Methods of treating and/or preventing actinic keratosis
The application pertains to methods of treating and/or preventing actinic keratosis, comprising administering a therapeutically effective amount of KX-01, to a subject in need thereof.
1 . A method of treating actinic keratosis comprising topically administering to a subject in need thereof a therapeutically effective amount of a compound of the following structure:
to an affected area of the subject, wherein the therapeutically effective amount is 0.5 mg to 4 mg in a daily single dose unit and wherein the affected area is 0.1 cm 2 to 100 cm 2 .
2 . The method of claim 1 , wherein the therapeutically effective amount is 0.5 mg to 3 mg.
3 . The method of claim 1 , wherein the therapeutically effective amount is 1 mg to 2.5 mg.
4 . The method of claim 1 , wherein the therapeutically effective amount is 1.3 mg to 2.5 mg.
5 . The method of claim 1 , wherein the therapeutically effective amount is 2.5 mg.
6 . The method of claim 1 , wherein the therapeutically effective amount is 1 mg to 4 mg.
7 . The method of claim 1 , wherein the therapeutically effective amount is 3 mg to 4 mg.
8 . The method of claim 1 , wherein the therapeutically effective amount is 3 mg.
9 . The method of claim 1 , wherein the affected area is 1 cm 2 to 100 cm 2 .
10 . The method of claim 1 , wherein the affected area is 5 cm 2 to 100 cm 2 .
11 . The method of claim 1 , wherein the affected area is 10 cm 2 to 100 cm 2 .
12 . The method of claim 1 , wherein the affected area is 100 cm 2 .
13 . The method of claim 7 , wherein the affected area is 1 cm 2 to 100 cm 2 .
14 . The method of claim 7 , wherein the affected area is 5 cm 2 to 100 cm 2 .
15 . The method of claim 7 , wherein the affected area is 10 cm 2 to 100 cm 2 .
16 . The method of claim 7 , wherein the affected area is 25 cm 2 to 100 cm 2 .
17 . The method of claim 7 , wherein the affected area is 100 cm 2 .
18 . The method of claim 1 , wherein the affected area is 0.1 cm 2 to 25 cm 2 .
19 . The method of claim 1 , wherein the affected area is 1 cm 2 to 25 cm 2 .
20 . The method of claim 1 , wherein the affected area is 5 cm 2 to 25 cm 2 .
21 . The method of claim 1 , wherein the affected area is 10 cm 2 to 25 cm 2 .
22 . The method of claim 1 , wherein the affected area is 25 cm 2 .
23 . The method of claim 5 , wherein the affected area is 1 cm 2 to 25 cm 2 .
24 . The method of claim 5 , wherein the affected area is 5 cm 2 to 25 cm 2 .
25 . The method of claim 5 , wherein the affected area is 10 cm 2 to 25 cm 2 .
26 . The method of claim 5 , wherein the affected area is 25 cm 2 .
27 . The method of claim 1 , wherein the therapeutically effective amount is 0.035 mg/cm 2 .
28 . The method of claim 1 , wherein the therapeutically effective amount is 0.1 mg/cm 2 .
29 . The method of claim 1 , wherein the compound is administered once a day.
30 . The method of claim 5 , wherein the compound is administered once a day.
31 . The method of claim 7 , wherein the compound is administered once a day.
32 . The method of claim 17 , wherein the compound is administered once a day.
33 . The method of claim 26 , wherein the compound is administered once a day.
34 . The method of claim 27 , wherein the compound is administered once a day.
35 . The method of claim 28 , wherein the compound is administered once a day.
36 . The method of claim 1 , wherein the compound is administered once a day for 5 consecutive days.
37 . The method of claim 5 , wherein the compound is administered once a day for 5 consecutive days.
38 . The method of claim 7 , wherein the compound is administered once a day for 5 consecutive days.
39 . A method of treating actinic keratosis comprising topically administering to a subject in need thereof a therapeutically effective amount of a compound of the following structure:
to an affected area of the subject, wherein the therapeutically effective amount is 0.5 mg to 4 mg and wherein the affected area is 0.1 cm 2 to 100 cm 2 , wherein the affected area is the face or scalp.
40 . The method of claim 39 , wherein the therapeutically effective amount is 3 mg to 4 mg, the affected area is 100 cm 2 , and the compound is administered once a day for 5 consecutive days.
41 . The method of claim 39 , wherein the therapeutically effective amount is 2.5 mg, the affected area is 25 cm 2 , the compound is administered once a day for 5 consecutive days.
42 . The method of claim 39 , wherein the therapeutically effective amount is 0.035 mg/cm 2 and the compound is administered once a day for 5 consecutive days.
43 . The method of claim 39 , wherein the therapeutically effective amount is 0.1 mg/cm 2 and the compound is administered once a day for 5 consecutive days.
44 . The method of claim 1 , wherein the therapeutically effective amount is 3 mg to 4 mg, the affected area is 100 cm 2 , and the compound is provided in a daily single-dose unit administered once a day for 5 consecutive days.
45 . The method of claim 1 , wherein the therapeutically effective amount is 2.5 mg, the affected area is 25 cm 2 , and the compound is provided in a daily single-dose unit administered once a day for 5 consecutive days.
46 . The method of claim 1 , wherein the therapeutically effective amount is 0.035 mg/cm 2 , and the compound is provided in a daily single-dose unit administered once a day for 5 consecutive days.
47 . The method of claim 1 , wherein the therapeutically effective amount is 0.1 mg/cm 2 , and the compound is provided in a daily single-dose unit administered once a day for 5 consecutive days.
48 . The method of claim 1 , wherein the therapeutically effective amount is 0.035 mg/cm 2 , the affected area is the face or scalp and the compound is provided in a daily single-dose unit administered once a day for 5 consecutive days.
49 . The method of claim 1 , wherein the therapeutically effective amount is 0.1 mg/cm 2 , the affected area is the face or scalp and the compound is provided in a daily single-dose unit administered once a day for 5 consecutive days.
50 . The method of claim 1 , wherein the compound is topically administered to an affected area on the face or scalp of a subject in need thereof, once a day for 5 consecutive days at a single-dose unit of 2.5 mg to 4 mg over an affected area of 1 cm 2 to 100 cm 2 .
51 . The method of claim 50 , wherein the single-dose unit is 3 mg to 4 mg.
52 . The method of claim 51 , wherein the affected area is 1 cm 2 to 25 cm 2 .
53 . The method of claim 51 , wherein the affected area is 25 cm 2 to 100 cm 2 .
54 . The method of claim 50 , wherein the single-dose unit is 2.5 mg.
55 . The method of claim 54 , wherein the affected area is 1 cm 2 to 25 cm 2 .
56 . The method of claim 54 , wherein the affected area is 25 cm 2 to 100 cm 2 .
57 . The method of claim 54 , wherein the affected area is 100 cm 2 .