Actively Recruiting
Eculizumab in Hypertensive Emergency-associated Hemolytic Uremic Syndrome
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2024-01-05
66
Participants Needed
1
Research Sites
208 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Hemolytic and uremic syndrome (HUS) is a clinic-biological syndrome related to thrombotic microangiopathy affecting predominantly the kidney. Atypical HUS (aHUS) has been historically defined as HUS occurring in the absence of infectious event. The role of complement dysregulation in aHUS pathophysiology has been largely demonstrated, since C genetic rare variants are present in 60-70% aHUS patients. In line with the frequency of C dysregulation in aHUS, Eculizumab, an anti-C5 monoclonal antibody, has dramatically improved aHUS patients prognosis. Numerous conditions have been associated with aHUS, including hypertensive emergency (HE), a syndrome of acute blood pressure flare associated with end-organ damage. In cases of HE-aHUS, whether primary aHUS is complicated by secondary HE, or primary HE leads to secondary aHUS is still debated. The investigators recently demonstrated that C genetic variants frequency was similar in patients with HE-aHUS and patients with aHUS without HE, suggesting a major role for C dysregulation in HE-aHUS. Consequently, the investigators propose to evaluate, in HE-aHUS patients, the benefit of a strategy with early Eculizumab therapy (used within its marketing authorization and its conditions of refunding by the health insurance in usual care), compared to standard of care including tight blood pressure control. The hypothesis suggests that C dysregulation may impact renal prognosis of HE-aHUS patients. The investigator's aim to demonstrate that early Eculizumab therapy improves prognosis of HE-aHUS patients. Method The HYPERSHU study is a randomized, controlled, open-labelled study including HE-aHUS patients with severe AKI and no evidence of other conditions associated with HUS (infections, autoimmunity, drugs, pregnancy). The investigators plan to include 62 patients. Patients will be randomized in 2 arms: * Early Eculizumab therapy (for 3 months) added to standard of care (tight blood pressure control). * Standard of care alone with tight blood pressure control. Renal function after 6 months is the primary evaluation criterium. HE is a frequently associated with aHUS, and strongly impacts patient renal prognosis. Efficient therapeutic strategies are still lacking for this condition. The HYPERSHU study will allow to evaluate the benefit of early Eculizumab therapy in patients with HE-aHUS and severe renal dysfunction.
CONDITIONS
Official Title
Eculizumab in Hypertensive Emergency-associated Hemolytic Uremic Syndrome
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years of age or older
- Hospitalized within the last 10 days for hypertensive emergency-associated hemolytic uremic syndrome
- Presumed acute kidney failure requiring renal replacement therapy or with serum creatinine ≥ 354�B5M
- Signs of mechanical hemolysis including anemia, low platelet count, and low haptoglobin or high LDH or schistocytes presence
- Severe high blood pressure with systolic > 180 mmHg or diastolic > 110 mmHg
- Evidence of target organ damage such as neurological symptoms, heart failure, lung edema, chest pain, or vision problems
- Using effective contraception during the study and for at least 5 months after last Eculizumab dose
- Affiliated to a social security plan
- Signed written informed consent
You will not qualify if you...
- Small or shrunken kidneys less than 8 cm on recent imaging
- Strong suspicion of complement-mediated aHUS or family history of aHUS
- Strong suspicion of typical HUS caused by Shiga toxin-producing infection or thrombotic thrombocytopenic purpura
- Strong suspicion of secondary HUS from autoimmune diseases or C3 glomerulopathy
- Recent stroke suspected
- ADAMTS 13 activity less than 10%, HIV or HCV infection, or positive for specific autoimmune markers
- Active infection
- Unresolved Neisseria meningitidis infection
- Refusal of vaccination or antibiotic prevention for Neisseria meningitidis
- Contraindications to Eculizumab or renin angiotensin system blockers
- History of solid organ or blood stem cell transplant
- Active cancer within the past year or recent exposure to drugs associated with aHUS
- Severe cognitive or psychiatric disorders preventing informed consent
- Positive SARS-CoV-2 PCR test
- Pregnancy, breastfeeding, or ineffective contraception
- Legal restrictions such as incarceration or legal protection
- Participation in another interventional clinical trial or within exclusion period from previous trial
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Tenon Hospital
Paris, France, 75020
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here