Extended cycle multiphasic oral contraceptive kit
View Patent ↗A multiphasic contraceptive kit for use to practice a multiphasic method of contraception that provides for sequentially administering to a female of child bearing age: (a) a Phase I composition containing a progestogen and an estrogen for about 4 to about 7 days; (b) a Phase II composition containing a progestogen and an estrogen for about 8 to about 16 days; (c) a Phase III composition containing a progestogen and an estrogen for about 4 to about 7 days; and (d) optionally, a Phase IV composition which is a placebo or a non-steroidal component, wherein the ethinyl estradiol equivalent amount of estrogen in the Phase II composition is at least 5 mcg greater than the ethinyl estradiol equivalent amount of estrogen in each of the Phase I and III compositions. Preferably the sequential administration is repeated the day following the completion of the administration of the Phase III compositions providing an extended cycle multiphasic oral contraceptive method.
1. A multiphase combination and contraceptive kit comprising a package containing daily dosages of:
(a) a Phase I composition containing a progestogen in an amount equivalent to about 0.5 to about 1.5 mg of norethindrone acetate and an estrogen in an amount equivalent to about 5 to about 30 mcg of ethinyl estradiol;
(b) a Phase II composition containing a progestogen in an amount equivalent to about 0.5 to about 1.5 mg of norethindrone acetate and an estrogen in an amount equivalent to about 10 to about 40 mcg of ethinyl estradiol; and
(c) a Phase III composition a progestogen in an amount equivalent to containing about 0.5 to about 1.5 mg of norethindrone acetate and an estrogen in an amount equivalent to about 5 to about 30 mcg of ethinyl estradiol;
wherein the ethinyl estradiol equivalent amount of estrogen in the Phase II composition is at least 5 mcg greater than the ethinyl estradiol equivalent amount of estrogen in each of the Phase I and III compositions, wherein the ethinyl estradiol equivalent amount of estrogen in the Phase III composition is equal to the ethinyl estradiol equivalent amount of estrogen in the Phase I composition, and wherein the sequential administration of the Phase I, II, and III compositions is repeated the day following the completion of the administration of composition III to provide an extended contraceptive cycle, there is no decrease in the norethindrone acetate equivalent amount of progestogen from the administration of the Phase III composition to the administration of the Phase I composition in the extended contraceptive cycle and the extended contraceptive cycle is from about 42 to about 140 days.
2. The kit according to claim 1 , wherein the progestogen is selected from the group consisting of norethindrone acetate, drospirenone, trimegestone, norethindrone, levonorgestrel, desogestrel, 3-ketodesogestrel, gestodene, and mixtures thereof.
3. The kit according to claim 2 , wherein the progestogen is norethindrone acetate.
4. The kit according to claim 1 , wherein the estrogen is selected from the group consisting of ethinyl estradiol, 17β-estradiol, estradiol acetate, conjugated estrogens, mestranol, estrone, and salts thereof.
5. The kit according to claim 4 , wherein the estrogen is ethinyl estradiol.
6. The kit according to claim 1 , wherein the kit further comprises about 2 to about 9 dosages of a Phase IV composition which is a placebo or a non-steroidal component to be administered upon completion of the extended contraceptive cycle.
7. The kit according to claim 6 , wherein the norethindrone acetate equivalent amount of progestogen in the Phase I, II and III compositions is about 1 mg of norethindrone acetate.
8. The kit according to claim 7 , wherein the ethinyl estradiol equivalent amount of estrogen in the Phase I composition is about 25 mcg ethinyl estradiol, the ethinyl estradiol equivalent amount of estrogen in the Phase II composition is about 30 mcg of ethinyl estradiol, the ethinyl estradiol equivalent amount of estrogen in the Phase III composition is about 25 mcg of ethinyl estradiol, and the Phase IV composition contains about 75 mg of ferrous fumarate.
9. The kit according to claim 8 , wherein the estrogen and progestogen in the Phase I, II and III compositions are, respectively, ethinyl estradiol and norethindrone acetate.
10. The kit according to claim 7 , wherein the ethinyl estradiol equivalent amount of estrogen in the Phase I composition is about 20 mcg ethinyl estradiol, the ethinyl estradiol equivalent amount of estrogen in the Phase II composition is about 25 mcg of ethinyl estradiol, the ethinyl estradiol equivalent amount of estrogen in the Phase III composition is about 20 mcg of ethinyl estradiol, and the Phase IV composition contains about 75 mg of ferrous fumarate.
11. The kit according to claim 10 , wherein the estrogen and progestogen in the Phase I, II and III compositions are, respectively, ethinyl estradiol and norethindrone acetate.
12. The kit according to claim 1 , wherein the kit contains a plurality of groups of dosages of Phase I, II, and III compositions, wherein each group of dosages of Phase I composition contains about 4 to about 7 dosages, each group of dosages of Phase II compositions contains about 8 to about 16 dosages and each group of dosages of Phase III compositions contains about 4 to about 7 dosages.
13. The kit according to claim 12 , wherein the number of groups of dosages of Phase I, II, and III compositions is from about 2 to about 9.
14. The kit according to claim 13 , wherein said kit contains one group of dosages of a Phase IV composition that amounts to about 2 to about 9 daily dosages.
15. The kit according to claim 14 , wherein the norethindrone acetate equivalent amount of progestogen in the Phase I, II, and III compositions is about 1 mg of norethindrone acetate.
16. The kit according to claim 15 , wherein the ethinyl estradiol equivalent amount of estrogen in the Phase I composition is about 20 mcg of ethinyl estradiol, the ethinyl estradiol equivalent amount of estrogen in the Phase II composition is about 25 mcg of ethinyl estradiol, and the ethinyl estradiol equivalent amount of estrogen in the Phase III composition is about 20 mcg of ethinyl estradiol.
17. The kit according to claim 16 , wherein the estrogen and progestogen in the Phase I, II and III compositions are, respectively, ethinyl estradiol and norethindrone acetate.
18. The kit according to claim 17 , wherein each group of dosages of the Phase I composition contains about 5 dosages, each group of dosages of the Phase II composition contains about 11 to about 14 dosages, and each group of dosages of the Phase III composition contains about 5 dosages.
19. The kit according to claim 15 , wherein the ethinyl estradiol equivalent amount of estrogen in the Phase I composition is about 25 mcg of ethinyl estradiol, the ethinyl estradiol equivalent amount of estrogen in the Phase II composition is about 30 mcg of ethinyl estradiol, and the ethinyl estradiol equivalent amount of estrogen in the Phase III composition is about 25 mcg of ethinyl estradiol.
20. The kit according to claim 19 , wherein the estrogen and progestogen in the Phase I, II and III compositions are, respectively, ethinyl estradiol and norethindrone acetate.
21. The kit according to claim 20 , wherein each group of dosages of the Phase I composition contains about 5 dosages, each group of dosages of the Phase II composition contains about 11 to about 14 dosages, and each group of dosages of the Phase III composition contains about 5 dosages.