|
 |
| home > ebr > spring 2004 > the challenges in the development of hormonal preparations for women of a reproductive age |
 |
 |
PUBLICATIONS |
European BioPharmaceutical Review
|
| The majority of women use hormonal preparations in the course of their lives, mainly for contraception. In the past, new drugs were tested in men only, due to the potential risks of foetal harm should a woman become pregnant. Yet nowadays it has become widely acceptable to develop preparations in young, healthy women, according to a guideline from the Food and Drug Administration (FDA, 1993). So with no restriction on the participation of women with childbearing potential in all phases of drug trials, we now see gender analysis which pays special attention to factors affecting pharmacokinetics, such as the role of the menstrual cycle and exogenous hormone therapy in relation to the drug, as well as the influence of the drug on oral contraceptives. |
Read full article >>
|
 |
 |
 |
| Rate this article |
You must be a member of the site to make a vote. |
|
Average rating: |
0 |
| | | | | |
|
 |
By Doris Heger-Mahn, Medical Director and Executive, Astrid Breitschaft, Sub-Investigator and Marjo Ramakers, Research Physician at dinox Clinical Research
Doris Heger-Mahn has been a Medical Director and Executive at dinox since 1999. During the previous 10 years Doris held a number of positions at Schering AG, initially specialising in the assessment of female hormonal drugs, before moving into clinical development oncology and clinical operations. Her expertise lies in the development of drugs for female health. Doris completed her medical studies at the Free University Hospital in Berlin in 1986, and became a specialist in clinical pharmacology.
Astrid Breitschaft has been a Sub-Investigator at dinox since 2003. She began her career as a physician at the Robert-Rössle hospital, which is part of the University Hospital Charité in Berlin, participating in several oncology clinical trials. Astrid is currently working on her dissertation, which evaluates the influence of blood group constellations on the duration of transfusion dependency after ABO incompatible haematopoietic stem cell transplantation. She completed her medical studies at the Free University in Berlin in 1997.
Marjo Ramakers is a registered Sexologist, and has been conducting sexological clinical trials at dinox since 2002. In 1993 she founded a sexology outpatient clinic and for the next seven years worked at the Department of Sexology and Psychosomatic Gynaecology in the Academic Medical Center in Amsterdam, where she specialised in diagnosis and treatment of vulvodynia, dyspareunia and pelvic floor dysfunction. Marjo is currently writing a treatise on new outpatient clinic sexology.
|
|
 |
 |
 |
|

 |
Industry Events |
 |
Inaugural Conference on Pre-Filled Syringes
21-22 January 2009, Crowne Plaza Hotel - St James, London, UK
SMi present their Inaugural Conference on Pre-Filled Syringes 21st and 22nd January 2009 at the Crowne Plaza Hotel - St James, London, UK
More info >> |
|
 |
News and Press Releases |
 |
Azopharma Product Development Group, Inc
HOLLYWOOD, Fla. – Azopharma Product Development Group, Inc. (“Azopharma”) announced today the addition of innovative state-of-the-art equipment at its formulation and manufacturing division, ApiCross Drug Delivery Technologies in Hollywood, Florida. The most recent acquisition is the MG Futura Capsule Filler which delivers the latest in capsule filling technology. The company has also added a Bausch & Strobel Aseptic Filling Isolator, equipment that is ground-breaking in the powder filling process. These additions support our previously implemented XcelodoseTM powder micro-dosing system. With these technologies, Azopharma is able to provide its clients with all forms of the capsule filling process. The new equipment is part of Azopharma’s recent manufacturing expansion which includes 17 new manufacturing suites for GMP, cytotoxic and aseptic products...
More info >> |
|
|