A Study to Learn More About the Effects and Safety of Felzartamab Infusions in Adults With Primary Membranous Nephropathy (PMN) (NCT06962800)
An Open-Label, Multicenter, Randomized Phase 3 Study Evaluating the Efficacy and Safety of Felzartamab in Participants With Primary Membranous Nephropathy (PMN) [PROMINENT]
🩺 Plain-English Summary (8th-Grade Level)
In this study, researchers will learn more about the use of felzartamab in participants with primary membranous nephropathy, also known as PMN. In people with PMN, autoantibodies build up in the glomeruli of the kidney. Antibodies are proteins that help the body fight off infection. An autoantibody is a type of antibody that mistakenly targets and attacks the body's own tissues. Glomeruli are the filters of the kidney that remove waste and extra fluid from the body. In PMN, the build-up of autoantibodies in the glomeruli causes damage to the kidneys. Kidney damage can lead to too much protein and blood leaking into the urine. High levels of protein in the urine, called proteinuria, are common in people with PMN. Symptoms of PMN can include swelling in the legs and body, tiredness, and high blood pressure. If left untreated, PMN can eventually lead to kidney failure. In this study, researchers will learn more about how a study drug called felzartamab affects people with PMN. Felzartamab is a monoclonal antibody, which means it is an antibody made in a laboratory. Felzartamab can target immune cells that produce autoantibodies, helping to lower their buildup in the kidneys. The main goal of this study is to compare how felzartamab works compared to a drug called tacrolimus. Tacrolimus is another drug given to people with PMN and kidney disease. The main question that researchers want to answer is: * How many participants achieve a complete response after 104 weeks of treatment? * A complete response means that their urine protein levels decrease to a low level and their kidney function remains stable. Researchers will also learn about: * How long it takes before the participants' disease gets worse * How long the participants' urine protein levels stay low * How many participants develop antibodies against felzartamab in the blood? * How many participants achieve a complete response after 76 weeks of treatment * How many participants have medical problems during the study * How felzartamab is processed by the body * How felzartamab affects participants' tiredness and overall physical health The study will be done as follows: * Participants will be screened to check if they can join the study. This may take up to 42 days. * Participants will be randomized to receive either felzartamab as intravenous (IV) infusions or tacrolimus, taken orally as tablets. * If participants have worsening kidney function or worsening proteinuria, or if their PMN relapses, or if they show no signs of improvement in their PMN, they will have a chance to receive rescue treatment. * If a participant stops treatment early, there will be follow-up visits every 12 weeks until they reach Week 104. * In total, participants will have up to 23 study visits. Participants who do not need rescue treatment will stay in the study for up to 104 weeks. Participants who need rescue treatment will stay in the study for up to 156 weeks.
Who can join: Review the eligibility criteria below.
Location: Apogee Clinical Research, LLC — Huntsville, Alabama
Age range: 18 Years to 80 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (112 Sites)
Showing the first 25 of 112 sites.
- Apogee Clinical Research, LLC — Huntsville, Alabama
- The Nephrology Group, Inc. - Fresno — Fresno, California
- Academic Medical Research Institute — Los Angeles, California
- UCLA Health Connie Frank Kidney Transplant Center and General Nephrology — Los Angeles, California
- UCSF Medical Center — San Francisco, California
- Stanford University — Stanford, California
- Henry Ford Hospital- A-Basement Research Pharmacy — Detroit, Michigan
- Elixia Health - Michigan Kidney Consultants, LLC - Elixia - PPDS — Pontiac, Michigan
- James J Peters Veterans Administration Medical Center - NAVREF - PPDS — The Bronx, New York
- ECU Physicians Nephrology and Hypertension — Greenville, North Carolina
- University Hospitals Cleveland Medical Center — Cleveland, Ohio
- Knoxville Kidney Center, PLLC — Knoxville, Tennessee
- Vanderbilt University Medical Center — Nashville, Tennessee
- Nephrotex Research Group — Dallas, Texas
- University of Texas Medical Branch — League City, Texas
- University of Wisconsin School of Medicine and Public Health — Madison, Wisconsin
- Organización Médica de Investigación — Buenos Aires,
- CINME S.A. - Centro de Investigaciones Metabólicas — Buenos Aires,
- Hospital Italiano de Buenos Aires — Buenos Aires,
- Centro Medico Dra. Laura Maffei- Investigacion Clinica Aplicada — Buenos Aires,
- Clínica Privada Vélez Sarsfield — Córdoba,
- Concord Hospital — Concord, New South Wales
- St George Hospital — Kogarah, New South Wales
- Liverpool Hospital — Liverpool, New South Wales
- Westmead Hospital — Westmead, New South Wales
📞 Contact the Study Coordinator
Phone: (866) 633-4636
Email: clinicaltrials@biogen.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.
More studies in Primary Membranous Nephropathy
- A Study to Examine the Efficacy and Safety of Zanubrutinib Given to Adults With Primary Membranous Nephropathy — Granada Hills, California
- A Study Evaluating the Efficacy and Safety of Obinutuzumab in Participants With Primary Membranous Nephropathy — San Francisco, California
- Evaluation of Efficacy, Safety, and Tolerability of Povetacicept in Participants With Primary Membranous Nephropathy (pMN) — Montgomery, Alabama
- Study of ALXN1920 in Adult Participants With Primary Membranous Nephropathy (PMN) — Loma Linda, California
- A Phase 2 Study of Budoprutug in Subjects With Primary Membranous Nephropathy — Denver, Colorado
Explore by condition: All Primary Membranous Nephropathy clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.