http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6479475-B1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P15-18
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filingDate 1997-07-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2002-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 2002-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-6479475-B1
titleOfInvention Oral contraceptive
abstract This invention provides a method of contraception which comprises administering to a female of child bearing age for 23-25 consecutive days,a first phase combination of a progestin at a daily dosage of 40-500 mug trimegestone, 250 mug-4 mg dienogest, or 250 mug-4 mg drospirenone, and an estrogen at a daily dosage equivalent in estrogenic activity to 10-20 mug ethinyl estradiol for 3-8 days beginning on day 1 of the menstrual cycle, wherein the same dosage of the progestin and estrogen combination is administered in each of the 3-8 days,a second phase combination of a progeslin at a daily dosage of 40-500 mug trimegestone, 250 mug-4 mg dienogest, or 250 mug-4 mg drospirenone, and an estrogen at a daily dosage equivalent in estrogenic activity to 10-20 mug ethinyl estradiol, for 4-15 days beginning on the day immediately following the last day of administration of the first phase combination, wherein the same dosage of the progestin and estrogen combination is administered in each of the 4-15 days, anda third phase combination of a progestin at a daily dosage of 40-500 mug trimegestone, 250 mug-4 mg dienogest, or 250 mug-4 mg drospirenone, and an estrogen at a daily dosage equivalent in estrogenic activity to 10-20 mug ethinyl estradiol, for 4-15 days beginning on the day immediately following the last day of administration of the second phase combination, wherein the same dosage of the progestin and estrogen combination is administered in each of the 4-15 daysprovided that the daily dosage of the combination administered in the first phase is not the same as the daily dosage of the combination administered in the second phase and that the daily dosage of the combination administered in the second phase is not the same as the daily dosage of the combination administered in the third phase
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