Multiple agent therapy for sexual dysfunction
View Patent ↗Multiple agent therapy for treatment of sexual dysfunction, including male erectile dysfunction, with sequential administration a type V phosphodiesterase inhibitor (PDE-5), such as sildenafil, preferably wherein the PDE-5 inhibitor is administered by oral dose means, and a melanocortin 3 and/or 4 receptor agonist, such as Ac-Nle-cyclo(-Asp-His-D-Phe-Arg-Trp-Lys)-OH (PT-141) preferably wherein the PT-141 is formulated for and administered by intranasal means, and further preferably wherein the PDE-5 inhibitor is administered prior to PT-141.
1. A method of treating sexual dysfunction in a patient, comprising:
oral administration of a quantity of a type V phosphodiesterase (PDE-5) inhibitor; and
non-oral administration of a quantity of Ac-Nle-cyclo(-Asp-His-D-Phe-Arg-Trp-Lys)-OH (PT-141),
wherein the quantity of the PDE-5 inhibitor and the quantity of PT-141 are together sufficient to produce synergistic effect in the treatment of sexual dysfunction in the patient.
2. The method of claim 1 , wherein the non-oral administration of PT-141 is intranasal.
3. The method of claim 1 , wherein the quantity of PDE-5 inhibitor administered is not sufficient to initiate a desired pharmacological response in treating sexual dysfunction in the patient when administered as a monotherapy.
4. The method of claim 2 , wherein the quantity of PT-141 administered is not sufficient to initiate a desired pharmacological response in treating sexual dysfunction in the patient when administered as a monotherapy.
5. The method of claim 1 , wherein the patient is a male patient, the sexual dysfunction is erectile dysfunction, and a desired pharmacological response comprising the ability to attain an erection of sufficient rigidity for sexual intercourse, the ability to sustain an erection of sufficient rigidity for sexual intercourse or a combination thereof is obtained.
6. The method of claim 1 wherein the PDE-5 inhibitor is sildenafil, vardenafil or tadalafil.
7. The method of claim 6 , wherein the PDE-5 inhibitor is sildenafil, the quantity of sildenafil administered is between about 25 mg and about 100 mg and the quantity of PT-141 administered is between about 2.5 mg and about 15 mg.
8. The method of claim 6 , wherein the PDE-5 inhibitor is sildenafil, the quantity of sildenafil is about 25 mg and the quantity of PT-141 is about 7.5 mg.
9. The method of claim 6 , wherein the PDE-5 inhibitor is sildenafil, the quantity of sildenafil administered is no more than about 25 mg and the quantity of PT-141 administered is no more than about 10 mg.
10. The method of claim 1 , wherein the PDE-5 inhibitor is administered prior to administration of PT-141.
11. The method of claim 1 , wherein the PDE-5 inhibitor is administered between about 5 and 45 minutes prior to administration of PT-141.
12. The method of claim 1 , wherein the PDE-5 inhibitor is administered between about 10 and 30 minutes prior to administration of PT-141.
13. The method of claim 1 , wherein PT-141 is administered about 30 minutes prior to the attainment of the average peak plasma concentration (T max ) of the PDE-5 inhibitor.
14. The method of claim 1 , wherein PT-141 is administered no later than about 30 minutes prior to the end of the average half-life of the PDE-5 inhibitor.
15. The method of claim 1 , wherein the PDE-5 inhibitor is administered so as to maintain a steady-state plasma concentration and PT-141 is administered thereafter while the PDE-5 inhibitor is at the steady-state plasma concentration.
16. The method of claim 15 , wherein the PDE-5 inhibitor is tadalafil.
17. The method of claim 1 , wherein:
the patient is a male patient,
the sexual dysfunction is erectile dysfunction,
the quantity of PDE-5 inhibitor administered is less than that required to treat erectile dysfunction using the PDE-5 inhibitor as a monotherapy,
the quantity of PT-141 administered is less than that required to treat erectile dysfunction using PT-141 as a monotherapy, and
the quality of erection score obtained is superior to that obtained from (i) administration of the PDE-5 inhibitor as a monotherapy in a therapeutically effective amount sufficient to treat erectile dysfunction in the patient, or (ii) administration of PT-141 as a monotherapy in a therapeutically effective amount sufficient to treat erectile dysfunction in the patient.
18. A method of treating erectile dysfunction in a patient, comprising:
oral administration of a PDE-5 inhibitor; and
intranasal administration of a quantity of PT-141 of less than about 12 mg,
wherein the PDE-5 inhibitor is administered prior to intranasal administration of PT-141,
and wherein the quantity of the PDE-5 inhibitor and the quantity of PT-141 are together effective to treat erectile dysfunction in the patient.
19. A method of decreasing side effects associated with therapeutic agents for treating sexual dysfunction in a patient, comprising:
oral administration of a quantity of PDE-5 inhibitor, wherein the quantity of PDE-5 inhibitor administered is not sufficient to initiate a desired pharmacological response treating sexual dysfunction in the patient when administered as a monotherapy; and
non-oral administration of a quantity of PT-141, wherein the quantity of PT-141 administered is not sufficient to initiate the desired pharmacological response in treating sexual dysfunction in the patient when administered as a monotherapy,
wherein the quantity of the PDE-5 inhibitor and the quantity of PT-141 are together effective to initiate the desired pharmacological response in treating sexual dysfunction in the patient,
thereby reducing side effects in the treatment of sexual dysfunction in the patient.
20. A method of treating sexual dysfunction in a patient marginally responsive to a PDE-5 inhibitor, comprising the steps of:
establishing a dose of a PDE-5 inhibitor at which the patient has marginal responsiveness with respect to treating sexual dysfunction with the PDE-5 inhibitor;
oral administration of the marginally responsive dose of the PDE-5 inhibitor; and
non-oral administration of a Quantity of PT-141, wherein the dose of the PDE-5 inhibitor
and the Quantity of PT-141 are effective to increase the responsiveness with
respect to treating sexual dysfunction in the patient.
21. The method of claim 20 , wherein the step of establishing a dose of a PDE-5 inhibitor to which the patient is marginally responsive comprises:
establishing a dose of a PDE-5 inhibitor at which the patient is responsive about 25% to about 50% of the time.
22. The method of claim 20 , wherein sexual dysfunction is erectile dysfunction.