Classifications

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  • A61K31/445—Non condensed piperidines, e.g. piperocaine
  • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
  • A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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  • A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
  • A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
  • A61K31/216—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acids having aromatic rings, e.g. benactizyne, clofibrate
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  • A61K31/439—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom the ring forming part of a bridged ring system, e.g. quinuclidine
• • A—HUMAN NECESSITIES
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  • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
  • A61K31/445—Non condensed piperidines, e.g. piperocaine
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  • A61K31/445—Non condensed piperidines, e.g. piperocaine
  • A61K31/4468—Non condensed piperidines, e.g. piperocaine having a nitrogen directly attached in position 4, e.g. clebopride, fentanyl
• • A—HUMAN NECESSITIES
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  • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
  • A61K31/445—Non condensed piperidines, e.g. piperocaine
  • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
  • A61K31/4525—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with oxygen as a ring hetero atom
• • A—HUMAN NECESSITIES
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  • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
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  • A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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  • A61K31/50—Pyridazines; Hydrogenated pyridazines
  • A61K31/501—Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
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  • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
  • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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  • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
  • A61K31/5375—1,4-Oxazines, e.g. morpholine
  • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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  • A61P25/24—Antidepressants

Definitions

• the present invention relates to the use of a combination of a phosphodiesterase 4 inhibitor and one or more of a 5-HT4 agonist, an H3 antagonist or inverse agonist, a nicotinic a? receptor agonist, a
• depressive, anhedonia, motivation- related or cognition-related dysfunction such as major depressive disorder, bipolar I disorder, post-traumatic stress disorder, addiction, anhedonia or motivation-related aspects of schizophrenia (e.g. negative and cognitive symptoms), as well as Parkinson’s disease (e.g
• the psychiatric and neurological conditions featuring depressive, anhedonia, motivational and/or cognitive impairment symptoms include major depressive disorder, bipolar depression (such as bipolar I disorder), post-traumatic stress disorder (PTSD), addiction, schizophrenia (e.g., negative symptoms) and Parkinson’s disease (e.g. non-motor features such as depression, apathy and cognitive impairment).
• these different depression-related symptoms or areas of dysfunction co-occur and may be functionally related.
• a patient with major depression may report depressed mood, anhedonia, lack of motivation and cognitive difficulties.
• the same symptoms may be reported by patients diagnosed with other conditions in which similar impairments may co-occur, such as bipolar depression, post-traumatic stress disorder or addiction.
• schizophrenia is often thought of with respect to prominent hallucinations and delusions
• the depression-like negative symptoms and related cognitive symptoms are often the greater source of long-term disability and functional impairment.
• Parkinson’s disease involves prominent motor dysfunction, it also frequently has highly disabling non-motor features such as depression, apathy and cognitive impairment.
• a treatment approach that encompasses these multiple and related functional systems would be both of importance to any one of these clinical conditions, and equally may be applicable across them.
• cAMP cyclic adenosine monophosphate
• One embodiment of the present invention is a pharmaceutical composition (e.g., an oral composition such as an oral tablet or oral solution) comprising a PDE4 inhibitor (such as roflumilast, its N-oxide, or a pharmaceutically acceptable salt thereof) and at least one of a 5-HT4 agonist, an H3 antagonist or inverse agonist, a nicotinic a? receptor agonist, a fh adrenergic agonist or a TAAR1 agonist.
• a pharmaceutical composition e.g., an oral composition such as an oral tablet or oral solution
• a PDE4 inhibitor such as roflumilast, its N-oxide, or a pharmaceutically acceptable salt thereof
• the composition may comprise (a) a PDE4 inhibitor and (b) a 5-HT4 agonist.
• the composition comprises (a) roflumilast, its N-oxide, or a pharmaceutically acceptable salt thereof and (b) prucalopride or a pharmaceutically acceptable salt thereof (such as prucalopride succinate).
• the composition may comprise (a) from about 100 to about 500 mcg of roflumilast or the equivalent amount of a pharmaceutically acceptable salt of roflumilast and (b) from about 0.25 to about 4 mg of prucalopride or the equivalent amount of a pharmaceutically acceptable salt of prucalopride (such as prucalopride succinate).
• the composition comprises (a) roflumilast, its N-oxide, or a pharmaceutically acceptable salt thereof and (b) capeserod or a pharmaceutically acceptable salt thereof (such as capeserod hydrochloride).
• the composition may comprise (a) from about 100 to about 500 mcg of roflumilast or the equivalent amount of a pharmaceutically acceptable salt of roflumilast and (b) from about 1 pg to about 10 mg of capeserod or the equivalent amount of a pharmaceutically acceptable salt of capeserod (such as capeserod hydrochloride).
• the composition comprises (a) a PDE4 inhibitor and (b) an Eh antagonist or inverse agonist.
• the composition comprises (a) roflumilast, its N-oxide, or a pharmaceutically acceptable salt thereof and (b) pitolisant or a pharmaceutically acceptable salt thereof (such as pitolisant hydrochloride).
• the composition may comprise (a) from about 100 to about 500 mcg of roflumilast or the equivalent amount of a pharmaceutically acceptable salt of roflumilast and (b) an amount of pitolisant or a pharmaceutically acceptable salt thereof (such as pitolisant hydrochloride) equivalent to about 2 to about 40 mg of pitolisant hydrochloride.
• the composition comprises (a) roflumilast, its N-oxide, or a pharmaceutically acceptable salt thereof and (b) irdabisant or a pharmaceutically acceptable salt thereof (such as irdabisant hydrochloride).
• the composition may comprise (a) from about 100 to about 500 mcg of roflumilast or the equivalent amount of a pharmaceutically acceptable salt of roflumilast and (b) an amount of irdabisant or a pharmaceutically acceptable salt thereof (such as irdabisant hydrochloride) equivalent to about 1 to about 500 pg of irdabisant hydrochloride.
• the composition comprises (a) a PDE4 inhibitor and (b) a nicotinic a? receptor agonist.
• the composition comprises (a) roflumilast, its N-oxide, or a pharmaceutically acceptable salt thereof and (b) varenicline or a pharmaceutically acceptable salt thereof.
• the composition may comprise (a) from about 100 to about 500 mcg of roflumilast or the equivalent amount of a pharmaceutically acceptable salt of roflumilast and (b) from about 0.25 to about 3 mg of varenicline or the equivalent amount of a pharmaceutically acceptable salt thereof (such as varenicline tartrate).
• the composition comprises (a) a PDE4 inhibitor and (b) a [33 adrenergic agonist.
• the composition comprises (a) roflumilast, its N-oxide, or a pharmaceutically acceptable salt thereof and (b) amibegron or a pharmaceutically acceptable salt thereof.
• the composition may comprise (a) from about 100 to about 500 mcg of roflumilast or the equivalent amount of a pharmaceutically acceptable salt of roflumilast and (b) from about 100 to about 1400 mg of amibegron or the equivalent amount of a pharmaceutically acceptable salt thereof (e.g., amibegron hydrochloride).
• the composition comprises (a) a PDE4 inhibitor and (b) a TAAR1 agonist.
• the composition comprises (a) roflumilast, its N-oxide, or a pharmaceutically acceptable salt thereof and (b) ulotaront (SEP- 363856) or a pharmaceutically acceptable salt thereof.
• the composition may comprise (a) from about 100 to about 500 mcg of roflumilast or the equivalent amount of a pharmaceutically acceptable salt of roflumilast and (b) from about 5 to about 200 mg of ulotaront (SEP-363856) or the equivalent amount of a pharmaceutically acceptable salt thereof.
• the composition comprises (a) roflumilast, its N-oxide, or a pharmaceutically acceptable salt thereof and (b) ralmitaront (RO6889450) or a pharmaceutically acceptable salt thereof.
• the composition comprises (a) from about 100 to about 500 mcg of roflumilast or the equivalent amount of a pharmaceutically acceptable salt of roflumilast and (b) from about 5 to about 300 mg of ralmitaront (RO6889450) or the equivalent amount of a pharmaceutically acceptable salt thereof.
• the pharmaceutical composition may include a sub-emetic amount of component (a) (the PDE4 inhibitor).
• the pharmaceutical composition may include a sub-emetic amount of component (a) and an effective amount of components (a) and (b) together to treat the intended disorder, such as (a) depression (such as major depressive disorder or bipolar I disorder), (b) a psychiatric or neurological disorder in which anhedonia, motivation-related or cognition-related dysfunction exists, or (c) one or more symptoms associated with depression, anhedonia, or motivation-related or cognition-related impairments.
• depression such as major depressive disorder or bipolar I disorder
• a psychiatric or neurological disorder in which anhedonia, motivation-related or cognition-related dysfunction exists or one or more symptoms associated with depression, anhedonia, or motivation-related or cognition-related impairments.
• the pharmaceutical composition may include an effective amount of the recited components (such as components (a) and (b)) to increase cAMP signaling.
• Another embodiment is a method of treating (a) depression (such as major depressive disorder or bipolar I disorder), (b) a psychiatric or neurological disorder in which anhedonia, motivation-related or cognition-related dysfunction exists, or (c) one or more symptoms associated with depression, anhedonia, or motivation-related or cognition-related impairments in a subject in need thereof comprising administering to the subject an effective amount of a pharmaceutical composition of the present invention.
• an effective amount of the pharmaceutical composition is administered to increase cAMP signaling.
• the psychiatric or neurological disorder can be post-traumatic stress disorder (PTSD), schizophrenia, addiction, or Parkinson’s disease.
• Yet another embodiment is a method of treating (a) depression (such as major depressive disorder or bipolar I disorder), (b) a psychiatric or neurological disorder in which anhedonia, motivation-related or cognition-related dysfunction exists, or (c) one or more symptoms associated with depression, anhedonia, or motivation-related or cognition-related impairments in a subject in need thereof comprising administering to the subject an effective amount of a PDE4 inhibitor (such as roflumilast, its N-oxide, or a pharmaceutically acceptable salt thereof) and at least one of a 5-HT4 agonist, an Ek antagonist or inverse agonist, a nicotinic a? receptor agonist, a
• the psychiatric or neurological disorder can be post-traumatic stress disorder (PTSD), schizophrenia, addiction, or Parkinson’s disease.
• the method comprises administering an effective amount of (a) a PDE4 inhibitor and (b) a 5-HT4 agonist.
• the method comprises administering an effective amount of (a) roflumilast, its N-oxide, or a pharmaceutically acceptable salt thereof and (b) prucalopride or a pharmaceutically acceptable salt thereof (such as prucalopride succinate).
• the method may comprise administering (a) from about 100 to about 500 mcg per day of roflumilast or the equivalent amount of a pharmaceutically acceptable salt of roflumilast and (b) from about 0.25 to about 4 mg per day of prucalopride or the equivalent amount of a pharmaceutically acceptable salt of prucalopride (such as prucalopride succinate).
• the method comprises administering an effective amount of (a) roflumilast, its N-oxide, or a pharmaceutically acceptable salt thereof and (b) capeserod or a pharmaceutically acceptable salt thereof (such as capeserod hydrochloride).
• the method may comprise administering (a) from about 100 to about 500 mcg per day of roflumilast or the equivalent amount of a pharmaceutically acceptable salt of roflumilast and (b) from about Ipg to lOmg of per day of capeserod or the equivalent amount of a pharmaceutically acceptable salt of capeserod (such as capeserod hydrochloride).
• the method comprises administering an effective amount of (a) a PDE4 inhibitor and (b) an Eb antagonist or inverse agonist.
• the composition comprises administering an effective amount of (a) roflumilast, its N-oxide, or a pharmaceutically acceptable salt thereof and (b) pitolisant or a pharmaceutically acceptable salt thereof (such as pitolisant hydrochloride).
• the method may comprise administering (a) from about 100 to about 500 mcg per day of roflumilast or the equivalent amount of a pharmaceutically acceptable salt of roflumilast and (b) an amount of pitolisant or a pharmaceutically acceptable salt thereof (such as pitolisant hydrochloride) equivalent to about 2 to about 40 mg of pitolisant hydrochloride per day.
• the composition comprises administering an effective amount of (a) roflumilast, its N-oxide, or a pharmaceutically acceptable salt thereof and (b) irdabisant or a pharmaceutically acceptable salt thereof (such as irdabisant hydrochloride).
• the method may comprise administering (a) from about 100 to about 500 mcg per day of roflumilast or the equivalent amount of a pharmaceutically acceptable salt of roflumilast and (b) an amount of irdabisant or a pharmaceutically acceptable salt thereof (such as irdabisant hydrochloride) equivalent to about Ipg to about 500 pg of irdabisant hydrochloride per day.
• the method comprises administering an effective amount of (a) a PDE4 inhibitor and (b) a nicotinic a? receptor agonist.
• the composition comprises administering an effective amount of (a) roflumilast, its N-oxide, or a pharmaceutically acceptable salt thereof and (b) varenicline or a pharmaceutically acceptable salt thereof (such as varenicline tartrate).
• the method may comprise administering (a) from about 100 to about 500 mcg per day of roflumilast or the equivalent amount of a pharmaceutically acceptable salt of roflumilast and (b) from about 0.25 to about 3 mg per day of varenicline or the equivalent amount of a pharmaceutically acceptable salt of varenicline (such as varenicline tartrate).
• the method comprises administering an effective amount of (a) a PDE4 inhibitor and (b) a
• the composition comprises administering an effective amount of (a) roflumilast, its N-oxide, or a pharmaceutically acceptable salt thereof and (b) amibegron or a pharmaceutically acceptable salt thereof (e.g., amibegron hydrochloride).
• the method may comprise administering (a) from about 100 to about 500 mcg per day of roflumilast or the equivalent amount of a pharmaceutically acceptable salt of roflumilast and (b) from about 100 to about 1400 mg per day of amibegron or the equivalent amount of a pharmaceutically acceptable salt thereof (e.g., amibegron hydrochloride).
• the method comprises administering an effective amount of (a) a PDE4 inhibitor and (b) a TAAR-1 agonist.
• the composition comprises administering an effective amount of (a) roflumilast, its N-oxide, or a pharmaceutically acceptable salt thereof and (b) ulotaront (SEP-363856)or a pharmaceutically acceptable salt thereof.
• the method may comprise administering (a) from about 100 to about 500 mcg per day of roflumilast or the equivalent amount of a pharmaceutically acceptable salt of roflumilast and (b) from about 5 to about 200 mg per day of ulotaront (SEP-363856) or the equivalent amount of a pharmaceutically acceptable salt thereof.
• the composition comprises administering an effective amount of (a) roflumilast, its N-oxide, or a pharmaceutically acceptable salt thereof and (b) ralmitaront (RO6889450) or a pharmaceutically acceptable salt thereof.
• the method may comprise administering (a) from about 100 to about 500 mcg per day of roflumilast or the equivalent amount of a pharmaceutically acceptable salt of roflumilast and (b) from about 5 to about 300 mg per day of ralmitaront (RO6889450) or the equivalent amount of a pharmaceutically acceptable salt thereof.
• the methods described herein may include administering an effective amount of the recited components (such as components (a) and (b)) to increase cAMP signaling.
• a preferred PDE4 inhibitor in any of the compositions or methods described herein is roflumilast, AVE8112 (4-(cyclopropylmethoxy)-N-(3,5-dichloro-l- oxidopyridin-4-yl)-5-methoxypyridine-2-carboxamide), MEM1414, MEM1917, apremilast, cilomilast, crisaborole, ibudilast, luteolin, mesembrenon, piclamilast, rolipram, chlorbipram, GSK-256066, E-6005, MK-0873, BPN14770, HT-0712, or a pharmaceutically acceptable salt thereof.
• Other suitable PDE4 inhibitors include those disclosed in International Publication Nos. WO 95/04545 and WO 2008/145840, which are hereby incorporated by reference.
• a preferred 5-HT4 agonist in any of the compositions or methods described herein is prucalopride, cisapride, BIMU-8, CJ-033466, ML-10302, mosapride, renzapride, RS-67506, RS67333, SL65.0155 (capeserod), tegaserod, zacopride, metoclopramide, supride, or a pharmaceutically acceptable salt thereof (such as prucalopride succinate).
• a preferred EE antagonist or EE inverse agonist in any of the compositions or methods described herein is pitolisant, ABT-28, BF2.649, CEP-2640 l(irdabisant), GSK- 189254, GSK-239512, MK-0249, PF-3654746, or a pharmaceutically acceptable salt thereof (such as pitolisant hydrochloride).
• a preferred nicotinic a? receptor agonist for the compositions and methods described herein is varenicline, tilorone, A-582941, AR-R17779, TC-1698, bradanicline, encenicline, GTS-21, PHA-543613, PNU-292987, PHA-709829, SSR-180711, tropisetron, WAY-317538, anabasine, epiboxidine, PNU-120596, NS-1738, AVL-3288, A867744, ivermectine, BNC210 or a pharmaceutically acceptable salt thereof (such as varenicline tartrate).
• a preferred TAAR1 agonist for the compositions and methods described herein is ulotaront (SEP-363856), ralmitaront (RO6889450), RO5166017, RO5256390, RO5203648, RO5263397, tyramine, amphetamine, methamphetamine, 3, 4-methylenedi oxymethamphetamine (MDMA), or a pharmaceutically acceptable salt thereof.
• SEP-363856 ralmitaront
• RO6889450 RO5166017, RO5256390, RO5203648, RO5263397
• tyramine amphetamine
• methamphetamine methamphetamine
• MDMA 4-methylenedi oxymethamphetamine
• Figure 1 includes a schematic of (A) desired complementary exposure for the drug combinations, compared to (B) drug targets that do not overlap the disease module or (C) drug targets that overlap the disease module and each other.
• Complementary exposure means that each drug module is proximal to different parts of the disease module (and by extension, the drug modules do not overlap each other).
• Figure 2 is a table (Table 1) showing the distance and proximity of the specified drugs to certain diseases and cognition modules.
• the modules targeted by drugs within the combinations are significantly closer to the disease and cognition modules than randomly selected, similarly sized modules.
• Table 1 For all drugs, except the [33 adrenergic agonist, a network consisting of direct targets plus additional genes whose expression is perturbed upon treatment of neurons or neural precursor cells with the drug was used.
• the [33 adrenergic agonist direct targets only were used due to lack of gene expression data.
• negative Z-scores represent statistically significant results, as assessed by permutation tests.
• Figure 3 is a table (Table 2) showing that modules targeted by the drugs within the combinations are complementary to each other, within disease and cognition modules.
• PDE4 inhibitor + [33 adrenergic agonist a network consisting of direct targets plus additional genes whose expression is perturbed upon treatment of neurons or neural precursor cells with the drug was used.
• PDE4 inhibitor + [33 adrenergic agonist combination direct targets only were used due to lack of gene expression data. A positive separation value indicates the two drug modules are significantly distant from each other.
• Figure 4 is a table (Table 3) showing the distance and proximity of the specified drugs to certain diseases and cognition modules. Predicted gene expression modules targeted by the drug combinations are significantly closer to the disease modules than randomly selected, similarly sized modules, supporting their indication in treating the corresponding conditions. Prediction of gene expression networks for a PDE4 inhibitor + [33 adrenergic agonist combination was not done due to lack of data. In this table, negative Z-scores represent statistically significant results, as assessed by permutation tests. [0035]
• Figure 5 is a table (Table 4) which is a summary of the evidence for the drug combinations. All combinations are indicated for either all or the majority of the conditions as assessed by the two methodologies. For the PDE4 inhibitor + [33 adrenergic agonist combination, there is no available gene expression data. Therefore, no assessment of this indication was performed with the perturbation network methodology.
• the inventors theorize that a solution to this challenge is through combining a sub-emetic amount of a PDE4 inhibitor with a drug that has an additive or synergistic action with respect to increasing cAMP signaling.
• the goal of the drug combination is to result in an additive or greater effect through directly increasing cAMP levels while simultaneously having the PDE4 inhibitor prevent the breakdown of the cAMP that is induced.
• PDE4 inhibitors are effective antidepressants in humans, or that combination with any other drug increases the antidepressant effect over a PDE4 alone. As such, there is a high degree of uncertainty regarding whether a drug when administered in combination with a PDE4 can effectively treat depression.
• the net increase in cells targeted by the two drugs would be larger than that possible with either drug alone and at lower doses, thereby resulting in fewer side effects, side effects of reduced severity, or both.
• Second, in particular, use of a sub-emetic amount of the PDE4 inhibitor would ensure greater tolerability of the combination relative to the higher dose of a PDE4 inhibitor that would be otherwise required to reach the same level of cAMP increase.
• 5-HT4 agonist and PDE4 inhibitor combination One receptor whose activation results in an increase in cAMP levels is the serotonin 5-HT4 receptor. Activation of the 5-HT4 receptor with an agonist (such as a partial agonist) has resulted in antidepressant-like effects in animals (17), suggesting effects on the brain, though no 5-HT4 agonist has been developed for the treatment of neuropsychiatric conditions.
• 5-HT4 receptors Because of the prevalence of 5-HT4 receptors in the alimentary and urinary tracts, however, agonists for this receptor have been approved for indications such as irritable bowel syndrome, and constipation. In experiments with human or pig intestinal preparations, it has also been found that a combination of a PDE4 inhibitor and a 5-HT4 agonist can result in synergistic or additive activation of neuromuscular neurons (18, 19). Moreover, brain-penetrant oral 5-HT4 agonists have been reported (20).
• 5-HT4 agonists such as prucalopride
• prucalopride is indicated for the treatment of constipation
• the surprising combination of a 5-HT4 agonist and a sub-emetic amount of a PDE4 inhibitor can be used to treat symptoms related to depression, anhedonia, motivation-related or cognitive impairments.
• prucalopride or a pharmaceutically acceptable salt thereof such as prucalopride succinate
• Ipg -lOmg of the 5HT4 agonist capeserod (SL65.0155) or a pharmaceutically acceptable salt thereof such as capeserod hydrochloride
• 100-500mcg such as 100-400 mcg, 100-300 mcg, 100-250 mcg or 100-200 mcg
• roflumilast or an equivalent amount of a pharmaceutically acceptable salt of roflumilast is one such combination.
• This combination can both lead to greater improvement in depressive, anhedonia, motivational or cognitive symptoms and/or lead to lower side effects compared to use of a PDE4 inhibitor such as roflumilast alone.
• EE antagonist or inverse agonist and PDE4 inhibitor combination In addition to 5-HT4, the histamine EE receptor is also coupled to cAMP, though in this case its activation inhibits cAMP production via coupling to Gi proteins. As such, a drug that is an EE antagonist or inverse agonist would be expected to result in increased cAMP levels.
• EE antagonist or inverse agonist drugs have been tested for a number of cognitive disorders such as Alzheimer’s disease, dementia, schizophrenia, multiple sclerosis and attention-deficit hyperactivity disorder, as well as states of altered alertness such as narcolepsy and obstructive sleep apnea (21-23). No such drugs, however, have been used to treat depressive symptoms.
• combination drugs including an H3 antagonist or inverse agonist have not been tested for the treatment of the cognitive and alertness disorders listed above.
• One embodiment of the invention is a combination of an H3 antagonist or inverse agonist with a sub-emetic amount of a PDE4 inhibitor for treatment of symptoms related to depression, anhedonia, motivation-related or cognitive impairments.
• An example of an H3 antagonist or inverse agonist is pitolisant, which is approved for the treatment of narcolepsy.
• pitolisant hydrochloride or an equivalent amount of pitolisant or a different pharmaceutically acceptable salt thereof, or l-500pg of irdabisant (CEP-26401) or a pharmaceutically acceptable salt thereof (such as irdabisant hydrochloride), concurrently with 100-500mcg of the PDE4 inhibitor roflumilast or an equivalent amount of a pharmaceutically acceptable salt of roflumilast is one such combination.
• This combination can both lead to greater improvement in depressive, anhedonia, motivational or cognitive symptoms and/or lead to lower side effects compared to use of a PDE4 inhibitor such as roflumilast alone.
• Nicotinic a? receptor agonist and PDE4 inhibitor combination Without being bound by a particular theory, the inventors hypothesized that a drug which agonizes the nicotinic a7 receptor when combined with a PDE4 inhibitor can result in an additive or synergistic increase in cAMP levels. It has been recently reported that activation of the nicotinic a? receptor in the hippocampus results in an increase in cAMP levels by virtue of secondary effects on adenylyl cyclase, which produces cAMP (24). No nicotinic a? receptor agonist, however, has been used for the treatment of depression, one example of which is varenicline, which is approved for smoking cessation.
• varenicline has been approved in humans for smoking cessation, and initially carried a black box for increased risk for development of depression, a seemingly opposite outcome to our goal.
• One embodiment of the invention is a combination of a nicotinic a? receptor agonist with a sub-emetic amount of a PDE4 inhibitor for treatment of symptoms related to depression, anhedonia, motivation-related or cognitive impairments.
• a pharmaceutically acceptable salt of varenicline such as varenicline tartrate
• roflumilast concurrently with 100-500 mcg of the PDE4 inhibitor roflumilast or an equivalent amount of a pharmaceutically acceptable salt of roflumilast is one such combination.
• This combination can both lead to greater improvement in depressive, anhedonia, motivational or cognitive symptoms and/or lead to lower side effects compared to use of a PDE4 inhibitor such as roflumilast alone.
• fe adrenergic agonist and PDE4 inhibitor combination The [33 adrenergic receptor is another G-protein coupled receptor present in the brain, whose activation results in increased cAMP signaling. Most [ 3 agonists are not brain-penetrant, and thus have been used for peripheral adrenergic stimulation, such as is the case for mirabegron which is approved for overactive bladder. Though another [33 agonist, amibegron, is brain penetrant and had promising antidepressant-like effects in animals (25), it failed to show efficacy in two acute treatment clinical trials (as required by the U.S.
• One embodiment of the invention is a combination of an [33 agonist with a sub-emetic amount of a PDE4 inhibitor for treatment of symptoms related to depression, anhedonia, motivation-related or cognitive impairments.
• an [33 agonist is amibegron.
• 100-1400mg of amibegron, or an equivalent amount of a pharmaceutically acceptable salt thereof (e.g., amibegron hydrochloride) concurrently with 100- 500mcg of the PDE4 inhibitor roflumilast or an equivalent amount of a pharmaceutically acceptable salt of roflumilast is one such combination.
• This combination can both lead to greater improvement in depressive, anhedonia, motivational or cognitive symptoms and/or lead to lower side effects compared to use of a PDE4 inhibitor such as roflumilast alone.
• TAAR1 agonist and PDE4 inhibitor combination The trace amine- associated receptor 1 (TAAR1) is another G-protein coupled receptor present in the brain, whose activation results in increased cAMP signaling. Unlike the receptors above, it is located intracellularly and not on the cell surface. To date, no drug has been approved for any indication that specifically targets TAAR1 and activates it. One such TAAR1 agonist has shown initial promise in schizophrenia (26), but no TAAR1 agonist has been studied for efficacy in treating depression. Thus, a combination of a PDE4 inhibitor with a TAAR1 agonist is an unexpected combination for yielding an effective antidepressant.
• One embodiment of the invention is a combination of a TAAR1 agonist with a sub-emetic amount of a PDE4 inhibitor for the treatment of symptoms related to depression, anhedonia, motivation-related or cognitive impairments.
• An example of a TAAR1 agonist is ulotaront (SEP-363856).
• Another example is ralmitaront (RO6889450).
• 5-200mg of ulotaront (SEP-363856), or an equivalent amount of a pharmaceutically equivalent salt thereof, concurrently with 100-500mcg of the PDE4 inhibitor roflumilast or an equivalent amount of a pharmaceutically acceptable salt of roflumilast is one such combination.
• 5-300mg of ralmitaront (RO6889450), or an equivalent amount of a pharmaceutically equivalent salt thereof, concurrently with 100-500mcg of the PDE4 inhibitor roflumilast or an equivalent amount of a pharmaceutically acceptable salt of roflumilast is one such combination.
• each single drug targets genes that impact the disease module (where a module consists of a subnetwork where the nodes are genes implicated in disease), but different drugs target separate disease topological neighborhoods or sets of genes (31).
• the proximity between the single-drug modules (where the modules consist of drug targets) and depression, cognition, PTSD, schizophrenia, addiction, Parkinson’s disease, and bipolar disorder modules, as well as their separation from each other was evaluated.
• PPi brain-specific protein-protein interaction
• High-confidence disease-associated genes were identified based on mechanistic evidence from at least two published studies. All of the indications contain genes that are differentially expressed in post-mortem human brains. Additionally, for all indications except depression, genes from studies that were well supported with at least two lines of evidence were included. While one line of evidence could be genotype based (e.g. gene-based results from genome wide association studies), at least one line of evidence was also required to be functional evidence (e.g. expression quantitative trait loci, chromatin interaction studies, or gene expression studies in animal models). Finally, these gene lists were filtered to include only genes in the PPi network.
• the final sizes of the gene lists are as follows: 241 genes for depression (34-41), 470 genes for cognition (42-44), 26 genes for PTSD (45-55), 365 genes for schizophrenia (40, 56-64), 75 genes for addiction (55, 65-69), and 41 genes for Parkinson’s disease (70-81).
• DGIdb drug-gene interaction database (82)
• DGIdb drug-gene interaction database
• the resulting modules were filtered to include only genes whose expression is impacted by the drugs of interest. These genes were assessed by gene expression data (83).
• neural cell lines neural and neural precursor
• Genes whose expression levels respond to treatment are hypothesized to be impacted (directly or indirectly) by the drug.
• Drugs for which gene expression data is available were chosen, with the same drug mechanism of action (MO A) as in the combinations.
• gene expression data in response to rolipram was used to understand the effect of PDE4 inhibitors such as roflumilast, cisapride to understand the effect of 5-HT4 agonists such as prucalopride (both 5-HT4 agonists), ciproxifan to understand the effect of H3 inverse agonists such as pitolisant or irdabisant, amibegron to understand the effect of [33 adrenergic agonists and tyramine to understand the effect of TAAR1 agonists such as SEP-363856 (ulotaront) and ralmitaront (RO6889450).
• PDE4 inhibitors such as roflumilast
• cisapride to understand the effect of 5-HT4 agonists
• 5-HT4 agonists such as prucalopride (both 5-HT4 agonists)
• H3 inverse agonists such as pitolisant or irdabisant
• amibegron to understand
• the proximity of the drug module to the disease module is given by a Z-score of its distance relative to the generated distribution based on random modules, approximated by ⁇ (drug- disease)- (d (random-disease)) )/(c(d_( random -disease))) where (d_(random-disease)) is the average of the distance distribution and c(d_(random-disease)) the standard deviation.
• a Z-score ⁇ 0 indicates the drug module is significantly more proximal to the disease module than other gene sets in the network. Indeed, in these analyses, Z-scores remain stable and consistently negative or positive across multiple permutation shuffles, indicating statistical significance of the findings regarding the combinations.
• the proximities were computed with all the disease and cognition modules for each drug.
• combination expression ratio This information was used to predict how gene expression levels would change if exposed to two drugs at the same time, on a per-gene basis, in a metric called combination expression ratio.
• the computed single drug expression ratios for each gene were used. If the gene was downregulated upon treatment with each single drug, then the combination expression ratio was defined as the minimum value of the single drugs ratios. If the gene was upregulated in response to treatment of both drugs separately, the combination expression ratio was defined as the maximum value of the single drug ratios. If the ratios from each of the two drugs were in opposite directions, the combination expression ratio was computed as a sum of the single drug expression ratios (derived in Wu et al. 2010 (85)).
• a weight for each gene was then calculated by taking the absolute value of the logarithm of the computed expression ratios.
• a gene was considered as “perturbed” if its weight is greater or equal to 0.2, which is equivalent to a 20% single-drug- mediated up or downregulation of expression.
• the perturbed genes were mapped to the brain-specific PPi network previously constructed and the proximity of the combination modules to the depression, cognition, PTSD, schizophrenia, addiction, and Parkinson’s disease modules was evaluated. As shown in Table 3 ( Figure 4), the predicted combination networks are significantly proximal to multiple disease modules, supporting their indication in treating the corresponding conditions.
• PDE4 inhibitor refers to a compound that blocks or inhibits the activity of the phosphodiesterase 4 protein or any of its isoforms.
• Suitable PDE4 inhibitors antagonists include, but are not limited to, roflumilast, AVE8112, MEM1414, MEM1917, apremilast, cilomilast, crisaborole, ibudilast, luteolin, mesembrenon, piclamilast, rolipram, chlorbipram, GSK-256066, E-6005, MK-0873, BPN14770, HT-0712 and pharmaceutically acceptable salts thereof.
• 5-HT4 agonist refers to an agonist of the 5-HT4 receptor (including, but not limited to a 5-HT4 partial agonist), and includes but is not limited to prucalopride, cisapride, BIMU-8, CJ-033466, ML-10302, mosapride, renzapride, RS-67506, RS67333, SL65.0155 (capeserod), tegaserod, zacopride, metoclopramide, supride and pharmaceutically acceptable salts thereof (such as prucalopride succinate or capeserod hydrochloride).
• H3 antagonist or “H3 inverse agonist” refers to a compound that blocks activity at the H3 receptor.
• Suitable H3 antagonists or inverse agonists include, but are not limited to, pitolisant, ABT-28, BF2.649, CEP-26401 (irdabisant), GSK-189254, GSK-239512, MK-0249, PF-3654746 and pharmaceutically acceptable salts thereof (such as pitolisant hydrochloride or irdabisant hydrochloride).
• “Nicotinic a? receptor agonist” or “alpha7 receptor agonist” refers to an agonist (including, but not limited to, a partial agonist) of the nicotinic receptor containing an a? subunit. Suitable a?
• nicotinic receptor agonist include, but are not limited to, varenicline, tilorone, A-582941, AR-R17779, TC-1698, bradanicline, encenicline, GTS-21, PHA-543613, PNU-292987, PHA-709829, SSR-180711, tropisetron, WAY-317538, anabasine, epiboxidine, PNU-120596, NS-1738, AVL-3288, A867744, ivermectine, BNC210 or a pharmaceutically acceptable salt thereof (such as varenicline tartrate).
• 3 adrenergic agonist or “fh agonist” refers to an agonist of the [33 adrenergic receptor.
• Suitable [ 3 agonists include amibegron, mirabegron, vibegron, ritobegron, BRL37344, solabegron, or a pharmaceutically acceptable salt thereof.
• TAAR1 agonist refers to an agonist of the trace-amine associated receptor 1.
• Suitable TAAR1 agonists include ulotaront (SEP-363856), ralmitaront (RO6889450), RO5166017, RO5256390, RO5203648, RO5263397, tyramine, amphetamine, methamphetamine, and 3, 4-methylenedi oxy-methamphetamine (MDMA) or a pharmaceutically acceptable salt thereof.
• the term “about” in the context of a numerical value or range refers to ⁇ 10% of the numerical value or range recited.
• "effective" as in an amount effective to achieve an end means the quantity of a component that is sufficient to yield an indicated therapeutic response without undue adverse side effects (such as toxicity, irritation, or allergic response) commensurate with a reasonable benefit/risk ratio when used in the manner of this disclosure.
• the specific effective amount varies with such factors as the particular condition being treated, the physical condition of the patient, the type of mammal being treated, the duration of the treatment, the nature of concurrent therapy (if any), and the specific formulations employed and the structure of the compounds or its derivatives.
• to "treat” or “treating” encompasses, e.g., inducing inhibition, regression, or stasis of a disorder and/or disease, e.g. depression, or alleviating, lessening, suppressing, inhibiting, reducing the severity of, eliminating or substantially eliminating, or ameliorating a symptom of the disease or disorder.
• Diagnosis of various mental and psychological disorders, including depression may be found, e.g., in the Diagnostic and Statistical Manual of Mental Disorders (5 th Ed. DSM-5, American Psychiatric Association, 2013).
• Each active ingredient (such as a PDE4 inhibitor, 5-HT4 agonist, Ek antagonist or inverse agonist, a nicotinic a? receptor agonist, a
• a preferred route of administration is oral.
• the active ingredients may be administered in the form of a tablet, capsule, granules, or oral liquid.
• the methods and pharmaceutical compositions described herein may be used to treat (a) depression (such as major depressive disorder or bipolar I disorder), (b) a psychiatric or neurological disorder in which depressive, anhedonia, motivation-related or cognition-related dysfunction exists, or (c) one or more symptoms associated with depression, anhedonia, or motivation-related impairments.
• depression such as major depressive disorder or bipolar I disorder
• a psychiatric or neurological disorder in which depressive, anhedonia, motivation-related or cognition-related dysfunction exists or
• symptoms associated with depression, anhedonia, or motivation-related impairments include, but are not limited to, major depressive disorder, treatment resistant depression, residual depressive symptoms and dysthymia.
• Psychiatric or neurological disorders in which depressive, anhedonia, motivation-related or cognitive-related dysfunction exists include, but are not limited to, depression as part of bipolar I or bipolar II disorders, addiction (e.g., drug addiction), post-traumatic stress disorder, schizophrenia (in particular associated negative or cognitive symptoms) or Parkinson’s Disease (non-motor features such as depression, apathy or cognitive impairment).
• the method treats one or more non-motor features of Parkinson’s disease.
• Symptoms associated with depression which may be treated include, but are not limited to, depressed mood, blunted affect, anhedonia, alexithymia, and apathy.
• Motivation-related impairments which may be treated include, but are not limited to, inability to engage in previously rewarding experiences, reduced social interest or drive, inattentiveness to social inputs, reduced psychomotor activity, excessive sleep, avoidance of activities or social interactions, and decreased appetite.
• Cognitive impairment includes, but is not limited to, inability to focus on attentionally-demanding tasks, poor executive functioning, difficulties in inhibiting inappropriate response and deficits in memory formation or recall.
• the amount of the active ingredients to be administered is sufficient to increase cAMP molecular signaling in the brain.
• the amount of each component to be administered daily can be as shown in the table below.
• a sub-emetic amount of the PDE4 inhibitor is administered.
• an amount of the PDE4 inhibitor is administered which generally does not produce nausea or vomiting in the subject.
• an amount of the PDE4 inhibitor is administered which does not evoke vomiting in the subject.
• each active ingredient can be administered one or more times a day, daily, weekly, monthly or yearly.
• the pharmaceutical composition can include a sub-emetic amount of the PDE4 inhibitor.
• the composition includes an amount of the PDE4 inhibitor which when administered (e.g., orally administered) generally does not produce nausea or vomiting in the subject.
• the composition includes an amount of the PDE4 inhibitor which when administered (e.g., orally administered) does not evoke vomiting in the subject.
• the pharmaceutical composition includes an amount of the PDE4 inhibitor and the other active ingredient as recited in the table provided above for one day.
• the pharmaceutical composition includes an amount of the PDE4 inhibitor and the other active ingredient which when administered twice a day is equivalent to the total daily amount recited in the table provided above.
• the pharmaceutical composition can include one or more pharmaceutically acceptable excipients in addition to the active ingredients.
• the pharmaceutical composition may be suitable for any route of administration, such as nasal, rectal, intercisternal, buccal, intramuscular, intrasternal, intracutaneous, intrasynovial, intravenous, intraperitoneal, intraocular, periosteal, intra-articular injection, infusion, oral, topical, inhalation, parenteral, subcutaneous, implantable pump, continuous infusion, gene therapy, intranasal, intrathecal, intracerebroventricular, transdermal, or by spray, patch or injection.
• route of administration such as nasal, rectal, intercisternal, buccal, intramuscular, intrasternal, intracutaneous, intrasynovial, intravenous, intraperitoneal, intraocular, periosteal, intra-articular injection, infusion, oral, topical, inhalation, parenteral, subcutaneous, implantable pump, continuous infusion, gene therapy, intranasal, intrat
• the pharmaceutical composition may be formulated as a solid dosage form, such as capsules, pills, soft-gels, tablets, caplets, troches, wafer, sprinkle, or chewing for oral administration.
• the pharmaceutical composition may also be formulated as a liquid dosage form such as an elixir, suspension or syrup.
• the pharmaceutical composition may also be presented in a dosage form for transdermal application (e.g., a patch or an ointment) or oral administration.
• the pharmaceutical composition may be in a liquid dosage form or a suspension to be applied to nasal cavity or oral cavity using a dropper, a sprayer or a container.
• the pharmaceutical composition may be in a solid, salt or powder to be applied to nasal cavity or oral cavity using a sprayer, forced air or a container.
• the pharmaceutical acceptable excipient may be selected from pharmaceutically acceptable carriers, binders, diluents, adjuvants, or vehicles, such as preserving agents, fillers, polymers, disintegrating agents, glidants, wetting agents, emulsifying agents, suspending agents, sweetening agents, flavoring agents, perfuming agents, lubricating agents (such as magnesium stearate), acidifying agents, coloring agent, dyes, preservatives and dispensing agents.
• pharmaceutically acceptable excipients are described in the Handbook of Pharmaceutical Excipients, 6 th Ed., Pharmaceutical Press and American Pharmaceutical Association (2009).
• Pharmaceutically acceptable carriers are generally non-toxic to recipients at the dosages and concentrations employed and are compatible with other ingredients of the formulation.
• examples of pharmaceutically acceptable carriers include water, saline, dextrose solution, ethanol, polyols, vegetable oils, fats, ethyl oleate, liposomes, waxes polymers, including gel forming and non-gel forming polymers, and suitable mixtures thereof.
• the carrier may contain minor amounts of additives such as substances that enhance isotonicity and chemical stability.
• Such materials are non-toxic to recipients at the dosages and concentrations employed, and include buffers such as phosphate, citrate, succinate, acetic acid, and other organic acids or their salts; antioxidants such as ascorbic acid; low molecular weight (less than about ten residues) polypeptides, e.g., polyarginine or tripeptides; proteins, such as serum albumin, gelatin, or immunoglobulin; hydrophilic polymers such as polyvinylpyrrolidone; amino acids, such as glycine, glutamic acid, aspartic acid, or arginine; monosaccharides, disaccharides, and other carbohydrates including cellulose or its derivatives, glucose, mannose, or dextrins; chelating agents such as EDTA; sugar alcohols such as mannitol or sorbitol; counterions such as sodium; and/or nonionic surfactants such as polysorbates, poloxamers, or PEG.
• buffers such as phosphate, citrate
• binders include, but are not limited to, microcrystalline cellulose and cellulose derivatives, gum tragacanth, glucose solution, acacia mucilage, gelatin solution, molasses, polyvinylpyrrolidone, povidone, crospovidone, sucrose and starch paste.
• diluents include, but are not limited to, lactose, sucrose, starch, kaolin, salt, mannitol and dicalcium phosphate.
• excipients include, but are not limited to, starch, surfactants, lipophilic vehicles, hydrophobic vehicles, pregelatinized starch, microcrystalline cellulose, lactose, milk sugar, sodium citrate, calcium carbonate, and dicalcium phosphate.
• Typical excipients for dosage forms such as a soft-gel include gelatin for the capsule and oils such as soy oil, rice bran oil, canola oil, olive oil, com oil, and other similar oils; glycerol, polyethylene glycol liquids, and vitamin E TPGS as a surfactant.
• disintegrating agents include, but are not limited to, complex silicates, croscarmellose sodium, sodium starch glycolate, alginic acid, com starch, potato starch, bentonite, methylcellulose, agar and carboxymethylcellulose.
• glidants include, but are not limited to, colloidal silicon dioxide, talc, corn starch.
• wetting agents include, but are not limited to, propylene glycol monostearate, sorbitan monooleate, diethylene glycol monolaurate and polyoxyethylene 1 aural ether.
• lubricants include magnesium or calcium stearate, sodium lauryl sulphate, talc, starch, lycopodium and stearic acid as well as high molecular weight polyethylene glycols.
• Serotonin(4) (5-HT(4)) receptor agonists are putative antidepressants with a rapid onset of action. Neuron. 2007;55:712-725.

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