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
Conditions
Drugs
Trial Snapshot
- Phase
- Phase 1
- Status
- Active, not recruiting
- Sponsor
- Pharming Technologies B.V.
- 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
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