TREATMENT FOR PSORIASIS AND SKIN INFLAMMATORY DISEASES

Abstract

Present invention relates to development of prolyl hydroxylase inhibitor for treatment of Psoriasis and skin inflammatory diseases. Specifically, invention relates to development of compound of formula (Ia) for treatment of Psoriasis and skin inflammatory diseases. Invention also relates to pharmaceutical composition comprising compound of formula (Ia) for treatment of Psoriasis and skin inflammatory diseases.

Claims

1. Prolyl hydroxylase inhibitors for the treatment of Psoriasis and skin inflammatory diseases.

2. Prolyl hydroxylase inhibitors as claimed in claim 1 wherein Prolyl hydroxylase inhibitors are selected from Molidustat, Vadadustat and Daprodustat and compound of formula (Ia).

3. Pharmaceutical composition comprising prolyl hydroxylase inhibitors or pharmaceutically acceptable salts thereof and suitable pharmaceutically acceptable excipients for the treatment of Psoriasis and skin inflammatory diseases.

4. Pharmaceutical composition as claimed in claim 3 wherein prolyl hydroxylase inhibitors are selected from Molidustat, Vadadustat and Daprodustat and compound of formula (Ia).

5. Pharmaceutical composition comprising compound of formula (Ia) or its pharmaceutically acceptable salts and suitable pharmaceutically acceptable excipients for the treatment of Psoriasis and skin inflammatory diseases wherein compound of formula (Ia) is ##STR00004## .

6. Pharmaceutical composition as claimed in claim 5 wherein pharmaceutically acceptable salts are selected from calcium, sodium, potassium, lithium, barium, strontium, magnesium, cesium, copper, cobalt, iron, manganese, lead, aluminium, cadmium, silver, zinc, ammonium, methylamine, dimethylamine, ethylamine, diethyl amine, n-propyl amine, isopropyl amine, diisopropyl amine, N-methyl isopropyl amine, n-butyl amine, t-butyl amine, 2-butamine, 1,2-ethane diamine, N-methylglucamine, N,N,N-trimethyl ethanolamine hydroxide (choline), tromethamine, cyclohexylamine, N-methyl cyclohexylamine, guanidine, N-(4-aminobutyl) guanidine, dicyclohexylamine, benzene-methanamine, ethanolamine, diethanolamine, tris-(hydroxymethyl)methylamine, hydroxylamine, methanaminium, benzylamine, N-methylbenzylamine, N-ethyl benzylamine, 4-methoxybenzylamine, pyrrolidine, piperidine, piperazine, morpholine, 2-aminopyrimidine, alanine, lysine, arginine, histidine, threonine, proline, glutamine, glycine, 2-thiopheneethanamine, (2S)-3,3-dimethyl-2-butanamine, cyclopentanamine, cycloheptanamine, meglumine, benethamine, dibenzylamine, diphenylamine, α-naphthylamine, O-phenylenediamine, 1,3-Diaminopropane, (S)-α-naphthylethylamine, (S)-3-methoxyphenylethylamine, (S)-4-methoxyphenylethylamine, (S)-4-chlorophenylethylamine, (S)-4-methylphenylethylamine, cinchonine, cinchonidine, (-)-quinine, triethanolamine, imidazole, ethylenediamine, epolamine, morpholine 4-(2-hydroxyethyl), N-N-diethylethanolamine, deanol, hydrabamine, betaine, adamantanamine, L-adamantanmethylamine, tritylamine, glucamine, N-methyl pyrrolidine, urea, procaine, metformin, hexane1-6-diamine, 2-(2-aminoethoxy)ethanamine, N-methylmorpholine, and N-ethylmorpholine.

7. Pharmaceutical composition as claimed in claim 5 wherein pharmaceutically acceptable excipients are selected from diluent, binders, disintegrating agents, lubricating agents, glidant agent, coating redimix, gelling agent, humectant, chelating agents, permeation enhancers, preservatives, antioxidants, solubilizing agents, acidifying/alkalizing agent, Emollient and Emulsifying agents.

8. Pharmaceutical composition as claimed in claim 7 wherein diluents are selected from maltitol, lactitol, microcrystalline cellulose, magnesium or calcium or sodium carbonate, lactose, lactose monohydrate, di-calcium phosphate, compressible sugars, di-basic calcium phosphate dihydrate, mannitol lactose anyhydrous, magnesium oxide, maltodextrin, maltose, pullulan, sodium alginate, sodium bicarbonate, calcium silicate, calcium sulphate, cell and tribasic calcium phosphate or suitable combinations thereof.

9. Pharmaceutical composition as claimed in claim 7 wherein disintegrating agents are selected from maize starch, sodium starch glycolate, croscarmellose sodium, crospovidone, microcrystalline cellulose, modified com starch, sodium carboxymethyl starch, povidone, pregelatinized starch, agar, carboxymethyl cellulose calcium or sodium, colloidal silicon dioxide, chitosan, docusate sodium, hydroxyl propyl cellulose, magnesium aluminium silicate, maltose, methyl cellulose, polacrilin potassium, and alginic acid or suitable combinations thereof.

10. Pharmaceutical composition as claimed in 7 wherein lubricating agents are selected from lubricants include magnesium stearate, stearic acid, silica, fats, zinc or sucrose or sodium or calcium stearate, castor oil, hydrogenated castor oil, . Polyethylene glycol and its derivatives, sodium stearyl fumarate, talc, or fatty acids including lauric acid, oleic acid, glyceryl behenate, glyceryl monostearate, and C.sub.1-C.sub.10 fatty acid or suitable combinations thereof.

11. Pharmaceutical composition as claimed in claim 7 wherein humectant is selected from glycerin, propylene glycol, Polyethylene glycol, sorbitol solution, 1,2,6 -hexanetriol and suitable mixtures thereof.

12. Pharmaceutical composition as claimed in claim 7 wherein gelling agents are selected from carbomer, Methyl cellulose, sodium carboxy methyl clellulose, Carrageenan, colloidal silicon dioxide, Guar gum, hydroxypropyl methyl cellulose, hydroxyl ethyl cellulose, hydroxy propyl cellulose, Gelatin, polyethyene oxide, alginic acid, sodium alginate, fumed silica, polyvinylpyrrolidone, polyvinyl alcohol and suitable mixtures thereof.

13. Pharmaceutical composition as claimed in claim 7 wherein emollient are selected from carnauba wax, cetyl alcohol, cetyl ester wax, hydrous lanolin, lanolin, lanolin alcohols, paraffin, petrolatum. polyethylene glycol, stearic acid, stearyl alcohol, white wax, yellow wax, liquid paraffin, liquid petrolatum, jojoba oil, sesame oil, rapeseed oil, purcellin oil, 2-ethylhexyl palmitate, 2-octyldodecyl stearate, 2-octyldodecyl erucate, isostearyl isostearate, 2-octyldodecyl benzoate, triglycerides of caprylic/capric acids, octyldodecanol, isohexadecane, capmul MCM and suitable mixtures thereof.

14. Pharmaceutical composition as claimed in claim 7 wherein alkalizing agents are selected from trimethylamine, triethylamine, pyridine, picoline, ethanolamine, diethanolamine, triethanolamine, meglumine, dicyclohexylamine, N,N′-dibenzylethylenediamine, arginine, lysine, ornithine, sodium bicarbonates, sodium hydroxide, potassium hydroxide and suitable mixtures thereof.

15. Pharmaceutical composition as claimed in claim 7 wherein binders are selected from hypromellose 3 Cps, carbomers selected from carbopol, gellan, gum Arabic, hydrogenated vegetable oil, polymethacrylates selected from Eudragit, xanthan, lactose and Zein combinations thereof; glidant agents are selected from colloidal silica, calcium silicate, magnesium silicate, silicon hydrogel, cornstarch, talc, combinations thereof.

16. Pharmaceutical composition as claimed in claim 7 wherein chelating agents are selected from EDTA, disodium EDTA, trisodium EDTA, EGTA, disodium EGTA, trisodium EGTA, citric acid, phosphoric acid, succinic acid, and suitable mixtures thereof; permeation enhancers are selected from polyethylene glycol, polyethylene glycol monolaurate, butanediol, dimethylsulfoxide, decylmethylsulfoxide, diethylene glycol monoethyl ether, lauric acid, oleic acid, valeric acid, isopropyl myristate, isopropyl palmitate, methyl propionate, and ethyl oleate, urea, dimethyl acetamide, dimethylformamide 2- pyrrolidone, ethanolamine, methyl-2 -pyrrolidone, diethanolamine, triethanolamine, terpenes, alkanones, salicylic acid, citric acid, succinic acid and suitable mixtures thereof; preservatives are selected from Methyl paraben, Propyl paraben, benzoic acid, imidurea, sorbic acid, potassium sorbate, benzalkonium chloride, phenyl mercuric acetate, chlorobutanol, phenoxyethanol, benzyl alcohol, chlorocresol, metacresol, cetrimonium chloride, benzethonium chloride, sodium edetate, boric acid, phenol and suitable mixtures thereof; antioxidants are selected from ascorbic acid, glutathione, lipoic acid, uric acid, carotenes, α-tocopherol, ubiquinol, butylated hydroxyanisole, butylated hydroxytoluene, sodium benzoate, sodium thiosulphate, sodium metabisulphite, propyl gallate, and tertiary-butylhydroquinone, Idebenone, Lycopene and suitable mixtures thereof; and solubilizing agents are selected from Dimethyl malonate, diethyl succinate, diethyl glutarate, diethyl adipate, dipropyl adipate, dibutyl sebacate, diisopropyl sebacate, diethyl pimelate, diethyl suberate, diethyl azelate, dibutyl adipate, dibutyl sebacate, methyl ethyl succinate, diethyl ethyl-isopropylmalonate, diethyl isosuccinate, benzyl alcohol, benzyl benzoate, cyclodextrin, glycerine monostearate, lecithin, butylene glycol, dibutyl phthalate, diethyl phthalate, dimethyl ether, diethyl ether, ethyl acetate, ethyl lactate, ethyl oleate, glycofurol, isopropyl alcohol, triacetin, triethanolamine, hexylene glycol, dimethyl sulfoxide (DMSO) and/or dimethyl isosorbide, propylene glycol, glycerin, Diethylene glycol monoethyl ether, dimethyl acetamide, polyethylene glycol, polysorbate 80, 60 & 20, purified water, ethanol and suitable mixture thereof.

17. Pharmaceutical composition as claimed in claim 3 wherein effective amount of compound of formula (Ia) is ranging from 1% to 10%w/w.

18. Pharmaceutical composition as claimed in claim 3 is administered orally, intravenously, parentally or topically.

19. Pharmaceutical composition as claimed in claim 5 further comprising additional therapeutic agents.

20. Pharmaceutical composition as claimed in claim 19 wherein additional therapeutic agents are selected from class of a PDE4 inhibitor, methotrexate or derivatives thereof, cyclosporine or derivatives thereof, vitamins D, E and A or derivatives thereof, glucocorticoid or derivatives thereof, anti-inflammatory agents, immunosuppressive agents, antihistamines, monoclonal antibodies and fusion proteins, cytokines and mediators, antibiotic or derivatives thereof, antifungal agents or derivatives thereof, hormones, peroxisome proliferator-activated receptor gamma activators or derivatives thereof, anti-viral agents or derivatives thereof, vegetable and/or animal extracts, phytochemicals or derivatives thereof, zinc pyrithione and/or other essential minerals, phototherapy and cell hyper proliferation modulators.

21. Compound of formula (Ia) or its pharmaceutically acceptable salts for the treatment of Psoriasis and skin inflammatory diseases wherein compound of formula (Ia) is ##STR00005## .

22. Compound of formula (Ia) or its pharmaceutically acceptable salts as claimed in claim 12 wherein pharmaceutically acceptable salts are selected from calcium, sodium, potassium, lithium, barium, strontium, magnesium, cesium, copper, cobalt, iron, manganese, lead, aluminium, cadmium, silver, zinc, ammonium, methylamine, dimethylamine, ethylamine, diethyl amine, n-propyl amine, isopropyl amine, diisopropyl amine, N-methyl isopropyl amine, n-butyl amine, t-butyl amine, 2-butamine, 1,2-ethane diamine, N-methylglucamine, N,N,N-trimethyl ethanolamine hydroxide (choline), tromethamine, cyclohexylamine, N-methyl cyclohexylamine, guanidine, N-(4-aminobutyl) guanidine, dicyclohexylamine, benzene-methanamine, ethanolamine, diethanolamine, tris-(hydroxymethyl)methylamine, hydroxylamine, methanaminium, benzylamine, N-methylbenzylamine, N-ethyl benzylamine, 4-methoxybenzylamine, pyrrolidine, piperidine, piperazine, morpholine, 2-aminopyrimidine, alanine, lysine, arginine, histidine, threonine, proline, glutamine, glycine, 2-thiopheneethanamine, (2S)-3,3-dimethyl-2-butanamine, cyclopentanamine, cycloheptanamine, meglumine, benethamine, dibenzylamine, diphenylamine, α-naphthylamine, O-phenylenediamine, 1,3-Diaminopropane, (S)-α-naphthylethylamine, (S)-3-methoxyphenyl ethylamine, (S)-4-methoxyphenylethylamine, (N)-4-chlorophenylethylamine, (S)-4-methylphenylethylamine, cinchonine, cinchonidine, (-)-quinine, triethanolamine, imidazole, ethylenediamine, epolamine, morpholine 4-(2-hydroxyethyl), N-N-diethylethanolamine, deanol, hydrabamine, betaine, adamantanamine, L-adamantanmethylamine, tritylamine, glucamine, N-methyl pyrrolidine, urea, procaine, metformin, hexane1-6-diamine, 2-(2-aminoethoxy)ethanamine, N-methylmorpholine, and N-ethylmorpholine.

23. Method of treating Psoriasis and skin inflammatory diseases using compound of formula (Ia) or its pharmaceutically acceptable salts wherein compound of formula (Ia) is ##STR00006## .

Description

DESCRIPTION OF ACCOMPANYING FIGURES

[0014] FIG. 1. The effect of topical application of compound of formula (Ia) on IMQ-induced psoriasis-like skin lesions in mice.

[0015] FIG. 2. The effect of topical application of compound of formula (Ia) on ear thickness and skinfold thickness in IMQ-induced psoriasis in mice.

[0016] FIG. 3. The effect of topical application of compound of formula (Ia) on ear thickness in Mannan-induced psoriasis in mice.

DESCRIPTION OF THE INVENTION

[0017] The term ‘treating’ or ‘treatment’ or condition as used herein means: preventing or delaying the appearance of clinical symtomps of the state, disorder or condition developing in a mammal.

[0018] The term ‘preventing’ refers to barring a subject from acquiring a disorder or disease in the first place.

[0019] The term ‘pharmaceutically acceptable’ use embraces both human and veterinary use.

[0020] The present invention describes prolyl hydroxylase inhibitors suitable for the treatment of Psoriasis and skin inflammatory diseases.

[0021] Wherein prolyl hydroxylase inhibitors are selected from Roxadustat, Molidustat, Desidustat (compound of formula (Ia)) and Daprodustat.

[0022] In an embodiment is provided suitable pharmaceutical composition for the treatment of psoriasis and skin inflammatory diseases comprising the compound of Roxadustat, Molidustat and Daprodustat or its pharmaceutically acceptable salt along with suitable excipients as defined hereinafter.

[0023] In another embodiment, the present invention provides a method of treating a subject suffering from psoriasis and skin inflammatory diseases which comprises treatment of a patient in need of such therapy, with Roxadustat, Molidustat and Daprodustat or its pharmaceutically acceptable salt or suitable pharmaceutical compositions containing them.

[0024] In a further embodiment the present invention provides use of the Roxadustat, Molidustat and Daprodustat or its pharmaceutically acceptable salt or their suitable pharmaceutical compositions for the treatment of psoriasis and skin inflammatory diseases.

[0025] The effective amount of the Roxadustat, Molidustat and Daprodustat is selected from 1 mg to 500 mg preferably 1 mg to 250 mg and more preferably 4 mg to 50 mg.

[0026] In one embodiment the present invention disclose Roxadustat, Molidustat and Daprodustat or its pharmaceutically acceptable salt or suitable pharmaceutical compositions can also be used for the treatment of other skin inflammatory diseases such as: dermatomycosis, scleroderma, epidermolysis bullosa, eczema and systemic lupus erythematous affecting skin. It can also be used for the treatment of hives, acneiform eruptions, auto inflammatory diseases (Blau syndrome, Majeed syndrome, Muckle-Wells syndrome), chronic blistering diseases, skin mucus diseases, inflammation of skin appendages, diseases of alteration in pigmentation, drug-induced skin diseases, eosinophilic cutaneous conditions, bacterial or viral or fungal or parasite skin infections, lichen planus, lymphoid-related cutaneous conditions, monocyte-and macrophage-related cutaneous inflammation, reactive neutrophilic cutaneous condition, utricaria and other skin inflammation of unknown origin.

[0027] In an embodiment the present invention provides Roxadustat, Molidustat and Daprodustat or its pharmaceutically acceptable salts is administrated orally, intravenously, parentally or topically in the subject who is in need of treatment.

[0028] In yet another embodiment the present invention provides the administration of Roxadustat, Molidustat and Daprodustat and their pharmaceutically acceptable salts alone or in combination with other suitable agents as therapeutic agent for the treatment of Psoriasis and skin inflammatory diseases.

[0029] In an embodiment, the additional therapeutic agent used is selected from a PDE4 inhibitor, methotrexate or derivatives thereof, cyclosporine or derivatives thereof, vitamins D, E and A or derivatives thereof, glucocorticoid or derivatives thereof, anti-inflammatory agents, immunosuppressive agents, antihistamines, monoclonal antibodies and fusion proteins, cytokines and mediators, antibiotic or derivatives thereof, antifungal agents or derivatives thereof, hormones, peroxisome proliferator-activated receptor gamma activators or derivatives thereof, anti-viral agents or derivatives thereof, vegetable and/or animal extracts, phytochemicals or derivatives thereof, zinc pyrithione and/or other essential minerals, phototherapy and cell hyper proliferation modulators.

[0030] In a Preferred embodiment the present invention provides compound of formula (Ia) which is suitable for the treatment of Psoriasis and skin inflammatory diseases.

##STR00003##

[0031] In an embodiment is provided suitable pharmaceutical composition for the treatment of psoriasis and skin inflammatory diseases comprising the compound of formula (Ia) or its pharmaceutically acceptable salt along with suitable excipients as defined hereinafter.

[0032] In another embodiment, the present invention provides a method of treating a subject suffering from psoriasis and skin inflammatory diseases which comprises treatment of a patient in need of such therapy, with compound of formula (Ia) or its pharmaceutically acceptable salt or suitable pharmaceutical compositions containing them.

[0033] The pharmaceutical acceptable salts of the compound of formula (Ia) is inorganic metal salt or organic amines salts.

[0034] Wherein inorganic metal salt is selected from calcium, sodium, potassium, lithium, barium, strontium, magnesium, cesium, copper, cobalt, iron, manganese, lead, aluminium, cadmium, silver, zinc, ammonium and the like;

[0035] Wherein organic amines salt is selected from methylamine, dimethylamine, ethylamine, diethyl amine, n-propyl amine, isopropyl amine, diisopropyl amine, N-methyl isopropyl amine, n-butyl amine, t-butyl amine, 2-butamine, 1,2-ethane diamine, N-methylglucamine, N,N,N-trimethyl ethanolamine hydroxide (choline), tromethamine, cyclohexylamine, N-methyl cyclohexylamine, guanidine, N-(4-aminobutyl) guanidine, dicyclohexylamine, benzene-methanamine, ethanolamine, diethanolamine, tris-(hydroxymethyl)methylamine, hydroxylamine, methanaminium, benzylamine, N-methylbenzylamine, N-ethyl benzylamine, 4-methoxybenzylamine, pyrrolidine, piperidine, piperazine, morpholine, 2-aminopyrimidine, alanine, lysine, arginine, histidine, threonine, proline, glutamine, glycine, 2-thiopheneethanamine, (2S)-3,3-dimethyl-2-butanamine, cyclopentanamine, cycloheptanamine, meglumine, benethamine, dibenzylamine, diphenylamine, α-naphthylamine, O-phenylenediamine, 1,3-Diaminopropane, (S)-α-naphthylethylamine, (S)-3-methoxyphenylethylamine, (S)-4-methoxyphenylethylamine, (S)-4-chlorophenylethylamine, (S)-4-methylphenylethylamine, cinchonine, cinchonidine, (-)-quinine, triethanolamine, imidazole, ethylenediamine, epolamine, morpholine 4-(2-hydroxyethyl), N-N-diethylethanolamine, deanol, hydrabamine, betaine, adamantanamine, L-adamantanmethylamine, tritylamine, glucamine, N-methyl pyrrolidine, urea, procaine, metformin, hexane1-6-diamine, 2-(2-aminoethoxy)ethanamine, N-methylmorpholine, and N-ethylmorpholine.

[0036] In an embodiment, the effective amount of the said compound of formula (Ia) is selected from 25 mg to 250 mg preferably 50 mg to 150 mg.

[0037] In other preferred embodiment, the pharmaceutical composition comprising effective amount of compound of formula (Ia) is ranging from 1% to 10%w/w.

[0038] In one of the embodiment a compound of formula (Ia) or its pharmaceutically acceptable salt or suitable pharmaceutical compositions can also be used for the treatment of other skin inflammatory diseases such as: dermatomycosis, scleroderma, epidermolysis bullosa, eczema and systemic lupus erythematous affecting skin. It can also be used for the treatment of hives, acneiform eruptions, autoinflammatory diseases (Blau syndrome, Majeed syndrome, Muckle-Wells syndrome), chronic blistering diseases, skin mucus diseases, inflammation of skin appendages, diseases of alteration in pigmentation, drug-induced skin diseases, eosinophilic cutaneous conditions, bacterial or viral or fungal or parasite skin infections, lichen planus, lymphoid-related cutaneous conditions, monocyte-and macrophage-related cutaneous inflammation, reactive neutrophilic cutaneous condition, utricaria and other skin inflammation of unknown origin.

[0039] In an embodiment the present invention provides a compound of formula (Ia) or its pharmaceutically acceptable salts is administrated orally, intravenously, parentally or topically in the subject who is in need of treatment. In a preferred embodiment the present invention provides a compound of formula (Ia) or its pharmaceutically acceptable salt is to be administered orally or topically.

[0040] In yet another embodiment the present invention provides the administration of compound of formula (Ia) and their pharmaceutically acceptable salts alone or in combination with other suitable agents as therapeutic agent for the treatment of Psoriasis and skin inflammatory diseases.

[0041] In an embodiment, the additional therapeutic agent used is selected from a PDE4 inhibitor, methotrexate or derivatives thereof, cyclosporine or derivatives thereof, vitamins D, E and A or derivatives thereof, glucocorticoid or derivatives thereof, anti-inflammatory agents, immunosuppressive agents, antihistamines, monoclonal antibodies and fusion proteins, cytokines and mediators, antibiotic or derivatives thereof, antifungal agents or derivatives thereof, hormones, peroxisome proliferator-activated receptor gamma activators or derivatives thereof, anti-viral agents or derivatives thereof, vegetable and/or animal extracts, phytochemicals or derivatives thereof, zinc pyrithione and/or other essential minerals, phototherapy and cell hyper proliferation modulators.

[0042] In an embodiment the present invention also provides a suitable pharmaceutical composition of compounds of formula (Ia) or its pharmaceutically acceptable salts. The pharmaceutical composition of the present invention essentially comprises of: [0043] the pharmaceutically active substance of formula (Ia) its pharmaceutically acceptable salts; [0044] optionally with one or more pharmaceutically acceptable excipients.

[0045] The pharmaceutically acceptable excipients are selected at least one from diluent, binders, disintegrating agents, lubricating agents, glidant agent, coating redimix, gelling agent, humectant, chelating agents, permeation enhancers, preservatives, antioxidants, solubilizing agents, acidifying/alkalizing agent, Emollient, Emulsifying agents and the like

[0046] Diluents include, but are not limited to starch and its processed and co-processed derivertives, saccharides, di saccharides, sucrose, lactose, polysaccharides, cellulose, cellulose ethers, cellulose acetate, hydroxypropyl cellulose, sugar alcohols, xylitol, sorbitol, maltitol, lactitol, microcrystalline cellulose, magnesium or calcium or sodium carbonate, lactose, lactose monohydrate, di-calcium phosphate, compressible sugars, di-basic calcium phosphate dihydrate, mannitol lactose anyhydrous, magnesium oxide, maltodextrin, maltose, pullulan, sodium alginate, sodium bicarbonate, calcium silicate, calcium sulphate, cell and tribasic calcium phosphate or suitable combinations thereof and other such materials known to those of ordinary skill in the art.

[0047] Binders include, but are not limited to hypromellose 3 Cps, carbomers selected from carbopol, gellan, gum Arabic, hydrogenated vegetable oil, polymethacrylates selected from Eudragit, xanthan, lactose and Zein combinations thereof and other such materials known to those of ordinary skill in the art.

[0048] Disintegrating agents include, maize starch, sodium starch glycolate, croscarmellose sodium, crospovidone, microcrystalline cellulose, modified com starch, sodium carboxymethyl starch, povidone, pregelatinized starch, agar, carboxymethyl cellulose calcium or sodium, colloidal silicon dioxide, chitosan, docusate sodium, hydroxyl propyl cellulose, magnesium aluminium silicate, maltose, methyl cellulose, polacrilin potassium, and alginic acid or suitable combinations thereof and other such materials known to those of ordinary skill in the art.

[0049] Glidant agents include, but are not limited to, colloidal silica, calcium silicate, magnesium silicate, silicon hydrogel, cornstarch, talc, combinations thereof and other such materials known to those of ordinary skill in the art.

[0050] Lubricating agents include, but are not limited to, magnesium stearate, stearic acid, silica, fats, zinc or sucrose or sodium or calcium stearate, castor oil, hydrogenated castor oil, . Polyethylene glycol and its derivatives, sodium stearyl fumarate, talc, or fatty acids including lauric acid, oleic acid, glyceryl behenate, glyceryl monostearate, and C.sub.1-C.sub.10 fatty acid or suitable combinations thereof and other such materials known to those of ordinary skill in the art.

[0051] Coating redimix is selected from Opadry Pink all such materials known to those of ordinary skill in the art.

[0052] Solubilizers/co-solvents used anywhere in the description may be selected from Dimethyl malonate, diethyl succinate, diethyl glutarate, diethyl adipate, dipropyl adipate, dibutyl sebacate, diisopropyl sebacate, diethyl pimelate, diethyl suberate, diethyl azelate, dibutyl adipate, dibutyl sebacate, methyl ethyl succinate, diethyl ethyl-isopropylmalonate, diethyl isosuccinate, benzyl alcohol, benzyl benzoate, cyclodextrin, glycerine monostearate, lecithin, butylene glycol, dibutyl phthalate, diethyl phthalate, dimethyl ether, diethyl ether, ethyl acetate, ethyl lactate, ethyl oleate, glycofurol, isopropyl alcohol, triacetin, triethanolamine, hexylene glycol, dimethyl sulfoxide (DMSO) and/or dimethyl isosorbide, propylene glycol, glycerin, Diethylene glycol monoethyl ether, dimethyl acetamide, polyethylene glycol, polysorbate 80, 60 & 20, purified water, ethanol and suitable mixture thereof.

[0053] Permeation enhancers used anywhere in the description may be selected from polyethylene glycol, polyethylene glycol monolaurate, butanediol, dimethylsulfoxide, decylmethylsulfoxide, diethylene glycol monoethyl ether (e.g., Transcutol® P), lauric acid, oleic acid, valeric acid, isopropyl myristate, isopropyl palmitate, methyl propionate, and ethyl oleate; urea, dimethyl acetamide, dimethylformamide 2- pyrrolidone, ethanolamine, methyl-2 -pyrrolidone, diethanolamine, triethanolamine, terpenes, alkanones, salicylic acid, citric acid, succinic acid and suitable mixtures thereof.

[0054] Humectants used anywhere in the description may be selected from glycerin, propylene glycol, Polyethylene glycol, sorbitol solution, 1,2,6 -hexanetriol and suitable mixtures thereof.

[0055] Antioxidants used anywhere in the description may be selected from ascorbic acid (vitamin C), glutathione, lipoic acid, uric acid, carotenes, a-tocopherol (vitamin E), ubiquinol, butylated hydroxyanisole, butylated hydroxytoluene, sodium benzoate, sodium thiosulphate, sodium metabisulphite, propyl gallate (PG, E310), and tertiary-butylhydroquinone, Idebenone, Lycopene and suitable mixtures thereof.

[0056] Preservatives used anywhere in the description may be selected from Methyl paraben, Propyl paraben, benzoic acid, imidurea, sorbic acid, potassium sorbate, benzalkonium chloride, phenyl mercuric acetate, chlorobutanol, phenoxyethanol, benzyl alcohol, chlorocresol, metacresol, cetrimonium chloride, benzethonium chloride, sodium edetate, boric acid, phenol and suitable mixtures thereof.

[0057] Chelating agents used anywhere in the description may be selected from EDTA, disodium EDTA, trisodium EDTA, EGTA, disodium EGTA, trisodium EGTA, citric acid, phosphoric acid, succinic acid, and suitable mixtures thereof.

[0058] Acidifying/alkalizing agents used anywhere in the description may be selected from trimethylamine, triethylamine, pyridine, picoline, ethanolamine, diethanolamine, triethanolamine, meglumine, dicyclohexylamine, N,N′-dibenzylethylenediamine, arginine, lysine, ornithine, sodium bicarbonates, sodium hydroxide, potassium hydroxide and suitable mixtures thereof.

[0059] Buffers used anywhere in the description may be selected from citrate/citric acid buffers, acetate/acetic acid buffers, phosphate/phosphoric acid buffers, formate/formic acid buffers, propionate/propionic acid buffers, carbonate/carbonic acid buffers, ammonium/ammonia buffers and suitable mixtures thereof.

[0060] Gelling agents used anywhere in the description may be selected from carbomer, Methyl cellulose, sodium carboxy methyl clellulose, Carrageenan, colloidal silicon dioxide, Guar gum, hydroxypropyl methyl cellulose, hydroxyl ethyl cellulose, hydroxy propyl cellulose, Gelatin, polyethyene oxide, alginic acid, sodium alginate, fumed silica, polyvinylpyrrolidone, polyvinyl alcohol and suitable mixtures thereof.

[0061] Emollient/ stiffening agents used anywhere in the description may be selected from carnauba wax, cetyl alcohol, cetyl ester wax, hydrous lanolin, lanolin, lanolin alcohols, paraffin, petrolatum. polyethylene glycol, stearic acid, stearyl alcohol, white wax, yellow wax, liquid paraffin, liquid petrolatum, jojoba oil, sesame oil, rapeseed oil, purcellin oil, 2-ethylhexyl palmitate, 2-octyldodecyl stearate, 2-octyldodecyl erucate, isostearyl isostearate, 2-octyldodecyl benzoate, triglycerides of caprylic/capric acids, octyldodecanol, isohexadecane, capmul MCM and suitable mixtures thereof.

[0062] Emulsifying agents used anywhere in the description may be selected from polysorbate 20, polysorbate 60, polysorbate 80, poloxamer, emulsifying wax, sorbitan monostearate, sorbitan monooleate, sodium lauryl sulphate, propylene glycol monostearate, glyceryl monostearate and suitable mixtures thereof.

[0063] Ointment bases used anywhere in the description may be selected from oleaginous bases such as petrolatum, white/yellow petrolatum, liquid paraffin, hard paraffin, white ointment; absorption bases such as lanolin, anhydrous lanolin, cold cream, etc.; water removable bases: hydrophilic ointments, vanishing creams and water; water soluble bases such as polyethylene glycol 200, 300, 400, 1500, 3000, 6000 and suitable mixtures thereof.

[0064] The pharmaceutical composition comprising effective amount of the said compound of formula (Ia) is selected from 25 mg to 250 mg preferably 50 mg to 150 mg.

[0065] In one of the preferred embodiment, the present pharmaceutical composition comprising effective amount of compound of formula (Ia) is ranging from 0.1% to 25% w/w.

[0066] In one of the embodiment pharmaceutical compositions can also be used for the treatment of other skin inflammatory diseases such as: dermatomycosis, scleroderma, epidermolysis bullosa, eczema and systemic lupus erythematous affecting skin. It can also be used for the treatment of hives, acneiform eruptions, autoinflammatory diseases (Blau syndrome, Majeed syndrome, Muckle-Wells syndrome), chronic blistering diseases, skin mucus diseases, inflammation of skin appendages, diseases of alteration in pigmentation, drug-induced skin diseases, eosinophilic cutaneous conditions, bacterial or viral or fungal or parasite skin infections, lichen planus, lymphoid-related cutaneous conditions, monocyte-and macrophage-related cutaneous inflammation, reactive neutrophilic cutaneous condition, utricaria and other skin inflammation of unknown origin.

[0067] In an embodiment the present invention provides a pharmaceutical composition comprising compound of formula (Ia) or its pharmaceutically acceptable salts is administrated orally, intravenously, parentally or topically in the subject who is in need of treatment.

[0068] In a preferred embodiment the present invention provides a pharmaceutical composition comprising compound of formula (Ia) or its pharmaceutically acceptable salt is to be administered orally or topically.

[0069] In an embodiment the present invention provides the administration of pharmaceutical composition of compound of formula (Ia) further comprising additional therapeutic agents for the treatment of Psoriasis and skin inflammatory diseases.

[0070] In another embodiment, the additional therapeutic agent used in is selected from a PDE4 inhibitor, methotrexate or derivatives thereof, cyclosporine or derivatives thereof, vitamins D, E and A or derivatives thereof, glucocorticoid or derivatives thereof, anti-inflammatory agents, immunosuppressive agents, antihistamines, monoclonal antibodies and fusion proteins, cytokines and mediators, antibiotic or derivatives thereof, antifungal agents or derivatives thereof, hormones, peroxisome proliferator-activated receptor gamma activators or derivatives thereof, anti-viral agents or derivatives thereof, vegetable and/or animal extracts, phytochemicals or derivatives thereof, zinc pyrithione and/or other essential minerals, phototherapy and cell hyper proliferation modulators.

[0071] In yet another embodiment the present invention provides method of treating Psoriasis and skin inflammatory diseases using compound of formula (Ia) or its pharmaceutically acceptable salts.

[0072] The compound of formula (Ia) is known as Desidustat. The compound of formula (Ia), Roxadustat, Vadadustat and Daprodustat may be prepared by any of the methods known in the art including those processes disclosed in the prior art such as those mentioned elsewhere in the specification.

[0073] While the present invention has been described in terms of a few specific aspects, modifications and equivalents thereof, in light of teaching and disclosure of the present invention, which are apparent of the skilled artisan, are to be construed as included within the scope of the invention.

Example 1

[0074] The efficacy of the compound in the treatment of psoriasis is evaluated as follows:

Imiquimod-Induced Psoriasis

Study Design and Treatment

[0075] The 8 to 10 week old male C57 mice (18-20 g) received a daily topical dose of commercially available Imiquimod (IMQ) cream (5%, Imiquad;) on the shaved back and the right ear for 5 consecutive days, translating in a daily dose of 3.125 mg of the active compound to establish a model of IMQ-induced psoriasis. To examine the efficacy of topical solution of compound of formula (Ia), mice were randomly divided into 3 groups: IMQ-induced model group (IMQ) and IMQ + 5% compound of formula (Ia) solution and control group. Treatment was started on day 1 after the topical application of IMQ and continued upto day 5. All animals were assessed for the severity of the psoriasis-like skin condition, using 3 elements of the Psoriasis Area Severity Index (PASI), to assign a score of 0-4 (0, none; 1, mild; 2, moderate; 3, severe; 4, very severe) for each of the parameters erythema, scaling and thickness. The cumulative score (erythema plus scaling plus thickness) served to indicate the severity of inflammation (scale 0-12). Ear thickness was measured every day using thickness meter.

Results

Compound of Formula (Ia) Treatment Reduces IMQ-Induced Skin Inflammation and Ear Thickness in Mice

[0076] The psoriasis-like skin conditions became apparent from day 3 onwards in IMQ group (FIG. 1). Erythema score and skin thickness score started to appear from day 3 while scale score was apparent from day 4 of the IMQ treatment (FIGS. 1A-C). IMQ application increased PASI score from day onwards (FIG. 1D). Topical application of compound of formula (Ia) reduced erythema score 46.2 ± 7.7% erythema score by 63.6 ± 11.5% and skin thickness score by 26.3 ± 10.4% when compared with IMQ-control (FIGS. 1A-C). Compound of formula (Ia) decreased PASI score to 41.9 ± 7.6 % when compared with IMQ-control (FIG. 1D). Thickness of the right ears the IMQ group was increased to 0.40 mm from 0.21 mm (FIG. 2A). In the compound of formula (Ia) treatment group, thickening of the ear was significantly reduced to 30.8 ± 2.6% compared to the IMQ-control (FIG. 2A). Back skinfold thickness of the mice in the IMQ-control increased from 0.75 mm to 1.26 mm (FIG. 2B). Topical application of compound of formula (Ia) reduced skinfold thickness by 15.5 ± 4.0%, compared to the IMQ (FIG. 2B).

Example 2

Mannan-Induced Psoriasis in Mice

Study Design and Treatment

[0077] The 8- to 10-week-old male C57 mice (18-20 g) received a single dose of mannan from Saccharomyces cerevisiae (20 mg/kg, intraperitoneal route, dissolved in saline). To examine the efficacy of topical solution of desidustat, mice were randomly divided into 3 groups: Normal control, mannan control- model group (MAN control), and mannan (MAN) + 2.5% compound of formula (Ia) solution. Normal control animals were given normal saline instead of mannan. Treatment was started on day 0 along with injection of mannan and continued up to day 5. Right ear thickness was measured every day using thickness meter.

Results

[0078] Compound of formula (Ia) treatment reduces Mannan-induced ear thickness in mice

[0079] The right ear thickness was appeared to increase from day 2 to day 5 in MAN control group (FIG. 3). Treatment with 2.5% Compound of formula (Ia) reduced right ear thickness by 15.8 ± 2.5%, on day 5, when compared to MAN control group.

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