Lupus Nephritis Clinical Trials
19 studies are recruiting for lupus nephritis in the United States right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
Search these by distance from you
By city
Studies now recruiting
-
VIBRANT: VIB4920 for Active Lupus Nephritis
This is a multi-center double-blind placebo controlled clinical trial evaluating the efficacy of VIB4920 combined with mycophenolate mofetil (MMF) and prednisone in achieving a renal response in participants with active lupus nephritis (LN).
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- University of California San Diego School of Medicine: Division of Rheumatology, Allergy and Immunology, La Jolla, California
- Locations
- 17 in total
- Run by
- National Institute of Allergy and Infectious Diseases (NIAID)
-
The Pediatric Lupus Nephritis Mycophenolate Mofetil (PLUMM) Study
The study is a 1-year 2-part double-blinded placebo controlled 2-arm clinical trial. Treatment arms are (1) MMF dosed as per body-surface area (MMFBSA; 600mg/m2 body surface area per dose about every 12 hours) and (2) pharmacokinetically-guided precision-dosing of MMF (MMFPK; MMF dosed twice daily …
- Stage
- Phase 2
- Ages
- 8 to 20
- Site
- University of California, San Francisco, San Francisco, California
- Locations
- 19 in total
- Run by
- Children's Hospital Medical Center, Cincinnati
-
A Phase 2, Open-Label, Single-Arm Trial of FT819 in Participants With Lupus Nephritis
The primary objective of this trial is to evaluate the efficacy and safety of FT819, comprised of allogeneic T cells that express a CD19-targeted CAR, following bendamustine administration in participants with refractory moderate-to-severe lupus nephritis, as assessed by the proportion of participa…
- Stage
- Phase 2
- Ages
- 12 to 70
- Site
- Wallace Rheumatic Studies Center, Beverly Hills, California
- Locations
- 12 in total
- Run by
- Fate Therapeutics
-
Phase III Extension Study of Efficacy and Safety of Ianalumab With or Without Study Treatment Withdrawal in Participants With Lupus Nephritis (SIRIUS-LN Extension)
The purpose of this up to 6-year extension study is the evaluation of the efficacy and safety 1. after study treatment withdrawal in patients with lupus nephritis (LN) who achieved response (complete renal response [CRR] or partial renal response [PRR]) on double-blind treatment at the end of the S…
- Stage
- Phase 3
- Ages
- 18 to 100
- Site
- Circuit Clinical, Orchard Park, New York
- Locations
- 49 in total
- Run by
- Novartis Pharmaceuticals
-
A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Obinutuzumab in Adolescents With Active Class III or IV Lupus Nephritis and the Safety and PK of Obinutuzumab in Pediatric Participants
This phase II, randomized, double-blind, placebo-controlled study is designed to evaluate the safety, efficacy and pharmacokinetics (PK) of obinutuzumab in adolescent participants (AP) aged 12 to less than 18 with biopsy-confirmed proliferative lupus nephritis (LN). It will also evaluate open label…
- Stage
- Phase 2
- Ages
- 5 to 17
- Site
- Loma Linda University health, Loma Linda, California
- Locations
- 43 in total
- Run by
- Hoffmann-La Roche
-
A Safety and Efficacy Study Evaluating CTX112 in Adult Subjects With Refractory Autoimmune Disease
This is a single-arm, open-label, multicenter, ascending dose Phase 1 study evaluating the safety and preliminary efficacy of CTX112 in adult subjects with refractory autoimmune diseases, including active systemic lupus erythematosus (SLE), systemic sclerosis (SSc), or idiopathic inflammatory myopa…
- Stage
- Phase 1
- Ages
- 18 to 70
- Site
- Stanford University Medical Center, Redwood City, California
- Locations
- 16 in total
- Run by
- CRISPR Therapeutics
-
RESET-SLE: A Phase 1/2 Open-Label Study to Evaluate the Safety and Efficacy of CABA-201 in Subjects With Active Systemic Lupus Erythematosus
RESET-SLE: A Phase 1/2 Open-Label Study to Evaluate the Safety and Efficacy of CABA-201 in Subjects With Active Systemic Lupus Erythematosus
- Stage
- Phase 1
- Ages
- 18 to 65
- Site
- University of California Irvine, Orange, California
- Locations
- 23 in total
- Run by
- Cabaletta Bio
-
Obe-cel in Severe, Refractory Systemic Lupus Erythematosus (SLE) With Active Lupus Nephritis (LN)
The purpose of this trial is to evaluate the efficacy and safety of obecabtagene autoleucel (obe-cel) administered once following lymphodepletion in participants with severe, refractory systemic lupus erythematosus (SLE) and active lupus nephritis (LN).
- Stage
- Phase 2
- Ages
- 12 to 65
- Site
- Icahn School of Medicine at Mount Sinai, New York, New York
- Locations
- 15 in total
- Run by
- Autolus Limited
-
PRESERVE: LUPKYNIS in Combination With Belimumab, Obinutuzumab or Anifrolumab in Patients With Lupus Nephritis
The goal of this clinical study is to assess the efficacy and safety of LUPKYNIS® in combination with belimumab, obinutuzumab or anifrolumab at inducing rapid renal response in patients with lupus nephritis (LN).
- Stage
- Phase 4
- Ages
- 18 to 75
- Site
- Purushotham & Akther Kotha MD, Inc., La Mesa, California
- Locations
- 27 in total
- Run by
- Aurinia Pharmaceuticals Inc.
-
Study of Efficacy and Safety of LNP023 in Participants With Active Lupus Nephritis Class III-IV, +/- V
The overall purpose of this two-part study is to evaluate the efficacy, safety and tolerability of iptacopan (LNP023) in addition to standard of care treatment.
- Stage
- Phase 2
- Ages
- 18 to 100
- Site
- Ronald Reagan UCLA Medical Center, Los Angeles, California
- Locations
- 103 in total
- Run by
- Novartis Pharmaceuticals
-
Wellness & Workforce Solution for Lupus/Lupus Nephritis
The investigators will test the hypothesis that culturally congruent coaching delivered via a technology application (Health360x) will improve the persistent disparities observed among women of color with lupus or lupus nephritis by addressing underlying psychosocial barriers to behavioral change.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Morehouse School of Medicine, Atlanta, Georgia
- Run by
- Morehouse School of Medicine
-
Study to Assess Real-world Effectiveness of Belimumab for Treatment of Adults With LN
The purpose of the OBSErve-LN study is to assess the real-world use and effectiveness of belimumab in routine practice for the treatment of adults with active LN in multiple countries of interest. This study aims to provide the first long-term (up to 5 years) assessment of renal function preservati…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- GSK Investigational Site, Baltimore, Maryland
- Locations
- 7 in total
- Run by
- GlaxoSmithKline
-
US Zamto-cel Autoimmune Diseases
AID is a phase I multi-cohort study to assess the safety and tolerability of zamtocabtagene autoleucel (zamto-cel) in patients with refractory autoimmune diseases (SLE-Non renal, SLE-LN, SSc/dcSSc) after receiving standard therapy.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Froedtert Hospital and the Medical College of Wisconsin, Milwaukee, Wisconsin
- Run by
- Miltenyi Biomedicine GmbH
-
A Phase 1/2 Study of NKX019 in Subjects With Autoimmune Disease (Ntrust-1)
This is a Phase 1/2, open-label, multi-center, multi-cohort, non-randomized dose escalation and dose expansion basket study to determine the safety and tolerability of NKX019 (allogeneic CAR NK cells targeting CD19) in participants with autoimmune diseases.
- Stage
- Phase 1
- Ages
- 18 to 75
- Site
- Nkarta Investigational Site, Little Rock, Arkansas
- Locations
- 19 in total
- Run by
- Nkarta, Inc.
-
A Phase 1 Study of FT819 in B-cell Mediated Autoimmune Disease
This is a phase 1 study designed to evaluate the safety, pharmacokinetics (PK), and anti-B-cell activity of FT819 following treatment with or without auxiliary medicinal product (AMP) in participants with moderate-to-severe active systemic lupus erythematosus (SLE) with or without nephritis, antine…
- Stage
- Phase 1
- Ages
- 12 to 70
- Site
- Wallace Rheumatic Center, Beverly Hills, California
- Locations
- 21 in total
- Run by
- Fate Therapeutics
-
Lupus Landmark Study: A Prospective Registry and Biorepository
The purpose of the registry and biorepository is to provide a mechanism to store clinical data, linked biospecimens and molecular data to support the conduct of future research on Systemic Lupus Erythematosus (SLE), including Lupus Nephritis (LN).
- Stage
- Not phased
- Ages
- 18 to 110
- Site
- University of Alabama at Birmingham, Birmingham, Alabama
- Locations
- 25 in total
- Run by
- Lupus Research Alliance
-
Phase I/II Study of AD-PluReceptor Plus Tafasitamab-cxix and Lymphodepleting Chemotherapy in Patients With Autoimmune Disorders
The goal of Safety Lead-In is to confirm the safety of tafasitamab when given to patients with SSc, SLE, and LN. The goal of Phase 1 is to find the recommended dose of AD-PluReceptor-NK cells in combination with tafasitamab and lymphodepleting chemotherapy that can be given to patients with the dis…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- MD Anderson Cancer Center, Houston, Texas
- Locations
- 2 in total
- Run by
- M.D. Anderson Cancer Center
-
Safety and Efficacy of Combination Belimumab and Voclosporin in the Treatment of Proliferative Forms of Lupus Glomerulopathy: Synergy Trial
This is a Phase IV, open-label, randomized trial to determine whether the combination of Belimumab (BEL) and Voclosporin (VCS), plus background therapy with Mycophenolate Mofetil (MMF), improves the proportion of patients with proliferative lupus nephritis achieving complete renal response (CRR) co…
- Stage
- Phase 4
- Ages
- 18 to 80
- Site
- AARA Clinical Research, Glendale, Arizona
- Locations
- 7 in total
- Run by
- NephroNet, Inc.
-
Repository of Novel Analytes Leading to Autoimmune, Inflammatory and Diabetic Nephropathies (RENAL AID)
A central goal of this data repository is to collect data from a large population of subjects with a variety of renal disease states. Cohorts will include subjects with diabetes, inflammatory/autoimmune and transplant related renal conditions. Additionally, the repository will have the capacity to …
- Stage
- Not phased
- Ages
- 18 and older
- Site
- The Rogosin Institute, New York, New York
- Run by
- The Rogosin Institute
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.
Paid placement. Some studies pay us when someone asks to be connected to them. Those are labelled Sponsored wherever they appear, and they only appear when they match what you were actually looking for.