🏛️ Verified NIH Record • Updated 2026-08-10

A Study to Assess the Effect of Surovatamig in Adult Participants With Antibody-mediated Kidney Disease (NCT07571746)

A Phase 2, Open-label Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of Surovatamig in Adults With Antibody-mediated Kidney Disease

🟢 Recruiting Phase2 💊 Investigational Drug / Biologic Sponsor: AstraZeneca

🩺 Plain-English Summary (8th-Grade Level)

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.

Who can join: Review the eligibility criteria below.

Location: Research Site — Los Angeles, California

Age range: 18 Years to 75 Years

🧪 Interventions in This Study

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (24 Sites)

  • Research Site — Los Angeles, California
  • Research Site — Los Angeles, California
  • Research Site — Iowa City, Iowa
  • Research Site — Bethesda, Maryland
  • Research Site — New York, New York
  • Research Site — Houston, Texas
  • Research Site — Houston, Texas
  • Research Site — Ieper,
  • Research Site — Bordeaux,
  • Research Site — Créteil,
  • Research Site — Lyon,
  • Research Site — Nantes,
  • Research Site — Nîmes,
  • Research Site — Düsseldorf,
  • Research Site — München,
  • Research Site — Brescia,
  • Research Site — Rozzano,
  • Research Site — Torino,
  • Research Site — Verona,
  • Research Site — Lodz,
  • Research Site — Barcelona,
  • Research Site — Madrid,
  • Research Site — London,
  • Research Site — Manchester,

📞 Contact the Study Coordinator

Phone: (877) 240-9479

Email: information.center@astrazeneca.com

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
🏛️ View Official NIH Record ↗