🏛️ Verified NIH Record • Updated 2026-07-31

Evaluation of Efficacy, Safety, and Tolerability of Povetacicept in Participants With Primary Membranous Nephropathy (pMN) (NCT07204275)

A Phase 2b/3 Adaptive, Randomized, Active-controlled Study Evaluating the Efficacy, Safety, and Tolerability of Povetacicept Versus Calcineurin Inhibitor in the Treatment of Primary Membranous Nephropathy

🟢 Recruiting Phase2 / Phase3 💊 Investigational Drug / Biologic Sponsor: Vertex Pharmaceuticals Incorporated

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

The purpose of this study is to evaluate the efficacy, safety, and tolerability of povetacicept in participants with primary membranous nephropathy (pMN).

Who can join: Review the eligibility criteria below.

Location: Renal Associates — Montgomery, Alabama

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 (111 Sites)

Showing the first 25 of 111 sites.

  • Renal Associates — Montgomery, Alabama
  • Southwest Kidney Institute, PLC (SKI) - Surprise — Surprise, Arizona
  • Academic Medical Research Institute (AMRI) — Los Angeles, California
  • Valiance Clinical Research - Internal Medicine — Tarzana, California
  • Western Nephrology & Metabolic Bone Disease PC — Arvada, Colorado
  • Bioresearch Partner — Miami, Florida
  • CTR Oakwater, LLC — Orlando, Florida
  • Clinical Site Partners, LLC - Orlando — Winter Park, Florida
  • DaVita Clinical Research Columbus — Columbus, Georgia
  • Georgia Nephrology — Lawrenceville, Georgia
  • CARE Institute-Boise Kidney — Boise, Idaho
  • NANI Research — Hinsdale, Illinois
  • DaVita Clinical Research Edina — Edina, Minnesota
  • St. Clair Nephrology Research — Roseville, Missouri
  • Kidney Specialists of Southern Nevada — Las Vegas, Nevada
  • NYU Medical Center — New York, New York
  • Carolina Nephrology Greenville — Greenville, South Carolina
  • Carolina Nephrology, PA — Spartanburg, South Carolina
  • El Paso Kidney Specialists — El Paso, Texas
  • Provecta Research Network — Houston, Texas
  • DaVita Clinical Research Houston — Houston, Texas
  • Davita Clinical Research San Antonio — San Antonio, Texas
  • Utah Kidney Research — Salt Lake City, Utah
  • Milwaukee Neprologists, SC — Wauwatosa, Wisconsin
  • Monash Medical Centre — Clayton,

📞 Contact the Study Coordinator

Phone: 001-617-341-6777

Email: medicalinfo@vrtx.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 ↗