Clinical Trials in Italy / NCT06242327
Recruiting
Observational
An Outcome Analysis of Primary Membranous Nephropathy
NCT06242327 · tracked via the Priya Life Science Italy tracker
Condition(s) studied
Membranous Nephropathy
Study summary
This is an observational study intended to track the course of the primary membranous nephropathy disease in real-world clinical practice.
The study will primarily assess the long-term outcomes of patients with primary membranous nephropathy in the context of advances in treatment options.
Eligibility
Inclusion Criteria:
* Adults (≥18 years old) on the day of signing informed consent.
* Diagnosis of primary membranous nephropathy
* Nephrotic syndrome (proteinuria \>3.5 g/24 hours)
* Written informed consent to the use of recorded data for research purposes.
Exclusion Criteria:
* Legal incapacity or limited legal capacity.
* Any contraindication to treatment with rituximab or other monoclonal antibody
Primary outcome measure(s)
- Evaluation of disease remission — Through study completion, an average of 6 months
Combined endpoint of complete (proteinuria \< 0.3 g/24-hours) or partial (proteinuria \<3 g/24-hours with \>50% change vs proteinuria at baseline that is the time of the first rituximab or other monoclonal antibody administration) remission
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| ASST HPG23 - Unità di Nefrologia | Bergamo | BG | Active Not Recruiting |
| Centro di Ricerche Cliniche per le Malattie Rare "Aldo e Cele Daccò" | Ranica | BG | Recruiting |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06242327 on ClinicalTrials.gov ↗ ← All trials in Italy