IP Library Granted Patent US 8,071,577
Granted Patent B2
US 8,071,577 · App. 11/578,771 · Granted Dec 6, 2011

Multi-phase contraceptive preparation based on a natural estrogen

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Quick Facts
Patent No.
US 8,071,577
App. No.
11/578,771
Granted
Dec 6, 2011
Kind
B2
Abstract

The multiphase preparation having higher contraceptive safety and reduced side effects is based on a combination of a natural oestrogen with dienogest or drospirenone. The multiphase preparation is characterized by a first phase consisting of 2 daily dose units of 3 mg of oestradiol valerate, a second phase consisting of 2 groups of daily dose units, wherein a first group is formed by 5 daily dose units each containing a combination of 2 mg of oestradiol valerate and at least two or three times an ovulation-inhibitory dose of dienogest or drospirenone and a second group is formed by 17 daily dose units each containing a combination of 2 mg of oestradiol valerate and at least three or four times the ovulation-inhibitory dose of dienogest or drospirenone, a third phase consisting of 2 daily dose units of 1 mg of oestradiol valerate, and a further phase consisting of 2 daily dose units of pharmaceutically acceptable placebo.

Claims (16)

1. A multiphase product for contraception comprising:

a first phase of 2 daily dosage units, each comprising 3 mg of estradiol valerate,

a second phase of 2 groups of daily dosage units, a first group comprising 5 daily dosage units, each of which comprises 2 mg of estradiol valerate and 2 mg of dienogest, and a second group comprising 17 daily dosage units, each of which comprises 2 mg of estradiol valerate and 3 mg of dienogest;

a third phase of 2 two daily dosage units, each comprising 1 mg of estradiol valerate, and

a fourth phase of 2 two daily dosage units, each comprising a pharmaceutically acceptable placebo.

2. A multiphase oral contraception product comprising:

a first phase of 2 daily oral dosage units, each comprising 3 mg of estradiol valerate,

a second phase of 2 groups of daily oral dosage units, a first group comprising 5 daily oral dosage units, each of which comprises 2 mg of estradiol valerate and 2 mg of dienogest, and a second group comprising 17 daily oral dosage units, each of which comprises 2 mg of estradiol valerate and 3 mg of dienogest;

a third phase of 2 daily oral dosage units, each comprising 1 mg of estradiol valerate, and

a fourth phase of 2 daily oral dosage units, each comprising a pharmaceutically acceptable placebo.

3. A method of oral contraception comprising orally administering to a woman:

one oral dosage unit comprising 3 mg of estradiol valerate daily for 2 days,

then one oral dosage unit comprising 2 mg of estradiol valerate and 2 mg of dienogest daily for 5 days,

then one oral dosage unit comprising 2 mg of estradiol valerate and 3 mg of dienogest daily for 17 days,

then one oral dosage unit comprising 1 mg of estradiol valerate daily for 2 days, and

then one oral dosage unit comprising a pharmaceutically acceptable placebo daily for 2 days.

Assignments (5)
CHANGE OF ADDRESS Recorded Jun 12, 2023
From: BAYER INTELLECTUAL PROPERTY GMBH
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 064021/0344 →
CHANGE OF NAME Recorded Apr 23, 2013
From: BAYER PHARMA AKTIENGESELLSCHAFT
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 030281/0953 →
CHANGE OF NAME Recorded Sep 28, 2011
From: BAYER SCHERING PHARMA AKTIENGESELLSCHAFT
To: BAYER PHARMA AKTIENGESELLSCHAFT
Reel/Frame 026983/0221 →
CHANGE OF NAME Recorded Nov 14, 2007
From: SCHERING AKTIENGESELLSCHAFT
To: BAYER SCHERING PHARMA AKTIENGESELLSCHAFT
Reel/Frame 020110/0334 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 28, 2007
From: ENDRIKAT, JAN; DUESTERBERG, BERND
To: BAYER SCHERING PHARMA AG
Reel/Frame 019755/0521 →