Non-hormonal compositions and methods for male contraception
The present invention relates to non-hormonal compositions and methods for inducing a condition of aspermia, azoospermia, or severe oligozoospermia in the male subject such that these compositions and methods for administering the same may be used as male contraception. Embodiments of the present invention may comprise a composition comprising an alpha-1-adrenoreceptor antagonist, such as (R)-silodosin, for daily administration to a male subject. The compositions and related methods may further include pharmaceutically acceptable carriers. The present invention further includes formulations which allow for a delay such that delayed or missed dose(s) do not nullify the contraceptive effect of the treatment regimen. Such compositions and methods may also avoid the side effects associated with typical formulations of alpha-1-adrenoreceptor antagonists.
1. A method for reversible, continuous non-hormonal contraception in a male subject, the method comprising administering once daily at about the same time, an oral dose of a composition comprising:
(i) an extended release formulation of (R)-silodosin in an amount effective, when administered once daily at about the same time, to induce a reversible condition of aspermia, azoospermia or severe oligozoospermia sufficient for contraceptive effect in the male subject; and
(ii) a pharmaceutically acceptable carrier,
wherein once daily administration of the formulation at about the same time provides a reversible contraceptive effect, but does not affect the quality of orgasm in the male subject.
2. The method of claim 1 , wherein the quality of orgasm is measured on the Numerical Rating Scale for subjective quality of orgasm.
3. The method of claim 1 , wherein the amount of (R)-silodosin in the composition administered once daily at about the same time is about 4 to about 12 mg.
4. The method of claim 1 , wherein the amount of (R)-silodosin in the composition administered once daily at about the same time is about 8 mg.
5. A method for reversible, continuous non-hormonal contraception in a male subject, the method comprising administering once daily at about the same time, an oral dose of a composition comprising:
(i) an extended release formulation of (R)-silodosin in an amount effective, when administered once daily at about the same time, to induce a reversible condition of aspermia, azoospermia or severe oligozoospermia sufficient for contraceptive effect in the male subject; and
(ii) a pharmaceutically acceptable carrier,
wherein once daily administration of the formulation at about the same time provides a reversible contraceptive effect, but does not cause discomfort upon ejaculation in the male subject.
6. The method of claim 5 , wherein the amount of (R)-silodosin in the composition administered once daily at about the same time is about 4 to about 12 mg.
7. The method of claim 5 , wherein the amount of (R)-silodosin in the composition administered once daily at about the same time is about 8 mg.
8. A method for reversible, continuous non-hormonal contraception in a male subject, the method comprising administering once daily at about the same time, an oral dose of a composition comprising:
(i) an extended release formulation of (R)-silodosin in an amount effective, when administered once daily at about the same time, to induce a reversible condition of aspermia, azoospermia or severe oligozoospermia sufficient for contraceptive effect in the male subject; and
(ii) a pharmaceutically acceptable carrier,
wherein a delay in administering one daily dose after an initial period of at least two consecutive days with doses administered at about the same time does not affect the contraceptive effect in the male subject, wherein the delay does not exceed 2, 4, 6, 8, 10 12, 16, 20 or 24 hours from the day-before intake time.
9. The method of claim 8 , wherein the initial period of consecutive days is at least 5 days.
10. The method of claim 8 , wherein the amount of (R)-silodosin in the composition administered once daily at about the same time is about 4 to about 12 mg.
11. The method of claim 8 , wherein the amount of (R)-silodosin in the composition administered once daily at about the same time is about 8 mg.
12. The method of claim 8 , wherein the delay in administering one daily dose does not exceed 4 hours.
13. The method of claim 8 , wherein the delay in administering one daily dose does not exceed 6 hours.
14. The method of claim 8 , wherein the delay in administering one daily dose does not exceed 8 hours.
15. The method of claim 8 , wherein the delay in administering one daily dose does not exceed 10 hours.
16. The method of claim 8 , wherein the delay in administering one daily dose does not exceed 12 hours.