An Open Label Phase 1b Study of Felzartamab in Lupus Nephritis

Status: Recruiting
Location: See all (29) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

In this study, researchers will learn more about the use of felzartamab in people with active lupus nephritis, also known as LN. In people with LN, antibodies build up in the glomeruli of the kidneys. Antibodies are proteins in the blood used by the immune system to fight infection. Glomeruli are small filters that remove waste and extra fluid from the blood. This buildup leads to inflammation and 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 LN. Symptoms of LN can include fever, swelling in the legs and body, and high blood pressure. If left untreated, LN can eventually lead to kidney failure. In this study, researchers will learn more about how a study drug called felzartamab affects people with LN. Felzartamab is a monoclonal antibody, which means it is an antibody made in a laboratory. Felzartamab can target immune cells that produce antibodies, helping to lower their buildup in the kidneys. The main goal of this study is to learn more about the safety of felzartamab and how it works in the body of people with LN who are taking standard of care. This will help researchers decide if they should do more studies with felzartamab in people with LN. Standard of care is the usual treatment or care given to patients for a disease, as prescribed by their doctor. The main question researchers want to answer in this study are: • How many participants had adverse events during the study? An adverse event is a health problem that may or may not be caused by the study drug. It can happen during a clinical study or within a certain amount of time after the study has ended. Researchers will also learn more about: * How much felzartamab affects proteinuria and the level of creatinine in the urine. Creatinine is a protein that is released into the blood from normal muscle wear and tear. Its levels can help doctors understand how well your kidneys are working. * How many participants have a complete response. A complete response means that their urine protein levels decrease to a low level, and their kidney function stays stable. * How many participants have a 50% decrease in the level of protein and creatinine in their urine. * How much felzartamab affects the participants' lupus-related blood tests. * How the body processes felzartamab. * How many participants develop antibodies against felzartamab in the blood. This study will be done as follows: * Participants will be screened to check if they can join the study. The screening period will be up to 42 days. * Throughout the study, all participants will continue taking their standard of care, as prescribed by their doctor. * There are 2 parts in this study. In both parts, participants will receive felzartamab through an intravenous infusion, also known as an IV. This means it is being given into a vein. * In Part 1, participants will have up to 14 visits to their study research center. In Part 2, participants may have up to 15 visits. * Each participant will be in the study for about 2 years.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

∙ Part 1

• Diagnosis of Systemic Lupus Erythematosus (SLE) according to the 2019 European League Against Rheumatism (EULAR)/ American College of Rheumatology (ACR) criteria

• Diagnosis of International Society of Nephrology/ Renal Pathology Society (ISN/RPS) 2003 Class III or IV LN as evidenced by renal biopsy performed within 1 year prior to or during screening, either with or without the presence of Class V LN

• Proteinuria (urine protein to creatinine ratio) \> 1.0 gram per gram (g/g), based on 24-hour urine collection during screening

• eGFR ≥ 45 milliliter/minute/1.73 square meters (mL/min/1.73 m\^2) (as calculated by the Chronic Kidney Disease Epidemiology Collaboration formula)

‣ If eGFR is ≥35 to \<45 mL/min/1.73m\^2, renal biopsy must be within 6 months of screening and must not have \>50% of glomeruli with sclerosis. If the renal biopsy was performed more than 6 months prior to screening, a repeat biopsy must be done during screening after all the other eligibility criteria are met

⁃ If eGFR is ≥45 mL/min/1.73 m\^2, renal biopsy must be within 1 year prior to screening. If the renal biopsy was performed more than 1 year prior to screening, a repeat biopsy must be done during screening after all the other eligibility criteria are met

• History of inadequate response, for lack of efficacy or intolerance, to at least a three-month course of one standard of care treatment for lupus nephritis, as determined by the treating physician

∙ Part 2

• Participants must complete Part 1 of the study to be eligible to participate in Part 2.

Locations
United States
Arizona
Centricity Research - Phoenix
WITHDRAWN
Mesa
California
University of California, San Diego (UCSD)
RECRUITING
La Jolla
University of California, San Francisco (UCSF)
RECRUITING
San Francisco
Stanford University Medical Center
RECRUITING
Stanford
Georgia
ClinCept, LLC/River City Vascular Specialists LLC
COMPLETED
Columbus
Georgia Nephrology - Lawrenceville
RECRUITING
Lawrenceville
Michigan
University of Michigan
RECRUITING
Ann Arbor
New York
Joseph S. and Diane H. Steinberg Ambulatory Care Center
RECRUITING
Brooklyn
SUNY Downstate Medical Center
COMPLETED
Brooklyn
Ohio
University Hospitals Cleveland Medical Center
RECRUITING
Cleveland
The Ohio State University (OSU)
RECRUITING
Columbus
Texas
Precision Comprehensive Clinical Research Solutions - Grapevine
RECRUITING
Grapevine
Prolato Clinical Research Center
COMPLETED
Houston
Accurate Clinical Research - Katy
RECRUITING
Katy
R & H Clinical Research
RECRUITING
Katy
Other Locations
Argentina
CEMIC
RECRUITING
Caba
Hospital Britanico de Buenos Aires
RECRUITING
Caba
Clinica Priv Velez Sarsfield
RECRUITING
Córdoba
Australia
Monash Health
RECRUITING
Melbourne
Western Health
RECRUITING
Saint Albans
Westmead Hospital
RECRUITING
Westmead
Princess Alexandra Hospital
RECRUITING
Woolloongabba
Canada
Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM)
RECRUITING
Montreal
University Health Network - Toronto General Division
RECRUITING
Toronto
St. Paul's Hospital
RECRUITING
Vancouver
Mexico
Servicios Avanzados de Investigación Médica/ Mediadvance Clinical S.C.
NOT_YET_RECRUITING
Chihuahua City
Centro Integral en Reumatología S.A. de C.V.
NOT_YET_RECRUITING
Guadalajara
Medical Care and Research S.A de C.V.
NOT_YET_RECRUITING
Mérida
Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
NOT_YET_RECRUITING
Mexico City
Contact Information
Primary
US Biogen Clinical Trial Center
clinicaltrials@biogen.com
1-866-633-4636
Backup
Global Biogen Clinical Trial Center
clinicaltrials@biogen.com
Time Frame
Start Date: 2023-11-01
Estimated Completion Date: 2026-06-01
Participants
Target number of participants: 20
Treatments
Experimental: Felzartamab
Participants will receive two courses of multiple intravenous (IV) doses of felzartamab, separated by a 28-week off-treatment period.~These courses are given in Part 1 and Part 2 of the trial.
Sponsors
Leads: HI-Bio, A Biogen Company

This content was sourced from clinicaltrials.gov

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