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.

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