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Recruiting Observational

An Outcome Analysis of Primary Membranous Nephropathy

NCT06242327 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2024-11-29
Last updated
2026-03-23

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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
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)

FacilityCityRegionStatus
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

Other trials for the same condition

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