Method for the treatment of hyperproliferative disorders
AssigneeYale University
InventorsLeonard M. Milstone, Pauline M. Schwartz
Life of this patent
Estimating the term…
Abstract
The present invention provides new methods for the treatment of hyperproliferative disorders of skin epidermal cells, particularly psoriasis, by administering 5-fluorouracil and dipyridamole, with one or both agents being administered topically at the site of the hyperproliferative disease.
Claims8
A method for the treatment of hyperproliferative disorders of skin epidermal cells which comprises the concurrent administration to a patient of an efficacious amount of an inhibitor of the de novo pathway in DNA synthesis and an efficacious amount of an inhibitor of the salvage pathway in DNA synthesis, wherein the inhibitor of the de novo pathway is 5-fluorouracil and the inhibitor of the salvage pathway is dipyridamole, wherein the dipyridamole is administered topically at the site of the hyperproliferative disease and is applied at a concentration between about 0.1 and about 5 wt. %, and wherein the 5-fluorouracil is administered orally or by injection.
A method for the treatment of hyperproliferative disorders of skin epidermal cells which comprises the concurrent administration to a patient of an efficacious amount of an inhibitor of the de novo pathway in DNA synthesis and an efficacious amount of an inhibitor of the salvage pathway in DNA synthesis, wherein the inhibitor of the de novo pathway is 5-fluorouracil and the inhibitor of the salvage pathway is dipyridamole, wherein the 5-fluorouracil is administered topically at the site of the hyperproliferative disease and is applied at a concentration between about 0.1 and about 5 wt. %, and wherein the dipyridamole is administered orally or by injection.
A method for the treatment of hyperproliferative disorders of skin epidermal cells which comprises the concurrent administration to a patient of an efficacious amount of an inhibitor of the de novo pathway in DNA synthesis and an efficacious amount of an inhibitor of the salvage pathway in DNA synthesis, wherein the inhibitor of the de novo pathway is 5-fluorouracil and the inhibitor of the salvage pathway is dipyridamole, wherein the dipyridamole is administered topically at the site of the hyperproliferative disease and is applied at a concentration between about 0.1 and about 5 wt. %, and wherein the 5-fluorouracil is administered topically at the site of the hyperproliferative disease and is applied at a concentration between about 0.1 and about 5 wt. %.
Dependencies are inferred from the claim text.