Pre-Eclampsia
Recent clinical, regulatory, research and industry developments relating to this disease.
Maternal hepatic immunology during pregnancy.
Pre-eclampsia: pathophysiology and clinical implications.
Preeclampsia: Pathophysiology, Challenges, and Perspectives
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
- 4 clinical trials expected to report results, the earliest in Q3 2028.
- Q3 2028A Randomized, Placebo-controlled Trial of DAPAgliflozin for Cardiovascular Risk Reduction in the Postpartum Period of Hypertensive Pregnancies
- Q3 2028Aspirin for the Prevention of Preeclampsia and Pregnancy Outcomes in Nulliparous Women After Assisted Reproductive Technology. APPART
- Q1 2029Chronic Hypertension and Acetyl Salicylic Acid in Pregnancy, a Multicenter Prospective Randomized Double-blind Placebo-controlled Trial.
- Q2 2029APPLE: Aspirin to Prevent Pregnancy Loss and Preeclampsia
Clinical MilestonesViewHide
- 2026-06-12Chronic Hypertension and Acetyl Salicylic Acid in Pregnancy, a Multicenter Prospective Randomized Double-blind Placebo-controlled Trial.Results expected Q1 2029
- 2026-05-07Aspirin for the Prevention of Preeclampsia and Pregnancy Outcomes in Nulliparous Women After Assisted Reproductive Technology. APPARTResults expected Q3 2028
- 2026-03-04A Randomized, Placebo-controlled Trial of DAPAgliflozin for Cardiovascular Risk Reduction in the Postpartum Period of Hypertensive PregnanciesResults expected Q3 2028
- 2026-01-20APPLE: Aspirin to Prevent Pregnancy Loss and PreeclampsiaResults expected Q2 2029
- 2026-06-12ClinicalChronic Hypertension and Acetyl Salicylic Acid in Pregnancy, a Multicenter Prospective Randomized Double-blind Placebo-controlled Trial.Results expected Q1 2029
- 2026-05-07ClinicalAspirin for the Prevention of Preeclampsia and Pregnancy Outcomes in Nulliparous Women After Assisted Reproductive Technology. APPARTResults expected Q3 2028
- 2026-03-04ClinicalA Randomized, Placebo-controlled Trial of DAPAgliflozin for Cardiovascular Risk Reduction in the Postpartum Period of Hypertensive PregnanciesResults expected Q3 2028
- 2026-02-08ClinicalRole of Vitamin D in Prevention of Preeclampsia Recurrence in Pregnant Women With Previous History of Preeclampsia: A Randomized Controlled TrialPrimary completion
- 2026-01-20ClinicalAPPLE: Aspirin to Prevent Pregnancy Loss and PreeclampsiaResults expected Q2 2029
Clinical trials
The current development programme across all trial phases.
Research activity
Key research shaping understanding of this disease, combining the latest publications with the most influential evidence.
Major themes8
- Pre-Eclampsia4
- Blood Pressure1
- Cholestasis, Intrahepatic1
- Decidua1
- Eclampsia1
- Fatty Liver1
- Gastrointestinal Microbiome1
- Hyperemesis Gravidarum1
Leading journals4
- Frontiers in immunology3
- BMC medicine1
- BMJ (Clinical research ed.)1
- Circulation research1
Leading researchers8
- Bai X1
- Burton GJ1
- Chen G1
- Degrelle S1
- Ding J1
- Fan D1
- Fang H1
- Fournier T1
Affiliations (unnormalised)6
- Affiliated Foshan Maternity & Child Healthcare Hospital1
- Beth Israel Deaconess Medical Center and Harvard Medical School1
- Cedars-Sinai Medical Center1
- Centre for Trophoblast Research1
- Foshan Fetal Medicine Research Institute1
- Harvard Medical School1
Disease profile
A grounded synthesis of the condition — overview, causes, mechanism, risk factors and current standard of care.
Pre-eclampsia is a complication of pregnancy marked by maternal hypertension and proteinuria, with or without edema. It usually appears after 20 weeks of gestation, most often in the third trimester, and can range from mild to severe. In some cases it may occur earlier in the setting of trophoblastic disease.
The cause of pre-eclampsia is not settled. The supplied literature points to the placenta as central to its development, with abnormal placentation and stress of the syncytiotrophoblast leading to release of soluble placental factors. Early-onset disease is linked to defective placentation, while late-onset disease may involve interactions between placental aging and maternal genetic predisposition to cardiovascular and metabolic disease.
The disease is described as a placental disorder that produces systemic maternal signs through soluble factors released from the placenta. Reviews highlight antiangiogenic placental factors such as sFLT1 and abnormal placentation as key mechanisms, with placental-uterine interactions in early pregnancy also emphasized. The literature also notes immunologic and metabolic contributions, including maternal hepatic immunologic adaptation during pregnancy.
First pregnancy is specifically noted as a common setting for pre-eclampsia. The literature also supports maternal genetic predisposition, particularly to cardiovascular and metabolic disease, as a risk factor for late-onset disease. Epidemiologic and immunologic aspects are covered in the grounding, but no additional specific risk factors are supported here.
The supplied grounding does not provide a treatment guideline or specific standard-of-care regimen. It indicates that management is challenging because treatment affects both mother and fetus, but it does not support a particular modality or drug class. No treatment categories can be stated from the provided material.
AI-generated summary grounded in MeSH and 4 peer-reviewed sources. Informational only — not medical advice. Generated 2026-07-07.
Reference
Authoritative identity, definition & identifiers.
A complication of PREGNANCY, characterized by a complex of symptoms including maternal HYPERTENSION and PROTEINURIA with or without pathological EDEMA. Symptoms may range between mild and severe. Pre-eclampsia usually occurs after the 20th week of gestation, but may develop before this time in the presence of trophoblastic disease.
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Clinical trials — ClinicalTrials.gov (U.S. National Library of Medicine)
- Research activity — Europe PMC (EMBL-EBI) + OpenAlex-derived paper links
- Related entities are derived from literature co-mention (studied together) — associative, not causal.