Removal of Anti-Angiogenic Proteins in Preeclampsia Before Delivery

The primary objective of this trial is to determine whether short-term apheresis using a
dextran sulfate adsorption (DSA) column (Liposorber LA-15 System; the Device) leads to a
reduction in circulating sFLT-1 in the blood of women with pre-term preeclampsia.

The following secondary objectives are aimed at evaluating the efficacy and safety of the
Device as well as the impact of removing circulating sFlt-1 on maternal and neonatal
outcomes:

1. To determine whether short-term apheresis using the Device in women with pre-term
preeclampsia leads to:

- a prolongation of pregnancy (ie, gestational age)

- a reduction in blood pressure (BP) and proteinuria

- an increase in fetal birth weight

2. To determine the safety of reducing maternal sFlt-1 levels using the Device.

Up to 16 patients will be enrolled. Initially, 4 patients will undergo apheresis UP TO 2
times in the first week and undergo all protocol-related assessments including PK of sFlt-1
levels. Based on an assessment of clinical response by the Investigator, these first 4
patients will be offered the option to continue apheresis treatments (without
pharmacokinetic [PK] assessments) up to twice weekly until delivery or until 34 weeks
gestation, whichever comes first. Following complete review of all parameters and outcomes
by an independent Data Safety Monitoring Board (DSMB), up to 12 additional patients will be
enrolled (total of up to 16).

UPDATE: The DSMB reviewed data after the first 4 patients and again after 10
patients/delivered infants had been treated. In the next 6 patients, DSMB review will occur
after every 3 patients/delivered infants. These remaining 6 patients may undergo apheresis
up to 3 times per week.

Inclusion Criteria (maternal):

1. Signed informed consent in a pregnant woman ages 18 and 45 years hospitalized for
pre-term preeclampsia

2. Pre-term preeclampsia defined by systolic BP ≥140 mm Hg or ≥90 mm Hg diastolic at or
after 23 weeks of gestation or at or before 32 weeks in gestation in a woman with
previously normal BP and proteinuria 0.3 grams in a 24-hour specimen or urine
protein/creatinine ratio >0.30.

3. sFlt-1/PlGF ratio >85 (blood levels of sFlt-1 and PlGF determined using CE-approved
Roche Diagnostics assays).

Exclusion Criteria (Maternal and Fetal):

Maternal:

1. Taking any form of angiotensin cascade blocker

2. History or diagnosis of pre-existing chronic hypertension (first 3 patients only)

3. History of cardiac impairments including uncontrolled arrhythmia, unstable angina,
decompensated congestive heart failure or valvular disease

4. History or diagnosis of chronic renal disease

5. Patients receiving anticoagulation therapy prior to study entry

6. Anticipated immediate delivery within 24 hours

7. Signs of central nervous system (CNS) dysfunction, including seizures, cerebral edema
(CT-scan or MRI)

8. History of thyroid disease

9. History of liver abnormalities

10. Pulmonary edema

11. Thrombocytopenia (platelet count < 100,000/mm3)

12. Anemia - hemoglobin < 8 g/dL

13. Evidence of "reverse Doppler" flow on umbilical Doppler

14. Placenta previa

15. Placental abruption

16. Pre-term labor

17. Active hepatitis B, C, or tuberculosis infection or HIV positive status

18. Any condition that the investigator deems a risk to the patient or fetus in
completing the study.

19. Any condition which in the opinion of the investigator would necessitate delivery in
the next 24 hours

Fetal characteristic that would exclude the mother from participating:

1. Trisomy

2. Biophysical profile (BPP) < 6

3. Amniotic fluid index (AFI) < 5 cm

4. Estimated fetal weight (EFW) < 5th percentile for gestational age (IUGR)