ClinicaliQ Trial Snapshot
- A Study to Assess the Effect of Surovatamig in Adult Participants With Antibody-mediated Kidney Disease — Recruiting • Phase II • NCT07571746.
- What is being tested: Surovatamig, a novel subcutaneous therapeutic agent, is being evaluated for its safety, tolerability, pharmacokinetics, and efficacy in treating primary membranous nephropathy—an antibody-mediated kidney disease causing proteinuria and progressive renal dysfunction.
- Patient eligibility overview: The trial enrolls adult participants with confirmed primary membranous nephropathy, representing a patient population at risk of progressive kidney disease and renal failure without effective disease-modifying treatments.
Use This Page For
- Quick orientation before opening the registry record.
- Checking recruitment status, phase and sponsor at a glance.
- Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying
The purpose of this study is to assess the safety, tolerability, pharmacokinetic, and efficacy of surovatamig administered by subcutaneous injection in adult participants with primary membranous nephropathy.
Eligibility Snapshot
- :
- Participant must be 18 (or the legal age of consent in the jurisdiction in which the study is taking place) to 75 years of age inclusive, at the time of signing the informed consent. 2. Diagnosis of anti-PLA2R antibody-positive pMN. 3. All participants must have received SoC therapy with angiotensin-converting enzyme inhibitors or angiotensin receptor blockers for ≥ 4 weeks, with exceptions in case of intolerance, contraindications, or low blood pressure, before the screening period. 4. Positive for anti-PLA2R. 5. Up to date with required vaccinations as per institutional guidelines (eg, influenza, pneumococcal, and severe acute respiratory syndrome coronavirus 2) prior to study entry. 6. Male and/or female assigned at birth, inclusive of all gender identities. Contraceptive use by participants or participant partners should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies. 7. Capable of giving signed informed consent
Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.