cannabinoid is administered to a subject by a route selected from oral, pulmonary, or transdermal administration.

9. 7. The combination of any one of claims 1 to 6, wherein ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof, and cannabis or a cannabinoid are administered by a route selected from oral, sublingual, intranasal, intramuscular, intravenous, transdermal, and rectal administration.

10. 7. The combination of any one of claims 1 to 6, wherein ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof is formulated into a lozenge.

11. 7. The combination of any one of claims 1 to 6, wherein ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof, and cannabis or a cannabinoid are co-administered once or more per day, once or more every other day, or once or more every third day, depending on the presence and / or severity of an emotional disorder, or the physical symptoms of an emotional disorder.

12. A combination described in any one of claims 1 to 6, wherein the method includes a step of initiating treatment after the subject experiences an emotional disorder or a physical symptom of an emotional disorder.

13. 7. The combination of any one of claims 1 to 6, wherein (i) ketamine, norketamine, 6-hydroxynorketamine, or a pharma- ceutically acceptable salt thereof, and (ii) cannabis or a cannabinoid are administered separately within 30 minutes of each other.

14. 7. The combination of any one of claims 1 to 6, wherein (i) ketamine, norketamine, 6-hydroxynorketamine, or a pharma-ceutically acceptable salt thereof, and cannabis or a cannabinoid are formulated together in a sublingual dosage form, and (ii) the sublingual dosage form is administered sublingually.

15. 7. The combination of any one of claims 1 to 6, wherein the cannabis or cannabinoid comprises at least one of delta-9-THC, delta-8-THC, cannabinol (CBN), tetrahydrocannabivarin (THCV), cannabidiol (CBD), and cannabivarin (CBV).