Preeclampsia (PE)Phase 1/2NCT07738562
Dipyridamole for Early-Onset Preeclampsia: A Pilot Study of Feasibility, Pharmacokinetics, and Biological Effects
A Phase 1/2 study testing Dipyridamole 75 MG in people with Preeclampsia (PE) and Hypertension ,Pregnancy, run by Hadassah Medical Organization at 1 site in Israel.
Trial summary
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. Read more about this study
- Who is it for?
- Ages 18 years and older, women only
- Conditions the study is for
- Preeclampsia (PE), Hypertension ,Pregnancy
- What is being tested?
- Dipyridamole 75 MG
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 15 participants
- Where
- 1 siteIsrael
- Study dates
- Sep 2026to Sep 2028
- Phase
- Phase 1/2
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- Women only
- No healthy volunteers
- Adult, Older adult
Who may be able to join
None listed.
Who cannot join
- Immediate indication for delivery at time of screening, including uncontrolled severe hypertension, eclampsia, HELLP syndrome, or severe fetal compromise
- Active maternal bleeding or clinically significant bleeding disorder
- Therapeutic-dose anticoagulation (e.g., enoxaparin >1 mg/kg/day)
- Known hypersensitivity or contraindication to dipyridamole
- Multiple gestation
- Known major fetal anomaly or chromosomal abnormality
Show all 10Show fewer
- Baseline thrombocytopenia, platelet count <100,000/µL
- Hemodynamically significant maternal cardiac disease
- Significant maternal comorbidity that, in the investigator's judgment, precludes safe participation
- Inability to comply with study procedures
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
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.
Read more
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 with safety gates reviewed by an independent Safety Monitoring Committee. Participants receive oral dipyridamole added to standard clinical care, using a fixed dose-escalation protocol (75 mg twice daily on Day 1, escalating over 2-3 days to a target dose of 75 mg four times daily, 300 mg/day total). Standard obstetric care continues unchanged, determined entirely on clinical grounds, independent of study participation.
The primary objective is to evaluate the feasibility and clinical implementability of the dipyridamole treatment protocol within routine inpatient obstetric care. Secondary objectives include characterizing the pharmacokinetics of dipyridamole during pregnancy, assessing tolerability, and evaluating longitudinal circulating angiogenic biomarkers (sFlt-1 and PlGF). Exploratory objectives include assessment of placental markers of oxidative stress and ferroptosis-related pathways in tissue obtained at delivery.
Study drug is administered during the antepartum period only and discontinued before delivery. This pilot study is not designed to establish clinical efficacy, but to provide the pharmacokinetic, tolerability, and biological data required to design a subsequent randomized trial.
Read the detailed description
Study Type: Single-center, open-label, pilot interventional study evaluating an approved medication (dipyridamole) in an off-label indication.
Background and Rationale:
Early-onset preeclampsia (PE), typically presenting before 34 weeks of gestation, is the most severe phenotype of hypertensive pregnancy disease and a leading cause of maternal and perinatal morbidity. Once clinically established, there is no disease-modifying therapy; management relies almost exclusively on close surveillance and timely delivery, frequently resulting in extreme prematurity. Early-onset PE is increasingly recognized as a primarily placental disorder, driven by defective placentation, chronic ischemia-reperfusion injury, progressive trophoblast damage, and maladaptive stress responses, in contrast to late-onset disease, which is more strongly influenced by maternal cardiovascular and metabolic susceptibility.
Prior laboratory research identified ferroptosis, a form of regulated cell death driven by iron-catalyzed peroxidation of membrane phospholipids, as a key mechanism of placental injury in early-onset PE. Human trophoblasts were shown to be uniquely vulnerable to ferroptosis due to their high iron content and intense oxidative metabolism. Using redox phospholipidomics, preeclamptic placentas were shown to accumulate specific hydroperoxy-phosphatidylethanolamine species characteristic of ferroptotic cell death; inducing ferroptosis in placental explants drove sFlt-1 release, and ferroptosis inhibitors reversed both tissue damage and sFlt-1 secretion. Multiple independent groups have since confirmed ferroptosis as a driver of placental injury in preeclampsia.
A high-throughput robotic screen of over 6,500 drugs and compounds, designed to identify pregnancy-safe ferroptosis inhibitors in primary human trophoblast cultures, identified dipyridamole as one of the most potent candidates (EC50 = 0.146 μM), acting independently of its known phosphodiesterase-inhibitory pharmacology. In preeclamptic placental explants, dipyridamole treatment led to a marked and reproducible reduction in sFlt-1 release, a central pathogenic mediator of the maternal syndrome.
From a safety perspective, dipyridamole has an established pregnancy safety record. It is classified as FDA Pregnancy Category B, and a Cochrane meta-analysis of antiplatelet agents in pregnancy confirmed that this drug class is safe and reduces preeclampsia, preterm birth, and small-for-gestational-age births.
Study Rationale Summary:
This study combines a defined molecular target (ferroptosis) with circulating biomarkers (sFlt-1/PlGF ratio) and Doppler parameters that can objectively track placental stress and treatment response, in a population with biomarker-confirmed placental dysfunction expected to deteriorate without intervention. If successful, this pilot would provide preliminary evidence supporting further evaluation of a disease-modifying therapy for established early-onset preeclampsia.
Study Design:
This is a prospective, single-center, open-label pilot study using a sequential, fixed dose-escalation design, evaluating the feasibility and clinical implementation of dipyridamole treatment in women with early-onset preeclampsia, including pharmacokinetic assessment, within standard obstetric care. The study is intentionally designed as a non-randomized pilot; its purpose is not to establish definitive clinical efficacy, but to assess real-world implementability, characterize pharmacokinetics and tolerability during pregnancy, and generate biological and clinical signals to inform the design of a subsequent randomized controlled trial.
Enrollment proceeds through a staged sentinel design: the first participant is enrolled and treated alone, with no further enrollment until she has completed treatment, delivered, and been assessed through the first 24 hours postpartum, and until the independent Safety Monitoring Committee has reviewed the complete safety data and recommended proceeding. Following a favorable review, two additional participants are enrolled, with a second safety gate before enrollment continues toward the planned sample size. This staged approach allows accumulated safety experience to govern each expansion of exposure.
All participants receive dipyridamole in addition to standard clinical management for early-onset preeclampsia, provided in accordance with established international and national guidelines. Study participation does not modify, delay, or replace any component of standard clinical care; decisions regarding antihypertensive therapy, treatment escalation, or delivery timing are made exclusively on clinical grounds by the treating team, independent of study participation. The dose-escalation scheme is fixed and identical for all participants; dosing is not individualized and accelerated escalation is not permitted.
Pharmacokinetic Sampling:
Pharmacokinetic blood samples are drawn, whenever possible, from the participant's existing indwelling intravenous catheter to minimize discomfort. Sparse sampling is performed during the dose-escalation phase, and after reaching the target dose each participant undergoes one intensive pharmacokinetic profiling day, provided maternal and fetal conditions allow a stable sampling window.
Safety Oversight:
Safety oversight is provided by an independent Safety Monitoring Committee comprising five members: an external maternal-fetal medicine specialist, a neonatologist, a hematologist with expertise in coagulation and bleeding risk, a specialist in internal medicine and clinical pharmacology, and an independent epidemiologist/biostatistician. The Committee is independent of the conduct of the study and reviews all serious adverse events, all events meeting a stopping-rule trigger, and cumulative safety data. It governs the staged sentinel enrollment gates and conducts scheduled safety reviews after the first 5 and first 10 participants complete treatment, in addition to any ad hoc reviews triggered by safety events. Final clinical decisions remain with the treating team, with maternal and fetal safety taking priority.
Postpartum follow-up continues to six weeks and includes documentation of adverse events, blood pressure and antihypertensive requirement, readmission, postpartum hemorrhage, infection or surgical complication, and hemoglobin.
- Conditions
- Preeclampsia (PE), Hypertension ,Pregnancy
- Being tested
- Dipyridamole 75 MG
- Keywords
- Preeclampsia treatment, preeclampsia management, treating mild preeclampsia, Early-onset preeclampsia, hypertensive pregnancy disease, preeclampsia disease-modifying therapy
- Medical subject headings
- Pre-Eclampsia, Hypertension, Pregnancy-Induced
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Dipyridamole 75 MGDrug
Oral dipyridamole 75 mg tablets, administered via a fixed structured dose escalation across the sequential arms described above (75 mg twice daily → three times daily → four times daily). The escalation schedule is identical for all participants; dosing is not individualized and accelerated escalation is not permitted.
| Study group | Role | What they receive |
|---|---|---|
| Dipyridamole 75 mg twice daily (Day 1) | Experimental | Initial fixed dose-escalation step. All participants receive oral dipyridamole 75 mg twice daily on Day 1, with clinical monitoring for tolerability prior to escalation to the next dose level. Receives: Drug: Dipyridamole 75 MG |
| Dipyridamole 75 mg three times daily (Day 2) | Experimental | Second fixed dose-escalation step. Participants who tolerate the initial dose escalate to dipyridamole 75 mg three times daily on Day 2. The escalation schedule is fixed and identical for all participants; dosing is not individualized and accelerated escalation is not permitted. Receives: Drug: Dipyridamole 75 MG |
| Dipyridamole 75 mg four times daily (target dose, Day 3 onward) | Experimental | Target maintenance dose. Participants escalate to dipyridamole 75 mg four times daily (300 mg/day total) from Day 3 onward, continuing throughout the antepartum period. Study drug is discontinued at least 12 hours before planned delivery, and at least 24 hours before planned delivery at which neuraxial anesthesia is anticipated. Temporary hold or de-escalation to a previously tolerated dose level is permitted based on adverse effects or investigator judgment. Receives: Drug: Dipyridamole 75 MG |
What is being measured
The primary outcome is the main question the study is designed to answer.
Protocol Feasibility
Composite feasibility endpoint defined as: (1) successful enrollment of ≥10 of 15 planned participants within the recruitment period; (2) completion of the full dose-escalation ramp-up to the target dose of 300 mg/day in ≥70% of enrolled participants; and (3) successful collection of at least the sparse pharmacokinetic sampling set (Day 1 pre-dose + 2 post-dose samples) in ≥70% of participants, within the routine inpatient care setting.
Measured: From enrollment through delivery (estimated 1-5 weeks per participant)
Secondary outcomes (17)
Peak Plasma Concentration (Cmax) of Dipyridamole
Maximum observed plasma concentration of dipyridamole, estimated from sparse sampling during dose escalation and intensive PK profiling
Measured: Pre-dose through 6-8 hours post-dose on the intensive PK profiling day (after reaching target dose or highest tolerated dose)
Incidence of Dipyridamole-Related Adverse Events
Number and proportion of participants experiencing adverse events attributed to dipyridamole during the ramp-up and maintenance dosing period (per your protocol's documented AE categories: dizziness, headache, rash, abdominal distress, bleeding). Unit: Number of participants
Measured: From first drug administration until six weeks postpartum
Change in Serum Soluble fms-Like Tyrosine Kinase-1 (sFlt-1)
Longitudinal change in maternal circulating sFlt-1 concentration following dipyridamole treatment initiation. Unit: pg/mL
Measured: Daily for the first 7 days, then every 72 hours until delivery
Change in Maternal Blood Pressure
Systolic and diastolic blood pressure trends from treatment initiation to delivery
Measured: From treatment initiation until delivery (estimated 1-5 weeks)
Pregnancy Latency from Treatment Initiation to Delivery
Number of days from first dose of dipyridamole to delivery, as a measure of the clinical disease trajectory under treatment. unit- days
Measured: From first dose through delivery (estimated 1-5 weeks)
Uterine Artery Pulsatility Index (UtA-PI)
Serial assessment of uterine artery pulsatility index, measured at baseline and at least twice weekly during treatment, as a measurable indicator of placental vascular resistance and response to treatment. Resistance index (unitless ratio)
Measured: From enrollment through delivery (estimated 1-5 weeks)
Trough Plasma Concentration (Ctrough) of Dipyridamole
Pre-dose plasma concentration measured at steady state during dose escalation and maintenance dosing
Measured: From treatment initiation through delivery (estimated 1-5 weeks)
Area Under the Plasma Concentration-Time Curve (AUC) of Dipyridamole
Total systemic exposure to dipyridamole, calculated from the concentration-time profile obtained on the intensive PK profiling day
Measured: Pre-dose through 6-8 hours post-dose on the intensive PK profiling day
Apparent Oral Clearance (CL/F) of Dipyridamole
Apparent clearance estimated from plasma concentration data using population or non-compartmental PK modeling
Measured: From treatment initiation through the intensive PK profiling day (estimated 1-5 weeks)
Terminal Elimination Half-Life (t½) of Dipyridamole
Time required for plasma dipyridamole concentration to decrease by half, estimated from the terminal phase of the concentration-time curve
Measured: Calculated from PK samples collected on the intensive PK profiling day (up to 6-8 hours post-dose)
Need for Initiation or Escalation of Antihypertensive Therapy
Proportion of participants requiring new initiation or dose escalation of antihypertensive medication after treatment start
Measured: From treatment initiation until delivery (estimated 1-5 weeks)
Overall Antihypertensive Medication Burden
Cumulative antihypertensive drug exposure (e.g., number of agents and/or total dose) during treatment
Measured: From treatment initiation until delivery (estimated 1-5 weeks)
Change in Serum Placental Growth Factor (PlGF)
Longitudinal change in maternal circulating PlGF concentration following dipyridamole treatment initiation. Unit: pg/mL
Measured: Daily for the first 7 days, then every 72 hours until delivery
Change in sFlt-1/PlGF Ratio
Longitudinal change in the sFlt-1/PlGF ratio, a composite marker of angiogenic imbalance in placental dysfunction
Measured: Daily for the first 7 days, then every 72 hours until delivery
Severity of Dipyridamole-Related Adverse Events
Distribution of adverse event severity grades among participants experiencing dipyridamole-related adverse effects Unit: Number of participants (by severity category - e.g., mild/moderate/severe, or CTCAE grade if you're grading formally)
Measured: From first drug administration until six weeks postpartum
Obstetric Indication for Delivery
Primary clinical reason/indication for delivery, documented for each participant. Number of participants (by indication category)
Measured: At delivery
Umbilical Artery Pulsatility Index (UA-PI)
Serial assessment of umbilical artery pulsatility index, measured at baseline and at least twice weekly during treatment, as a measurable indicator of placental vascular resistance and fetal-placental circulation. Resistance index (unitless ratio)
Measured: From enrollment through delivery (estimated 1-5 weeks)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted31 Jul 2026
- Study startSep 2026 (estimated)
- Primary completionSep 2028 (estimated)
- Study completionSep 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (9)Papers the sponsor has linked to this study.
- Other trials for Preeclampsia (PE)Studies of the same condition, open and under way.
- More trials run by Hadassah Medical OrganizationThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 1/2
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Sequential
- Masking
- None (open label)
- Enrolment
- 15 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Hadassah Medical Organization
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Bahrir Ofer, Hadassah Medical Organization
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07738562
- Sponsor's protocol ID
- Dipyridamole
- Status last verified
- Jul 2026
- First submitted
- 23 May 2026
- Last updated
- 31 Jul 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Chen X, Shen J, Jiang X, Pan M, Chang S, Li J, Wang L, Miao M, Feng X, Zhang L, Shu G, Liu W, Xu F, Zhang W, Ding Z, Zong H, Liu W, Li D, Chen B, Shao M, Fei G, Zha X, Fan X. Characterization of dipyridamole as a novel ferroptosis inhibitor and its therapeutic potential in acute respiratory distress syndrome management. Theranostics. 2024 Oct 21;14(18):6947-6968. doi: 10.7150/thno.102318. eCollection 2024.
PubMed 39629132Zhuang X, Shi S, Liu S, Jiao Y, Huang B, Yang Y, Yang L, Yang X, Wang H, Liang C, Song D, Yu H, Zou D, Sun Q, Yang S, Yin C, Li J, Liu Y, Min J, Wang F, Nian Y, Du L, Chu B. Dipyridamole Acts as Clinical Ferroptosis Inhibitor to Prevent from Tissue Injury. Adv Sci (Weinh). 2025 Jun;12(23):e2500566. doi: 10.1002/advs.202500566. Epub 2025 May 14.
PubMed 40365742Edri T, Lianski S, Cohen SM, Beharier O. Placental ferroptosis in preeclampsia: An integrative and comprehensive review. J Reprod Immunol. 2026 Mar;174:104863. doi: 10.1016/j.jri.2026.104863. Epub 2026 Feb 16.
PubMed 41722450Uzan S, Beaufils M, Breart G, Bazin B, Capitant C, Paris J. Prevention of fetal growth retardation with low-dose aspirin: findings of the EPREDA trial. Lancet. 1991 Jun 15;337(8755):1427-31. doi: 10.1016/0140-6736(91)93124-r.
PubMed 1675315Beaufils M, Uzan S, Donsimoni R, Colau JC. Prevention of pre-eclampsia by early antiplatelet therapy. Lancet. 1985 Apr 13;1(8433):840-2. doi: 10.1016/s0140-6736(85)92207-x.
PubMed 2858710Gestational Hypertension and Preeclampsia: ACOG Practice Bulletin, Number 222. Obstet Gynecol. 2020 Jun;135(6):e237-e260. doi: 10.1097/AOG.0000000000003891.
PubMed 32443079ESPRIT Study Group; Halkes PH, van Gijn J, Kappelle LJ, Koudstaal PJ, Algra A. Aspirin plus dipyridamole versus aspirin alone after cerebral ischaemia of arterial origin (ESPRIT): randomised controlled trial. Lancet. 2006 May 20;367(9523):1665-73. doi: 10.1016/S0140-6736(06)68734-5.
PubMed 16714187Park C, Alahari S, Ausman J, Liu R, Nguyen F, Sallais J, Post M, Caniggia I. Placental Hypoxia-Induced Ferroptosis Drives Vascular Damage in Preeclampsia. Circ Res. 2025 Feb 14;136(4):361-378. doi: 10.1161/CIRCRESAHA.124.325119. Epub 2025 Jan 23.
PubMed 39846172Lianski S, Mizrachi T, Barak O, Tsaitlin-Mor L, Elhaik-Goldman S, Yagel S, Goldman-Wohl D, Cohen SM, Hefetz Medina R, Rachmilewitz J, Barr HM, Plotnikov A, Tyurina YY, Tyurin VA, Samovich SN, Kapralov AA, Karumanchi SA, Kagan VE, Bayir H, Sadovsky Y, Beharier O. Antiferroptotic Drugs Reduce sFlt-1 Release and Placenta Damage in Preeclampsia. Hypertension. 2025 Oct;82(10):1705-1718. doi: 10.1161/HYPERTENSIONAHA.125.25003. Epub 2025 Aug 19.
PubMed 40827397
Study at a glance
From the registry record, last updated by the sponsor on 31 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Dipyridamole for Early-Onset Preeclampsia: A Pilot Study of Feasibility, Pharmacokinetics, and Biological Effects
- ClinicalTrials.gov ID
- NCT07738562
- Acronym / sponsor ID
- Dipyridamole
- Conditions
- Preeclampsia (PE), Hypertension ,Pregnancy
- Keywords
- Preeclampsia treatment, preeclampsia management, treating mild preeclampsia, Early-onset preeclampsia, hypertensive pregnancy disease, preeclampsia disease-modifying therapy
- Phase
- Phase 1/2
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 15 participants (estimated)
- Lead sponsor
- Hadassah Medical OrganizationUniversity, hospital or other
- Study start
- Sep 2026 (estimated)
- Primary completion
- Sep 2028 (estimated)
- Study completion
- Sep 2028 (estimated)
- First posted
- 31 Jul 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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 with safety gates reviewed by an independent Safety Monitoring Committee. Participants receive oral dipyridamole added to standard clinical care, using a fixed dose-escalation protocol (75 mg twice daily on Day 1, escalating over 2-3 days to a target dose of 75 mg four times daily, 300 mg/day total). Standard obstetric care continues unchanged, determined entirely on clinical grounds, independent of study participation.
The primary objective is to evaluate the feasibility and clinical implementability of the dipyridamole treatment protocol within routine inpatient obstetric care. Secondary objectives include characterizing the pharmacokinetics of dipyridamole during pregnancy, assessing tolerability, and evaluating longitudinal circulating angiogenic biomarkers (sFlt-1 and PlGF). Exploratory objectives include assessment of placental markers of oxidative stress and ferroptosis-related pathways in tissue obtained at delivery.
Study drug is administered during the antepartum period only and discontinued before delivery. This pilot study is not designed to establish clinical efficacy, but to provide the pharmacokinetic, tolerability, and biological data required to design a subsequent randomized trial.
Detailed description
Study Type: Single-center, open-label, pilot interventional study evaluating an approved medication (dipyridamole) in an off-label indication.
Background and Rationale:
Early-onset preeclampsia (PE), typically presenting before 34 weeks of gestation, is the most severe phenotype of hypertensive pregnancy disease and a leading cause of maternal and perinatal morbidity. Once clinically established, there is no disease-modifying therapy; management relies almost exclusively on close surveillance and timely delivery, frequently resulting in extreme prematurity. Early-onset PE is increasingly recognized as a primarily placental disorder, driven by defective placentation, chronic ischemia-reperfusion injury, progressive trophoblast damage, and maladaptive stress responses, in contrast to late-onset disease, which is more strongly influenced by maternal cardiovascular and metabolic susceptibility.
Prior laboratory research identified ferroptosis, a form of regulated cell death driven by iron-catalyzed peroxidation of membrane phospholipids, as a key mechanism of placental injury in early-onset PE. Human trophoblasts were shown to be uniquely vulnerable to ferroptosis due to their high iron content and intense oxidative metabolism. Using redox phospholipidomics, preeclamptic placentas were shown to accumulate specific hydroperoxy-phosphatidylethanolamine species characteristic of ferroptotic cell death; inducing ferroptosis in placental explants drove sFlt-1 release, and ferroptosis inhibitors reversed both tissue damage and sFlt-1 secretion. Multiple independent groups have since confirmed ferroptosis as a driver of placental injury in preeclampsia.
A high-throughput robotic screen of over 6,500 drugs and compounds, designed to identify pregnancy-safe ferroptosis inhibitors in primary human trophoblast cultures, identified dipyridamole as one of the most potent candidates (EC50 = 0.146 μM), acting independently of its known phosphodiesterase-inhibitory pharmacology. In preeclamptic placental explants, dipyridamole treatment led to a marked and reproducible reduction in sFlt-1 release, a central pathogenic mediator of the maternal syndrome.
From a safety perspective, dipyridamole has an established pregnancy safety record. It is classified as FDA Pregnancy Category B, and a Cochrane meta-analysis of antiplatelet agents in pregnancy confirmed that this drug class is safe and reduces preeclampsia, preterm birth, and small-for-gestational-age births.
Study Rationale Summary:
This study combines a defined molecular target (ferroptosis) with circulating biomarkers (sFlt-1/PlGF ratio) and Doppler parameters that can objectively track placental stress and treatment response, in a population with biomarker-confirmed placental dysfunction expected to deteriorate without intervention. If successful, this pilot would provide preliminary evidence supporting further evaluation of a disease-modifying therapy for established early-onset preeclampsia.
Study Design:
This is a prospective, single-center, open-label pilot study using a sequential, fixed dose-escalation design, evaluating the feasibility and clinical implementation of dipyridamole treatment in women with early-onset preeclampsia, including pharmacokinetic assessment, within standard obstetric care. The study is intentionally designed as a non-randomized pilot; its purpose is not to establish definitive clinical efficacy, but to assess real-world implementability, characterize pharmacokinetics and tolerability during pregnancy, and generate biological and clinical signals to inform the design of a subsequent randomized controlled trial.
Enrollment proceeds through a staged sentinel design: the first participant is enrolled and treated alone, with no further enrollment until she has completed treatment, delivered, and been assessed through the first 24 hours postpartum, and until the independent Safety Monitoring Committee has reviewed the complete safety data and recommended proceeding. Following a favorable review, two additional participants are enrolled, with a second safety gate before enrollment continues toward the planned sample size. This staged approach allows accumulated safety experience to govern each expansion of exposure.
All participants receive dipyridamole in addition to standard clinical management for early-onset preeclampsia, provided in accordance with established international and national guidelines. Study participation does not modify, delay, or replace any component of standard clinical care; decisions regarding antihypertensive therapy, treatment escalation, or delivery timing are made exclusively on clinical grounds by the treating team, independent of study participation. The dose-escalation scheme is fixed and identical for all participants; dosing is not individualized and accelerated escalation is not permitted.
Pharmacokinetic Sampling:
Pharmacokinetic blood samples are drawn, whenever possible, from the participant's existing indwelling intravenous catheter to minimize discomfort. Sparse sampling is performed during the dose-escalation phase, and after reaching the target dose each participant undergoes one intensive pharmacokinetic profiling day, provided maternal and fetal conditions allow a stable sampling window.
Safety Oversight:
Safety oversight is provided by an independent Safety Monitoring Committee comprising five members: an external maternal-fetal medicine specialist, a neonatologist, a hematologist with expertise in coagulation and bleeding risk, a specialist in internal medicine and clinical pharmacology, and an independent epidemiologist/biostatistician. The Committee is independent of the conduct of the study and reviews all serious adverse events, all events meeting a stopping-rule trigger, and cumulative safety data. It governs the staged sentinel enrollment gates and conducts scheduled safety reviews after the first 5 and first 10 participants complete treatment, in addition to any ad hoc reviews triggered by safety events. Final clinical decisions remain with the treating team, with maternal and fetal safety taking priority.
Postpartum follow-up continues to six weeks and includes documentation of adverse events, blood pressure and antihypertensive requirement, readmission, postpartum hemorrhage, infection or surgical complication, and hemoglobin.
Study design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Sequential
- Masking
- None (open label)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Dipyridamole 75 mg twice daily (Day 1) | Experimental | Drug: Dipyridamole 75 MGInitial fixed dose-escalation step. All participants receive oral dipyridamole 75 mg twice daily on Day 1, with clinical monitoring for tolerability prior to escalation to the next dose level. |
| Dipyridamole 75 mg three times daily (Day 2) | Experimental | Drug: Dipyridamole 75 MGSecond fixed dose-escalation step. Participants who tolerate the initial dose escalate to dipyridamole 75 mg three times daily on Day 2. The escalation schedule is fixed and identical for all participants; dosing is not individualized and accelerated escalation is not permitted. |
| Dipyridamole 75 mg four times daily (target dose, Day 3 onward) | Experimental | Drug: Dipyridamole 75 MGTarget maintenance dose. Participants escalate to dipyridamole 75 mg four times daily (300 mg/day total) from Day 3 onward, continuing throughout the antepartum period. Study drug is discontinued at least 12 hours before planned delivery, and at least 24 hours before planned delivery at which neuraxial anesthesia is anticipated. Temporary hold or de-escalation to a previously tolerated dose level is permitted based on adverse effects or investigator judgment. |
Who may qualify
- Ages
- 18 years and older
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (0 listed)
Key exclusion criteria (10 listed)
- Immediate indication for delivery at time of screening, including uncontrolled severe hypertension, eclampsia, HELLP syndrome, or severe fetal compromise
- Active maternal bleeding or clinically significant bleeding disorder
- Therapeutic-dose anticoagulation (e.g., enoxaparin >1 mg/kg/day)
- Known hypersensitivity or contraindication to dipyridamole
- Multiple gestation
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Dipyridamole 75 MGOral dipyridamole 75 mg tablets, administered via a fixed structured dose escalation across the sequential arms described above (75 mg twice daily → three times daily → four times daily). The escalation schedule is identical for all participants; dosing is not individualized and accelerated escalation is not permitted. | Drug | Dipyridamole 75 mg four times daily (target dose, Day 3 onward), Dipyridamole 75 mg three times daily (Day 2), Dipyridamole 75 mg twice daily (Day 1) |
Primary outcome
Protocol Feasibility
Time frame: From enrollment through delivery (estimated 1-5 weeks per participant)
Composite feasibility endpoint defined as: (1) successful enrollment of ≥10 of 15 planned participants within the recruitment period; (2) completion of the full dose-escalation ramp-up to the target dose of 300 mg/day in ≥70% of enrolled participants; and (3) successful collection of at least the sparse pharmacokinetic sampling set (Day 1 pre-dose + 2 post-dose samples) in ≥70% of participants, within the routine inpatient care setting.
17 secondary outcomes
Peak Plasma Concentration (Cmax) of Dipyridamole
Time frame: Pre-dose through 6-8 hours post-dose on the intensive PK profiling day (after reaching target dose or highest tolerated dose)
Incidence of Dipyridamole-Related Adverse Events
Time frame: From first drug administration until six weeks postpartum
Change in Serum Soluble fms-Like Tyrosine Kinase-1 (sFlt-1)
Time frame: Daily for the first 7 days, then every 72 hours until delivery
Change in Maternal Blood Pressure
Time frame: From treatment initiation until delivery (estimated 1-5 weeks)
Pregnancy Latency from Treatment Initiation to Delivery
Time frame: From first dose through delivery (estimated 1-5 weeks)
Uterine Artery Pulsatility Index (UtA-PI)
Time frame: From enrollment through delivery (estimated 1-5 weeks)
Trough Plasma Concentration (Ctrough) of Dipyridamole
Time frame: From treatment initiation through delivery (estimated 1-5 weeks)
Area Under the Plasma Concentration-Time Curve (AUC) of Dipyridamole
Time frame: Pre-dose through 6-8 hours post-dose on the intensive PK profiling day
Apparent Oral Clearance (CL/F) of Dipyridamole
Time frame: From treatment initiation through the intensive PK profiling day (estimated 1-5 weeks)
Terminal Elimination Half-Life (t½) of Dipyridamole
Time frame: Calculated from PK samples collected on the intensive PK profiling day (up to 6-8 hours post-dose)
Need for Initiation or Escalation of Antihypertensive Therapy
Time frame: From treatment initiation until delivery (estimated 1-5 weeks)
Overall Antihypertensive Medication Burden
Time frame: From treatment initiation until delivery (estimated 1-5 weeks)
Change in Serum Placental Growth Factor (PlGF)
Time frame: Daily for the first 7 days, then every 72 hours until delivery
Change in sFlt-1/PlGF Ratio
Time frame: Daily for the first 7 days, then every 72 hours until delivery
Severity of Dipyridamole-Related Adverse Events
Time frame: From first drug administration until six weeks postpartum
Obstetric Indication for Delivery
Time frame: At delivery
Umbilical Artery Pulsatility Index (UA-PI)
Time frame: From enrollment through delivery (estimated 1-5 weeks)
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 31 Jul 2026.
- Background: PubMed 39629132Chen X, Shen J, Jiang X, Pan M, Chang S, Li J, Wang L, Miao M, Feng X, Zhang L, Shu G, Liu W, Xu F, Zhang W, Ding Z, Zong H, Liu W, Li D, Chen B, Shao M, Fei G, Zha X, Fan X. Characterization of dipyridamole as a novel ferroptosis inhibitor and its therapeutic potential in acute respiratory distress syndrome management. Theranostics. 2024 Oct 21;14(18):6947-6968. doi: 10.7150/thno.102318. eCollection 2024.
- Background: PubMed 40365742Zhuang X, Shi S, Liu S, Jiao Y, Huang B, Yang Y, Yang L, Yang X, Wang H, Liang C, Song D, Yu H, Zou D, Sun Q, Yang S, Yin C, Li J, Liu Y, Min J, Wang F, Nian Y, Du L, Chu B. Dipyridamole Acts as Clinical Ferroptosis Inhibitor to Prevent from Tissue Injury. Adv Sci (Weinh). 2025 Jun;12(23):e2500566. doi: 10.1002/advs.202500566. Epub 2025 May 14.
- Background: PubMed 41722450Edri T, Lianski S, Cohen SM, Beharier O. Placental ferroptosis in preeclampsia: An integrative and comprehensive review. J Reprod Immunol. 2026 Mar;174:104863. doi: 10.1016/j.jri.2026.104863. Epub 2026 Feb 16.
- Background: PubMed 1675315Uzan S, Beaufils M, Breart G, Bazin B, Capitant C, Paris J. Prevention of fetal growth retardation with low-dose aspirin: findings of the EPREDA trial. Lancet. 1991 Jun 15;337(8755):1427-31. doi: 10.1016/0140-6736(91)93124-r.
- Background: PubMed 2858710Beaufils M, Uzan S, Donsimoni R, Colau JC. Prevention of pre-eclampsia by early antiplatelet therapy. Lancet. 1985 Apr 13;1(8433):840-2. doi: 10.1016/s0140-6736(85)92207-x.
- Background: PubMed 32443079Gestational Hypertension and Preeclampsia: ACOG Practice Bulletin, Number 222. Obstet Gynecol. 2020 Jun;135(6):e237-e260. doi: 10.1097/AOG.0000000000003891.
- Background: PubMed 16714187ESPRIT Study Group; Halkes PH, van Gijn J, Kappelle LJ, Koudstaal PJ, Algra A. Aspirin plus dipyridamole versus aspirin alone after cerebral ischaemia of arterial origin (ESPRIT): randomised controlled trial. Lancet. 2006 May 20;367(9523):1665-73. doi: 10.1016/S0140-6736(06)68734-5.
- Background: PubMed 39846172Park C, Alahari S, Ausman J, Liu R, Nguyen F, Sallais J, Post M, Caniggia I. Placental Hypoxia-Induced Ferroptosis Drives Vascular Damage in Preeclampsia. Circ Res. 2025 Feb 14;136(4):361-378. doi: 10.1161/CIRCRESAHA.124.325119. Epub 2025 Jan 23.
- Background: PubMed 40827397Lianski S, Mizrachi T, Barak O, Tsaitlin-Mor L, Elhaik-Goldman S, Yagel S, Goldman-Wohl D, Cohen SM, Hefetz Medina R, Rachmilewitz J, Barr HM, Plotnikov A, Tyurina YY, Tyurin VA, Samovich SN, Kapralov AA, Karumanchi SA, Kagan VE, Bayir H, Sadovsky Y, Beharier O. Antiferroptotic Drugs Reduce sFlt-1 Release and Placenta Damage in Preeclampsia. Hypertension. 2025 Oct;82(10):1705-1718. doi: 10.1161/HYPERTENSIONAHA.125.25003. Epub 2025 Aug 19.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1/2 study testing Dipyridamole 75 MG in people with Preeclampsia (PE) and Hypertension ,Pregnancy, run by Hadassah Medical Organization at 1 site in Israel.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 0 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 31 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Israel. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this combined phase mean?
Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Prof. Ofer Beharier, Principal Investigator (972+586306700, bofer@hadassah.org.il), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Protocol Feasibility (time frame: From enrollment through delivery (estimated 1-5 weeks per participant)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07738562, which also lists 9 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 31 Jul 2026.