A Feasibility Study to Evaluate the Safety of the KNP-1000 Apheresis System in Severe Preeclampsia

NCT ID: NCT06580405

Last Updated: 2025-03-05

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 13 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-05-31
• Study Completion Date: 2028-06-30

Brief Summary

The study will primarily evaluate safety of the KNP-1000 apheresis system for pregnant women and their fetuses diagnosed with preeclampsia with severe features between 23- and 32-weeks' gestation (very preterm).

Conditions

Pre-Eclampsia, Severe

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

KNP-1000 Apheresis System

Participants are to be treated with the system up to 2 times per week, continuing through delivery or 34 weeks of pregnancy, whichever comes first.

Group Type: EXPERIMENTAL

KNP-1000 Apheresis System

Intervention Type: DEVICE

sFlt-1 is removed from the participants' plasma through treatment.

Interventions

KNP-1000 Apheresis System

sFlt-1 is removed from the participants' plasma through treatment.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

A participant is deemed suitable for inclusion in the investigation if she meets the following criteria:

1. Pregnant woman ≥ 23 0/7 and < 32 0/7 weeks gestation, aged 18 to 45 years, hospitalized for preeclampsia at time of enrollment.

2. Severe hypertension ever defined by resting systolic BP ≥ 160 mm Hg and/or diastolic BP ≥ 110 mm Hg on two occasions measured at least 4 hours apart.

3. Proteinuria, defined as ≥ 300 mg protein in a 24-hour urine collection or ≥ 0.3 protein/creatinine ratio.

4. Provision of signed and dated informed consent form.

Exclusion Criteria

A participant will be excluded from the investigation if any of the following maternal or fetal criteria are met.

1. Documented history of chronic hypertension, defined as systolic BP ≥ 140mmHg and/or systolic BP ≥ 90 mmHg before pregnancy or prior to 20 weeks of gestation.

2. Documented history of proteinuria prior to pregnancy or prior to 20 weeks of gestation.

3. Taking any form of angiotensin cascade blocker or angiotensin-converting enzyme (ACE) inhibitor at time of enrollment.

4. Documented history of cardiac impairments including uncontrolled arrhythmia, unstable angina, decompensated congestive heart failure, or valvular disease.

5. Actively receiving therapeutic anticoagulation therapy or within the therapeutic window after ceasing anticoagulation therapy at the time of enrollment.

6. Any condition which, in the opinion of the Investigator, would necessitate immediate delivery within 24 hours.

7. Signs or history of cerebral nervous system dysfunction, including seizures, cerebral edema (previously confirmed by computed tomography scan or magnetic resonance imaging per medical records).

8. Confirmed or suspected diagnosis of pulmonary edema at time of enrollment.

9. Diagnosis of HELLP syndrome.

10. Thrombocytopenia (platelet count < 100,000/mm3) at time of enrollment.

11. Anemia defined as hemoglobin < 8 g/dL at time of enrollment.

12. Absent or reverse flow on umbilical Doppler ultrasound exam at the time of screening, or documented history of negative or reverse flow during the current gestation period.

13. Diagnosis of placenta previa during the current gestation period.

14. Preterm labor at or before time of screening.

15. Documented medical history of active hepatitis B virus, hepatitis C virus (HCV), syphilis, tuberculosis infection, or human immunodeficiency virus (HIV) positive status.

16. Any condition that the Investigator deems a risk to the study participant or fetus in completing the investigation.

17. Hypersensitivity to dextran sulfate cellulose or heparin.

18. Multiple gestation.

19. Documented history of familial hypercholesterolemia.

20. Suspicion or diagnosis of placental abruption during the current gestation.

21. Patients who have received the drug treatment not recommended by the American College of Obstetricians and Gynecologists (ACOG) practice bulletin Gestational Hypertension and Preeclampsia (the clinical management guidelines) within 6 months prior to enrollment.

22. Patients who have participated in another clinical trial within 6 months prior to enrollment.

1. Documented record of chromosomal anomalies.

2. Identifiable structural fetal abnormalities present at time of screening or a record of such abnormalities prior to enrollment.

3. Oligohydramnios, defined as Amniotic fluid index (AFI) less than 5 cm when measured using the four-quadrant method at time of enrollment.

4. Fetal growth restriction (FGR) defined as estimated fetal weight (EFW) below the 5th percentile for gestational age.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 45 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Kaneka Medical America LLC

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Central Contacts

Takashi Shimai

Role: CONTACT

Takashi.Shimai@kaneka.com

5105988423

Takuji Nishide

Role: CONTACT

Takuji.Nishide@kaneka.com

5102030212

Other Identifiers

KNP-1000-US01

Identifier Type: -

Identifier Source: org_study_id