Barriers and Opportunities in Therapeutic Development for Early-Onset Preeclampsia

Early-onset preeclampsia (EOPE) remains a major contributor to maternal and fetal/neonatal morbidity and mortality worldwide, with delivery, frequently at early preterm gestations, remaining the only effective way to halt disease progression. Therapeutic development has been limited by disease heterogeneity, unpredictable conditions, a progressive course, ethical and safety concerns in pregnancy, and uncertainty over trial design and regulatory pathways. This document summarizes an international multidisciplinary convening of clinicians, trialists, pharmacologists, regulators, and global health experts who met to explore key challenges and emerging strategies for therapeutic development in EOPE. Discussion centered on EOPE, marked by abnormal placentation, pronounced angiogenic imbalance, and high maternal-fetal risk, viewed as a potentially tractable target for disease-modifying interventions. Key themes included trial eligibility and enrollment, use of angiogenic biomarkers for enrichment and monitoring, defining meaningful maternal and fetal end points, safety oversight in the dual-patient context, and the potential of adaptive trial designs. Participants also considered translational tools such as pharmacokinetic (physiologically based pharmacokinetic) modeling and placental transfer studies. Participants identified both areas of alignment and continued uncertainty. Biologically informed strategies, such as biomarker-supported enrollment and carefully designed early-phase studies were seen as helpful in reducing uncertainty, especially alongside early regulatory engagement. Although many developers are pursuing soluble fms-like tyrosine kinase-1 as a therapeutic target for EOPE, participants stressed the need for further biomarker validation, careful maternal-fetal risk-benefit assessment, and globally feasible approaches. Though focused on EOPE, these discussions may inform future research on late-onset disease, given its distinct underlying biology.

Authors

Institutions

Publication Details

Journal
Hypertension
Published
2026-10-27
DOI
https://doi.org/10.1161/hypertensionaha.126.27415
Primary Topic
Pregnancy and preeclampsia studies
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Barriers and Opportunities in Therapeutic Development for Early-Onset Preeclampsia

Jon Anthony Hyett, Swati Bhat, S. Ananth Karumanchi, Joey P. Granger et al.
2 links
Hypertension
Pregnancy and preeclampsia studies
article

Barriers and Opportunities in Therapeutic Development for Early-Onset Preeclampsia

Jon Anthony Hyett, Swati Bhat, S. Ananth Karumanchi, Joey P. Granger, Corinne S de Vries, Kwame Adu‐Bonsaffoh, Manu Vatish, Holger Stepan, Priya Soma‐Pillay, Stephen Rulisa, Christina Chang, Sarosh Rana, Robyn Langham AM, Sailesh Kumar, An Massaro
article en

Abstract

Early-onset preeclampsia (EOPE) remains a major contributor to maternal and fetal/neonatal morbidity and mortality worldwide, with delivery, frequently at early preterm gestations, remaining the only effective way to halt disease progression. Therapeutic development has been limited by disease heterogeneity, unpredictable conditions, a progressive course, ethical and safety concerns in pregnancy, and uncertainty over trial design and regulatory pathways. This document summarizes an international multidisciplinary convening of clinicians, trialists, pharmacologists, regulators, and global health experts who met to explore key challenges and emerging strategies for therapeutic development in EOPE. Discussion centered on EOPE, marked by abnormal placentation, pronounced angiogenic imbalance, and high maternal-fetal risk, viewed as a potentially tractable target for disease-modifying interventions. Key themes included trial eligibility and enrollment, use of angiogenic biomarkers for enrichment and monitoring, defining meaningful maternal and fetal end points, safety oversight in the dual-patient context, and the potential of adaptive trial designs. Participants also considered translational tools such as pharmacokinetic (physiologically based pharmacokinetic) modeling and placental transfer studies. Participants identified both areas of alignment and continued uncertainty. Biologically informed strategies, such as biomarker-supported enrollment and carefully designed early-phase studies were seen as helpful in reducing uncertainty, especially alongside early regulatory engagement. Although many developers are pursuing soluble fms-like tyrosine kinase-1 as a therapeutic target for EOPE, participants stressed the need for further biomarker validation, careful maternal-fetal risk-benefit assessment, and globally feasible approaches. Though focused on EOPE, these discussions may inform future research on late-onset disease, given its distinct underlying biology.

Hypertension
Cedars-Sinai Medical Center (US), European Medicines Agency (NL), Gates Foundation (US), United States Food and Drug Administration (US), Center for Drug Evaluation and Research (US), University of Ghana (GH), The University of Queensland (AU), University of South Africa (ZA), Liverpool Hospital (AU), University of Nebraska System (US), University of Mississippi Medical Center (US), University of Rwanda (RW), Mater Research (AU), University Hospital Leipzig (DE), Ingham Institute (AU), Food and Drug Administration (TH), Medicines and Healthcare products Regulatory Agency (GB), University of Pretoria (ZA)
Bill and Melinda Gates Foundation, Cedars-Sinai Medical Center, University of Rwanda, University of Pretoria, University of Ghana, Ingham Institute for Applied Medical Research, U.S. Food and Drug Administration
Good health and well-being
Openalex Percentile: Top 8%
Pregnancy and preeclampsia studies
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Laika access coming soon