US2010197722A1PendingUtilityA1
Treatment for basal cell carcinoma
Assignee: GRACEWAY PHARMACEUTICALS LLCPriority: Mar 25, 2003Filed: Apr 2, 2010Published: Aug 5, 2010
Est. expiryMar 25, 2023(expired)· nominal 20-yr term from priority
A61K 9/0014A61K 47/12A61P 35/00A61K 31/44
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Claims
Abstract
The present invention provides a method of treating basal cell carcinoma in a subject. Generally, the method includes administering to the subject an amount of IRM compound effective for treating basal cell carcinoma in a treatment cycle that includes at least two consecutive days in which the IRM compound is administered and at least one day in which the IRM compound is not administered.
Claims
exact text as granted — not AI-modified1 . A method of treating basal cell carcinoma in a subject, the method comprising administering to the subject an amount of an IRM compound effective for treating basal cell carcinoma, wherein the IRM compound is administered in a treatment cycle that comprises at least two consecutive days in which the IRM compound is administered and at least one day in which the IRM compound is not administered.
2 . The method of claim 1 wherein the treatment cycle comprises at least five days in which the IRM compound is administered.
3 . The method of claim 2 wherein the treatment comprises at least five consecutive days in which the IRM compound is administered.
4 . The method of claim 1 wherein the treatment cycle comprises at least two consecutive days in which the IRM compound is not administered.
5 . The method of claim 1 wherein the treatment cycle comprises five days in which the IRM compound is administered and at least two days in which the IRM compound is not administered.
6 . The method of claim 5 wherein the five days are five consecutive days.
7 . The method of claim 1 wherein the method comprises at least two treatment cycles.
8 . The method of claim 7 wherein the method comprises at least six treatment cycles.
9 . The method of claim 1 wherein administering the IRM compound comprises applying one dose of the IRM compound per day.
10 . The method of claim 1 wherein administering the IRM compound comprises topically applying the IRM compound to a treatment area that includes a lesion.
11 . The method of claim 10 wherein the IRM compound is applied in a formulation that comprises from about 1% to about 10% IRM compound.
12 . The method of claim 11 wherein the formulation comprises about 5% IRM compound.
13 . The method of claim 11 wherein the formulation is applied to the treatment area for from about two hours to about 24 hours.
14 . The method of claim 13 wherein the formulation is applied to the treatment area for from about six hours to about twelve hours.
15 . The method of claim 11 wherein the formulation is applied to the treatment area for about eight hours.
16 . The method of claim 10 wherein the treatment area further comprises skin at least 0.5 cm beyond the margin of the lesion.Cited by (0)
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