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A Novel Method for Involving Women of Color at High Risk for Preterm Birth in Research Priority Setting
Published on: January 12, 2018
Women and babies are dying from inertia: a collaborative framework for obstetrical drug development is urgently
Edith Roset Bahmanyar1, Henk J Out2, Marcel van Duin3
1Research and Development Department, Reproductive Medicine and Maternal Health, Ferring International Center SA, St Prex, Switzerland.
Insights
Developing new treatments for obstetrical complications is challenging due to safety concerns, poor understanding of pregnancy pathophysiology, and regulatory hurdles. Innovative therapies require significant investment and collaborative efforts to improve maternal and infant health.
Area of Science:
- Obstetrics and Gynecology
- Maternal-Fetal Medicine
- Pharmaceutical Research and Development
Background:
- Obstetrical complications, or great obstetrical syndromes, are leading causes of maternal and infant mortality and morbidity globally.
- Current treatments for these conditions are significantly underdeveloped compared to other medical fields, highlighting an urgent unmet need.
- Drug development in pregnancy faces unique challenges, including concerns for maternal, fetal, and infant safety, which reduce pharmaceutical investment.
Purpose of the Study:
- To identify and analyze the key pharmaceutical research and development challenges hindering the creation of effective and safe treatments for obstetrical syndromes.
- To explore the factors contributing to the paucity of innovative therapies for pregnancy complications.
- To propose solutions and foster stakeholder collaboration to advance drug development in obstetrics.
Main Methods:
- Literature review and analysis of existing research on pharmaceutical development in obstetrics.
- Examination of factors influencing investment decisions by pharmaceutical companies.
- Discussion of regulatory, ethical, and scientific barriers in clinical development for pregnancy complications.
Main Results:
- Pharmaceutical investment is limited by safety concerns, poorly defined syndromes, and complex regulatory pathways.
- A lack of understanding of obstetrical syndrome pathophysiology and limited preclinical de-risking strategies impede drug candidate discovery.
- Ethical review boards' reluctance to approve trials involving pregnant women and unpredictable regulatory guidance further complicate development.
Conclusions:
- Substantial commitment and investment are required to develop innovative therapies for pregnancy complications.
- An enabling ethical, legislative, and guidance framework is essential to facilitate progress in obstetrical drug development.
- Addressing this unmet need necessitates collaboration among all stakeholders, including patients, clinicians, and researchers.
Abstract:
Obstetrical complications, often referred to as the "great obstetrical syndromes," are among the most common global causes of mortality and morbidity in young women and their infants. However, treatments for these syndromes are underdeveloped compared with other fields of medicine and are urgently needed. This current paucity of treatments for obstetrical complications is a reflection of the challenges of drug development in pregnancy. The appetite of pharmaceutical companies to invest in research for obstetrical syndromes is generally reduced by concerns for maternal, fetal, and infant safety, poor definition, and high-risk regulatory paths toward product approval. Notably, drug candidates require large investments for development with an unguaranteed return on investment. Furthermore, the discovery of promising drug candidates is hampered by a poor understanding of the pathophysiology of obstetrical syndromes and their uniqueness to human pregnancies. This limits translational extrapolation and de-risking strategies in preclinical studies, as available for other medical areas, compounded with limited fetal safety monitoring to capture early prenatal adverse reactions. In addition, the ethical review committees are reluctant to approve the inclusion of pregnant women in trials, and in the absence of regulatory guidance in obstetrics, clinical development programs are subject to unpredictable regulatory paths. To develop effective and safe drugs for pregnancy complications, substantial commitment, and investment in research for innovative therapies are needed in parallel with the creation of an enabling ethical, legislative, and guidance framework. Solutions are proposed to enable stakeholders to work with a common set of expectations to facilitate progress in this medical discipline. Addressing this significant unmet need to advance maternal and possibly perinatal health requires the involvement of all stakeholders and specifically patients, couples, and clinicians facing pregnancy complications in the dearth of appropriate therapies. This paper focused on the key pharmaceutical research and development challenges to achieve effective and safe treatments for obstetrical syndromes.
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