Pharmaceutical composition comprising progestogens and/or estrogens and 5-methyl-(6S)-tetrahydrofolate
a technology of progestogens and/or estrogens, which is applied in the field of pharmaceutical compositions, can solve the problems of adversely affecting the utilizability of folic acid by the body and thus the biological activity of preventing neural tube defects, and achieve the effect of treating and preventing disorders caused by folate deficiency
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example 1
[0067]The composition of tablets (80 mg) of the invention can be found in Table 7.
TABLE 7Composition of tablets of the inventionAmountCompositionIngredientABCDDrospirenone3mg3mg—3mgEthinylestradiol*0.03mg0.02mg—0.03mgMetafolin0.451mg0.451mg0.451mg0.451mgVitamin B12———0.1mgLactose monohydrateto 80mgto 80mgto 80mgto 80mgCorn starch16.40mg16.40mg16.40mg16.40mgCorn starch**2mg***2mg***2mg***2mg***Modified corn9.60mg9.60mg9.60mg9.60mgstarchMagnesium stearate0.80mg0.80mg0.80mg0.80mg*optionally as ethinylestradiol-beta-cyclodextrin complex; the stated amount refers in this case to uncomplexed ethinylestradiol. If the ethinylestradiol-beta-cyclodextrin complex is used, about ten times the amount is to be employed. This is because the ethinylestradiol content in the β-cyclodextrin complex is about 9.5 to 12.5% (compare WO 02 / 49675).**the part of the corn starch identified by ** can be replaced by an alternative binder such as, for example, 1.6 mg of low-substituted hydroxypropyl-cellulose.**...
example 2
[0069]Blood is taken at 8-week intervals from 80 healthy young women of childbearing age, and the erythrocyte folate level is determined using a validated microbiological, immunological or instrumental (e.g. HPLC, LC-MS / MS) method or a suitable combination of these methods.
[0070]8 Weeks after the first blood sampling (screening phase), 451 μg of the calcium salt of 5-methyl-(6S)-tetrahydrofolic acid each day is administered over a period of 40 weeks or, alternatively: 3 mg of drospirenone, 30 μg of ethinylestradiol and 451 μg of the calcium salt of 5-methyl-(6S)-tetrahydrofolic acid is administered simultaneously on each of the first 21 days of the respective cycle (tablet of composition A in Example 1). Administration of 451 μg of the calcium salt of 5-methyl-(6S)-tetrahydrofolic acid is continued for 7 days in a phase immediately subsequent thereto (composition C). 3 mg of drospirenone, 30 μg of ethinylestradiol and 451 μg of the calcium salt of 5-methyl-(6S)-tetrahydrofolic acid ...
example 3
[0073]Blood is taken at 8-week intervals from 80 healthy young women of childbearing age, and the erythrocyte folate level is determined using a validated microbiological, immunological or instrumental (e.g. HPLC, LC-MS / MS) method or a suitable combination of these methods.
[0074]8 Weeks after the first blood sampling, 3 mg of drospirenone, 20 μg of ethinylestradiol and 451 μg of the calcium salt of 5-methyl-(6S)-tetrahydrofolic acid (composition B) is administered simultaneously in each case in the first 24 days of the respective cycle for a period of 40 weeks. In a phase immediately subsequent thereto, administration of 451 μg of the calcium salt of 5-methyl-(6S)-tetrahydrofolic acid is continued for 7 days (composition C). For a further 21 days (second cycle), 3 mg of drospirenone and 20 μg of ethinylestradiol and 451 μg of the calcium salt of 5-methyl-(6S)-tetrahydrofolic acid (composition B) are again administered, and only 451 μg of the calcium salt of 5-methyl-(6S)-tetrahydrof...
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