Skip to main content
Clinical Trials/EUCTR2018-002904-14-NL
EUCTR2018-002904-14-NLActive, not recruitingPhase 1

A Phase I/II, Open Label, Proof of Concept Study to investigate Tolerability and Safety of Treatment with Recombinant Human C1 Inhibitor in Patients with Preeclampsia. - Preeclampsia Study

Pharming Technologies B.V.0 sites30 target enrollmentStarted: October 4, 2018Last updated:
Conditions
Drugs

Trial Snapshot

Phase
Phase 1
Status
Active, not recruiting
Enrollment
30

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional clinical trial of medicinal product

Eligibility Criteria

Inclusion Criteria

  • 1. Pregnant females, aged = 18 years
  • 2. Singleton pregnancy
  • 3. Between 25 and 35 weeks of gestation
  • 4. Diagnosis of pre-eclampsia defined as hypertension developing after 20 weeks gestation and the coexistence of one or more of the following new onset conditions:
  • a. Proteinuria (spot urine protein/creatinine =30 mg/mmol [0.3 mg/mg] or =300 mg/day or at least 1 g/l [‘2+’] on dipstick testing)
  • b. Other maternal organ dysfunction:
  • - renal insufficiency (creatinine =90 Umol/l)
  • - liver involvement (elevated transaminases – at least twice upper limit of normal ± right upper quadrant or epigastric abdominal pain)
  • - neurological complications (examples include eclampsia, altered mental status, blindness, stroke, or more commonly hyperreflexia when accompanied by clonus, severe headaches when accompanied by hyperreflexia, persistent visual scotomata)
  • - hematological complications (thrombocytopenia – platelet count below 150,000/dL, DIC, hemolysis))
  • c. Uteroplacental dysfunction
  • - fetal growth restriction
  • 5. Provided written informed consent.
  • 6. Willingness and ability to comply with all protocol procedures.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 15
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

Exclusion Criteria

  • 1. Impending Fetal death compromise – absent end-diastolic umbilical artery flow, pathological CTG
  • 2. Any known fetal abnormality
  • 3. Patients diagnosed with hereditary angioedema (HAE)
  • 4. Medical history of allergy to rabbits or rabbit-derived products (including rhC1INH)
  • 5. Treatment with any investigational drug during the current pregnancy
  • 6. Patient with known chronic hypertension requiring antihypertensive treatment
  • 7. Patient with abnormalities in their clotting system.
  • 8. Patient with known renal and/or hepatic abnormality
  • 9. Patient with a history of malignancy (except if determined cured or on remission for at least 5 years)
  • 10. Medical history of any organ transplants
  • 11. Uncontrolled diabetes, defined as HbA1C > 7%
  • 12. Currently treated with statins
  • 13. Any other condition or treatment that, in the opinion of the Investigator, might interfere with the evaluation of study objectives

Investigators

Similar Trials