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Study identifier: NCT07738562 Synced from ClinicalTrials.gov · August 06, 2026
● Study status: Not Yet Recruiting

Dipyridamole for Early-Onset Preeclampsia: A Pilot Study of Feasibility, Pharmacokinetics, and Biological Effects

Condition: Preeclampsia (PE) · Hypertension ,Pregnancy  ·  Sponsor: Hadassah Medical Organization

PhasePhase 1/Phase 2
Planned participants15
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

Early-onset preeclampsia (PE), defined as preeclampsia presenting before 34 weeks of gestation, is a severe placental disorder associated with significant maternal and perinatal morbidity. There is currently no disease-modifying treatment; management relies on close surveillance and delivery, frequently resulting in extreme prematurity. Recent laboratory research identified ferroptosis, a form of iron-dependent regulated cell death driven by lipid peroxidation, as a key mechanism of placental injury in early-onset preeclampsia. A high-throughput drug screen identified dipyridamole, an approved oral antiplatelet and vasodilatory agent, as a potent ferroptosis inhibitor in primary human trophoblast cultures (EC50 = 0.146 µM), acting through mechanisms independent of its known phosphodiesterase-inhibitory pharmacology. In preeclamptic placental explants, dipyridamole markedly reduced release of sFlt-1, a central mediator of the maternal syndrome. Dipyridamole carries an established pregnancy safety record supported by randomized trials and a Cochrane meta-analysis of antiplatelet agents in pregnancy. This is a prospective, single-center, open-label pilot study using a sequential, fixed dose-escalation design. The study will enroll 15 hospitalized pregnant women with early-onset preeclampsia (gestational age 26+0 to 33+6 weeks) and an elevated sFlt-1/PlGF ratio (≥85), for whom expectant management is clinically appropriate. Enrollment proceeds through a staged sentinel design w…

This description comes directly from the study's public registry record.

Talk to the study team

Prof. Ofer Beharier, Principal Investigator  ·  972+586306700  ·  bofer@hadassah.org.il

Always discuss trial participation with your own doctor first.

Locations (1)

Hadassah University Medical CenterJerusalem, Israel, Israel

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