The present invention relates to a nutritional supplement which comprises two different iron compounds, namely a rapidly dissolving iron compound and a slowly dissolving iron compound. The tablet is particularly contemplated for administration to women as a prenatal supplement, during pregnancy, and during lactation. Methods of alleviating iron deficiency and diseases and disorders associated therewith are also disclosed.
The present invention relates to a chewable, palatable oral contraceptive tablet, comprising an oral contraceptive agent, a chewable carrier suitable for human consumption, and not comprising a ferrocene compound, as well as use of these tablets in a method of human female oral contraception, and in a method of enhancing compliance with a human female oral contraceptive regimen.
Oral Pharmaceutical Products Containing 17 Β-Estradiol-3-Lower Alkanoate, Method Of Administering The Same And Process Of Preparation
Oluwole T. Aloba - Morristown NJ, US Tina M. deVries - Long Valley NJ, US
Assignee:
Warner Chilcott Company Inc. - Fajardo PR
International Classification:
A61K031/56 A01N025/08
US Classification:
514170, 514178, 424409
Abstract:
A pharmaceutical dosage unit for oral administration to a human female comprising a therapeutically effective amount of 17β-estradiol-3-lower alkanoate, most preferably 17β-estradiol-3-acetate, and a pharmaceutically acceptable carrier is disclosed. Also disclosed is a method for treating a human female in need of 17β-estradiol and a contraceptive method by oral administration of the pharmaceutical dosage unit and a method of preparing a pharmaceutical composition that may be used to form the pharmaceutical dosage unit of the invention.
Tina deVries - Long Valley NJ, US Lynn Gold - Seattle WA, US
Assignee:
Warner Chilcott Company, Inc. - Fajardo PR
International Classification:
A61K 9/14 A61K 9/20 A61K 9/28
US Classification:
424441, 424464, 424465, 424489
Abstract:
The present invention is a solid dosage form of a doxycycline metal complex. The present invention also includes a process for making a doxycycline metal complex in a solid dosage form. The process comprises the steps of (i) providing an aqueous solution of doxycycline or a physiologically acceptable salt thereof; (ii) admixing a metal salt with the aqueous solution; (iii) admixing a base to increase the pH of the aqueous solution, thereby forming a suspension of doxycycline metal; and (iv) drying the suspension, thereby forming a dry granulation of doxycycline metal complex.
Oral Pharmaceutical Products Containing 17Β-Estradiol-3-Lower Alkanoate, Method Of Administering The Same And Process Of Preparation
Oluwole T. Aloba - Morristown NJ, US Tina M deVries - Long Valley NJ, US
Assignee:
Warner Chilcott Company LLC - Fajardo PR
International Classification:
A61K 31/56 A01N 25/08
US Classification:
514170, 514178, 514171, 514182, 424409
Abstract:
A pharmaceutical dosage unit for oral administration to a human female comprising a therapeutically effective amount of 17β-estradiol-3-lower alkanoate, most preferably 17β-estradiol-3-acetate, and a pharmaceutically acceptable carrier is disclosed. Also disclosed is a method for treating a human female in need of 17β-estradiol and a contraceptive method by oral administration of the pharmaceutical dosage unit and a method of preparing a pharmaceutical composition that may be used to form the pharmaceutical dosage unit of the invention.
Oral Pharmaceutical Products Containing 17Β-Estradiol-3-Lower Alkanoate, Method Of Administering The Same And Process Of Preparation
Oluwole T. Aloba - Morristown NJ, US Tina M. deVries - Long Valley NJ, US
Assignee:
Warner Chilcott Company, LLC. - Fajardo PR
International Classification:
A61K 31/56 A01N 25/08
US Classification:
514182, 514170, 514178, 424409
Abstract:
A pharmaceutical dosage unit for oral administration to a human female comprising a therapeutically effective amount of 17β-estradiol-3-lower alkanoate, most preferably 17β-estradiol-3-acetate, and a pharmaceutically acceptable carrier is disclosed. Also disclosed is a method for treating a human female in need of 17β-estradiol and a contraceptive method by oral administration of the pharmaceutical dosage unit and a method of preparing a pharmaceutical composition that may be used to form the pharmaceutical dosage unit of the invention.
Tina deVries - Long Valley NJ, US Lynn Gold - Seattle WA, US
Assignee:
Warner Chilcott Company, LLC - Fajardo PR
International Classification:
A61K 31/65 A61K 9/48 A61K 9/20
US Classification:
514152, 424451, 424464
Abstract:
The present invention is a solid dosage form of a doxycycline metal complex. The present invention also includes a process for making a doxycycline metal complex in a solid dosage form. The process comprises the steps of (i) providing an aqueous solution of doxycycline or a physiologically acceptable salt thereof; (ii) admixing a metal salt with the aqueous solution; (iii) admixing a base to increase the pH of the aqueous solution, thereby forming a suspension of doxycycline metal; and (iv) drying the suspension, thereby forming a dry granulation of doxycycline metal complex.
Method Of Intermittent Administration Of A Pharmaceutical For The Treatment Of Conditions Associated With A Female's Menstrual Cycle
Roger Boissonneault - Long Valley NJ, US Tina deVries - Long Valley NJ, US Herman Ellman - Boonton Township NJ, US Kathryn MacFarlane - Morristown NJ, US Kelly Smith - Mountain Lakes NJ, US
International Classification:
A61K031/56
US Classification:
514170000
Abstract:
The present invention is a method of non-continuous administration of a pharmaceutical to a female for a condition associated with the female's menstrual cycle, comprising ascertaining a number of days in the female's menstrual cycle, and then administering a daily first dosage, starting on the first or the second day of the menstrual cycle and continuing the daily administration for a first dosage period. Next administering a daily second dosage, starting on the day after the last daily first dosage was administered and continuing the daily administration of the second dosage for a second dosage period. Wherein either the first dosage is a placebo and the second dosage is the pharmaceutical, or the first dosage is the pharmaceutical and the second dosage is a placebo. Both the first dosages and the second dosages being contained in a single package.
Vice President, Clinical Pharmacology at Warner Chilcott
Location:
Greater New York City Area
Industry:
Pharmaceuticals
Work:
Warner Chilcott since 1996
Vice President, Clinical Pharmacology
Warner Chilcott 1996 - 2005
Vice President, Pharmaceutics
Parke-Davis Research Division of Warner Lambert Sep 1989 - Apr 1996
Sr Research Associate
Education:
The Ohio State University 1983 - 1989
PhD, Pharmaceutics, Pharmaceutical Chemistry
Skills:
Oncology Regulatory Submissions Pharmaceutical Industry CRO Clinical Development Drug Discovery Clinical Trials IND Drug Development GMP Pharmaceutics
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