Claims for Patent: 11,590,088

Summary for Patent: 11,590,088

Title:	Use of Tapinarof for the treatment of chronic plaque psoriasis
Abstract:	Topical compositions and methods for using topical compositions comprising tapinarof to treat mild to moderate atopic dermatitis or plaque psoriasis are described herein. Also described are clinical endpoints for treatment of subjects diagnosed with mild to moderate atopic dermatitis, wherein about 5% to about 35% of body surface area was affected, and Investigator Global Assessment (IGA) score was greater than or equal to 3. Also described are clinical endpoints for treatment of subjects diagnosed with chronic mild to moderate plaque psoriasis for greater than or equal to 6 months, wherein about 3% to about 20% of body surface area was affected, and Physician Global Assessment (PGA) score was greater than or equal to 2.
Inventor(s):	John E. KRAUS, James Lee
Assignee:	Dermavant Sciences GmbH
Application Number:	US17/871,663
Patent Litigation and PTAB cases:	See patent lawsuits and PTAB cases for patent 11,590,088
Patent Claims:	1. A method for treating mild to severe plaque psoriasis in a subject comprising topically administering a topical composition containing about 1.0% tapinarof to affected areas of the subject once a day, wherein after topically administering the topical composition a Physician Global Assessment (PGA) score is improved by 2 grades or has improved to a score of 0 or 1. 2. The method of claim 1, wherein the topical composition is an oil-in-water emulsion. 3. The method of claim 2, wherein the oil phase of the oil-in-water emulsion is comprised of medium chain triglycerides, propylene glycol, non-ionic emulsifying wax, diethylene glycol monoethyl ether, polyoxyl stearyl ether-2, polysorbate 80, polyoxyl stearyl ether-20, benzoic acid, and butylated hydroxytoluene. 4. The method of claim 2, wherein the water phase of the oil-in-water emulsion is comprised of sodium citrate, edetate disodium, citric acid monohydrate, and water. 5. The method of claim 1, wherein the subject has a Fitzpatrick skin type of I, II, III, IV, V, or VI and treatment with the topical composition is effective. 6. The method of claim 1, wherein the topically administering includes application to the affected area of the skin selected from the group consisting of body, arms, legs, back, chest, buttocks, neck, scalp, fingernails, toenails, and combination thereof. 7. The method of claim 1, wherein the subject has been diagnosed with mild to severe plaque psoriasis having a percent body surface area (BSA) affected of about 3% to about 20%. 8. The method of claim 1, wherein the subject has been diagnosed with mild to severe plaque psoriasis having a Physician Global Assessment (PGA) score of greater than or equal to 2. 9. The method of claim 1, further comprising after topically administering the topical composition an improvement of one or more symptom of mild to severe plaque psoriasis as measured according to an assessment selected from the group consisting of Physician Global Assessment (PGA) score, Psoriasis Area and Severity Index (PAST), target lesion grading, Itch/Pruritus numeric rating scale, percent body surface area (BSA) affected, Psoriasis Symptom Diary (PSD), Dermatology Quality of Life Index (DLQI), or 36 Item Short Form Survey (SF-36). 10. The method of claim 9, wherein the percent body surface area (BSA) affected is decreased to less than 20% after topically administering the topical composition. 11. The method of claim 9, wherein the Psoriasis Area and Severity Index (PAST) percent improvement is greater than or equal to 75% after topically administering the topical composition. 12. The method of claim 9, wherein the Itch/Pruritus numeric rating scale is improved by 3 points after topically administering the topical composition. 13. The method of claim 9, wherein the Psoriasis Symptom Diary (PSD) demonstrated that subject's impressions of symptom severity was improved after topically administering the topical composition, wherein the symptoms are selected from the group consisting of severity of flaky skin, bother of flaky skin, severity of dry skin, bother of dry skin, severity of bleeding, bother of bleeding, severity of itching, bother of itching, stinging, burning, pain from skin cracking, psoriasis-related pain, scaling, noticeability of color, need to hide skin, avoidance of activities, and overall embarrassment. 14. The method of claim 9, wherein the Dermatology Quality of Life Index (DLQI) demonstrated improvement on the impact of one or more daily activities after topically administering the topical composition. 15. The method of claim 9, wherein the 36 Item Short Form Survey (SF-36) demonstrated improvement in the physical component score and/or mental component score after topically administering the topical composition. 16. The method of claim 9, wherein the one or more symptom is improved after about 2 weeks, about 4 weeks, or about 8 weeks of administering the topical composition. 17. The method of claim 9, wherein the improvement in one or more symptoms continues for about 4 weeks after administration of the topical composition has ceased. 18. The method of claim 1, wherein the PGA score is improved after about 2 weeks, about 4 weeks, or about 8 weeks of administering the topical composition. 19. The method of claim 1, wherein the improvement in PGA score continues for about 4 weeks after administration of the topical composition has ceased. 20. The method of claim 1, wherein the topically administering the topical composition containing about 1.0% tapinarof results in systemic exposure of tapinarof that is below the limit of detection. 21. The method of claim 1, wherein the subject has been diagnosed with mild to moderate plaque psoriasis having a percent body surface area (BSA) affected of about 3% to about 20%. 22. The method of claim 1, wherein the subject has been diagnosed with mild to moderate plaque psoriasis having a Physician Global Assessment (PGA) score of greater than or equal to 2.