Estrogen replacement therapy
AssigneeWyeth
InventorJames H. Pickar
Life of this patent
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Abstract
This invention relates to methods and pharmaceutical compositions for providing estrogen replacement therapy in perimenopausal, menopausal, and postmenopausal women through the continuous administration of conjugated estrogens.
Claims51
A method of treating or inhibiting menopausal or postmenopausal disorders in a perimenopausal, menopausal, or postmenopausal woman in need thereof, which comprises orally providing to said woman continuously and uninterruptedly over the treatment period, a daily dosage of between about 0.25 mg and about 0.1 mg conjugated estrogens.
A method of treating or inhibiting vasomotor symptoms in a perimenopausal, menopausal, or postmenopausal woman in need thereof, which comprises orally providing to said woman continuously and uninterruptedly over the treatment period, a daily dosage of between about 0.25 mg and about 0.1 mg conjugated estrogens.
A method of inhibiting or retarding bone demineralization or treating or inhibiting osteoporosis in a perimenopausal, menopausal, or postmenopausal woman in need thereof, which comprises orally providing to said woman continuously and uninterruptedly over the treatment period, a daily dosage of between about 0.25 mg and about 0.1 mg conjugated estrogens.
A method of treating or inhibiting vaginal or vulvar atrophy;
- atrophic vaginitis;
- vaginal dryness;
- pruritus;
- dyspareunia;
- dysuria;
- frequent urination;
- urinary incontinence;
- urinary tract infections in a perimenopausal, menopausal, or postmenopausal woman in need thereof, which comprises orally providing to said woman continuously and uninterruptedly over the treatment period, a daily dosage of between about 0.25 mg and about 0.1 mg conjugated estrogens.
A method of lowering cholesterol, Lp(a), or LDL levels;
- inhibiting or treating hypercholesteremia;
- hyperlipidemia;
- cardiovascular disease;
- atherosclerosis;
- peripheral vascular disease;
- restenosis, vasospasm;
- or inhibiting vascular wall damage from cellular events leading toward immune mediated vascular damage, in a perimenopausal, menopausal, or postmenopausal woman in need thereof, which comprises orally providing to said woman continuously and uninterruptedly over the treatment period, a daily dosage of between about 0.25 mg and about 0.1 mg conjugated estrogens.
A method of treating or inhibiting free radical involvement in the development of cancers, central nervous system disorders, Alzheimer's disease, bone disease, aging, inflammatory disorders, peripheral vascular disease, rheumatoid arthritis, autoimmune diseases, respiratory distress, emphysema, prevention of reperfusion injury, viral hepatitis, chronic active hepatitis, tuberculosis, psoriasis, systemic lupus erythematosus, amyotrophic lateral sclerosis, aging effects, adult respiratory distress syndrome, central nervous system trauma and stroke, or injury during reperfusion procedures in a perimenopausal, menopausal, or postmenopausal woman in need thereof, which comprises orally providing to said woman continuously and uninterruptedly over the treatment period, a daily dosage of between about 0.25 mg and about 0.1 mg conjugated estrogens.
A method of treating or inhibiting dementias, neurodegenerative disorders, and Alzheimer's disease;
- providing neuroprotection or cognition enhancement in a perimenopausal, menopausal, or postmenopausal woman in need thereof, which comprises orally providing to said woman continuously and uninterruptedly over the treatment period, a daily dosage of between about 0.25 mg and about 0.1 mg conjugated estrogens.
The method according to claim 31, wherein the daily dosage of conjugated equine estrogens is between about 0.2 mg and about 0.1 mg.
A pharmaceutical composition for use in treating menopausal or postmenopausal disorders, which comprises dosage of between about 0.25 mg and about 0.1 mg conjugated estrogens, and a pharmaceutical carrier.
A pharmaceutical dosage unit which comprises which comprises conjugated estrogens, a dosage of between about 0.25 mg and about 0.1 mg conjugated estrogens and a pharmaceutical carrier.
A method of minimizing or reducing levels;
- of breast pain in a woman receiving hormone replacement therapy, which comprises orally providing to said woman continuously and uninterruptedly over the treatment period, a daily dosage of between about 0.25 mg and about 0.1 mg conjugated estrogens.
A method of minimizing spotting or breakthrough bleeding;
- or achieving amenorrhea in a woman receiving hormone replacement therapy, which comprises orally providing to said woman continuously and uninterruptedly over the treatment period, a daily dosage of between about 0.25 mg and about 0.1 mg.
A method of increasing bone mineral density in a perimenopausal, menopausal, or postmenopausal woman in need thereof, which comprises orally providing to said woman continuously and uninterruptedly over the treatment period, a daily dosage of between about 0.25 mg and about 0.1 mg conjugated estrogens.
Dependencies are inferred from the claim text.