REMITTIVE EFFECTS OF TAPINAROF IN THE TREATMENT OF PLAQUE PSORIASIS, ATOPIC DERMATITIS, OR RADIATION DERMATITIS
Embodiments described herein are directed to methods for treating moderate to severe plaque psoriasis, atopic dermatitis, or radiation dermatitis in a subject comprising administering about 1.0% tapinarof in a topical composition to the affected areas of the subject once a day for an initial period of time until the plaque psoriasis, atopic dermatitis, or radiation dermatitis is clear at which time the administration is stopped, and reassessing the subject from about 3 months to about 12 months after administration is stopped to determine if further treatment is required. Also described is the remittive effect observed after once daily administration of 1% tapinarof cream.
1 . A method for treating plaque psoriasis in a subject in need thereof, comprising
a. applying a thin layer of about 1.0% tapinarof topical cream composition to the affected areas of the subject once a day for an initial period of time of about 12 weeks to about 52 weeks, until the subject has a PGA score of 0;
b. after the initial period of time, stop treating the subject with tapinarof for a remittive period of time of about 1 to about 7 months, wherein the remittive period of time is the time wherein the subject maintains a PGA score <2; and
c. after the remittive period of time further applying a thin layer of 1.0% tapinarof topical cream composition to the affected areas of the subject once a day for a further period of time, until the subject has a PGA score of 0;
wherein
the 1.0% tapinarof topical cream composition does not prolong the QTc interval in the subject while applying the 1.0% tapinarof topical cream,
the plasma concentration of tapinarof in the subject is below 50 pg/mL while applying the 1.0% tapinarof topical cream, and
no tachyphylaxis occurs when further applying the thin layer of 1.0% tapinarof topical cream composition to the affected areas of the subject once a day for the initial period of time and the further period of time.
2 . (canceled)
3 . A method for treating plaque psoriasis in a subject in need thereof, wherein the subject has a PGA score of at least 1 point lower than baseline but has not achieved a PGA score of 0 after applying a thin layer of about 1.0% tapinarof topical cream composition to the affected areas of the subject once a day for a period of time of about 12 weeks to about 52 weeks comprising
applying a thin layer of about 1.0% tapinarof topical cream composition to the affected areas of the subject once a day for an indefinite period of time, wherein the PGA score does not increase when applying a thin layer of about 1.0% tapinarof topical cream composition to the affected areas of the subject once a day;
wherein
the 1.0% tapinarof topical cream composition does not prolong the QTc interval in the subject while applying the 1.0% tapinarof topical cream,
the plasma concentration of tapinarof in the subject is below 50 pg/mL while applying the 1.0% tapinarof topical cream, and
no tachyphylaxis occurs when applying the thin layer of 1.0% tapinarof topical cream composition to the affected areas of the subject once a day for the period of time of about 12 weeks to about 52 weeks and for the further period of time.
4 . The method of claim 3 , wherein the plaque psoriasis is moderate or severe plaque psoriasis.
5 . (canceled)
6 . (canceled)
7 . (canceled)
8 . (canceled)
9 . (canceled)
10 . (canceled)
11 . (canceled)
12 . The method of claim 1 , wherein the plaque psoriasis is moderate or severe plaque psoriasis.
13 . The method of claim 1 wherein the remittive period is greater than 3 months and up to about 7 months.
14 . The method of claim 1 wherein the remittive period is about 4 months.
15 . The method of claim 1 wherein the further period of time is less than the initial period of time.
16 . (canceled)
17 . (canceled)
18 . (canceled)
19 . (canceled)
20 . (canceled)
21 . The method of claim 1 , wherein the subject's itch numeric rating scale is improved by about 1 point to about 5 points at the end of the initial period of time.
22 . The method of claim 1 , wherein the subject's itch numeric rating scale is improved by about 4 points at the end of the initial period of time.
23 . The method of claim 1 , wherein the subject's Psoriasis Area and Severity Index (PASI) score is improved by at least 75% at the end of the initial period of time.
24 . The method of claim 1 , wherein the subject's Psoriasis Area and Severity Index (PASI) score is improved by at least 90% at the end of the initial period of time.
25 . The method of claim 1 , wherein the subject's percent body surface area (BSA) affected is decreased.
26 . The method of claim 3 , wherein the subject's itch numeric rating scale is improved by at least 1 point at the end of the initial period of time.
27 . The method of claim 3 , wherein the subject's Eczema Area and Severity Index (EASI) score is improved by at least 50% at the end of the initial period of time.
28 . The method of claim 1 , wherein the subject's percent body surface area (BSA) affected is decreased.