Claims for Patent: 6,794,489

Summary for Patent: 6,794,489

Title:	Compositions and methods for treatment of sexual dysfunction
Abstract:	Compositions and methods are provided for treatment of sexual dysfunction in mammals, including male sexual dysfunction, such as erectile dysfunction, and female sexual dysfunction. In one embodiment, a peptide-based composition including the peptide sequence Ac-Nle-cyclo(-Asp-His-D-Phe-Arg-Trp-Lys)-OH is administered. Methods of administration include injection, oral, nasal and mucosal administration.
Inventor(s):	Blood; Christine H. (Morristown, NJ), Shadiack; Annette M. (Sommerset, NJ), Bernstein; Joanna K. (North Brunswick, NJ), Herbert; Guy H. (Metuchen, NJ)
Assignee:	Palatin Technologies, Inc. (Cranbury, NJ)
Application Number:	10/040,547
Patent Claims:	1. A pharmaceutical composition, comprising a peptide in a pharmaceutically acceptable aqueous carrier, wherein said peptide is a free acid or a pharmaceutically acceptable salt thereof comprising the sequence Nle-cyclo(-Arg-His-D-Phe-Arg-Trp-Lys)-OH. 2. The pharamceuticai composition of claim 1, wherein said peptide is cyclicized through the side chains of Asp and Lys without introduction of an additional molecular unit. 3. The pharmaceutical composition of claim 1, wherein said peptide has an acetylated amino group at amino terminus. 4. The pharmaceutical composition of claim 1, wherein the peptide consists of the sequence Ac-Nle-cyclo(-Asp-His-D-Phe-Arg-Trp-Lys)-OH. 5. A method for stimulating sexual response in a mammal, comprising administering a pharmaceutically sufficient amount of a composition comprising a peptide or pharmaceutically acceptable salt thereof of the formula Ac-Nle-cyclo(-Asp-His-D-Phe-Arg-Trp-Lys)-OH for a time and under conditions effective to stimulate a sexual response. 6. The method of claim 5, wherein the mammal is a male. 7. The method of claim 5, wherein the mammal is a female. 8. The method of claim 5, wherein the pharmaceutically sufficient amount is at a dose level that does not induce emesis or other deleterious side effects. 9. The method of claim of claim 5, wherein the composition further comprises a pharmaceutically acceptable carrier. 10. The method of claim 5, wherein administering comprises a method of administration selected from the group consisting of administration by injection, administration through mucous membranes, buccal administration, oral administration, dermal administration, inhalation administration and nasal administration. 11. The method of claim 10, wherein administering comprises nasal administration of a metered amount of a formulation comprising an aqueous buffer. 12. The method of claim 11, wherein the aqueous buffer is a member selected from the group consisting of saline and citrate buffer. 13. A purified peptide or pharmaceutically acceptable salt thereof consisting of Ac-Nle-cyclo(Asp-His-D-Phe-Arg-Trp-Lys)-OH. 14. An isolated peptide or pharmaceutically acceptable salt thereof consisting of Ac-Nle-cyclo(-Asp-His-D-Phe-Arg-Trp-Lys)-OH. 15. A pharmaceutical kit, comprising the pharmaceutical composition of claim 1 disposed in a nasal administration device. 16. The pharmaceutical kit of claim 15 wherein the nasal administration device is a metered dose nasal administration device. 17. The pharmaceutical kit of claim 16 wherein the metered dose nasal administration device dispenses a metered spray volume of approximately 100 .mu.L. 18. The pharmaceutical kit of claim 15 wherein the pharmaceutically acceptable salt is an acetate salt.