Systemic Lupus Erythematosus Clinical Trials
44 studies are recruiting for systemic lupus erythematosus 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.
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Studies now recruiting
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A Study to Evaluate the Efficacy and Safety of Dapirolizumab Pegol in Study Participants With Moderately to Severely Active Systemic Lupus Erythematosus
The purpose of this study is to evaluate the ability of dapirolizumab pegol (DZP) as an add-on treatment to standard of care (SOC) medication to achieve clinically relevant long term improvement of moderate to severe disease activity.
- Stage
- Phase 3
- Ages
- 16 and older
- Site
- Sl0044 50058, Avondale, Arizona
- Locations
- 245 in total
- Run by
- UCB Biopharma SRL
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Study of Systemic Lupus Erythematosus
This protocol will evaluate patients with systemic lupus erythematosus (SLE) and their relatives to learn more about how the disease develops and changes over time. It will also study genetic factors that make a person susceptible to SLE. Patients 3 years of age and older with known or suspected SL…
- Stage
- Not phased
- Ages
- 3 to 120
- Site
- National Institutes of Health Clinical Center, Bethesda, Maryland
- Run by
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
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Safety of the Herpes Zoster Subunit Vaccine in Lupus
This randomized, double-blind, placebo-controlled, non-inferiority crossover study will evaluate the Herpes Zoster Sunbit (HZ/su) vaccine in SLE patients in order to evaluate safety and immunogenicity in patients with variable baseline clinical activities, ages and immunosuppressant exposures. The …
- Stage
- Phase 4
- Ages
- 18 to 90
- Site
- NYU Langone Health, New York, New York
- Locations
- 2 in total
- Run by
- NYU Langone Health
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Study Evaluating Safety, Tolerability, PK/PD of Surovatamig in Adult RA or SLE Participants
This open-label, Phase I study will assess the safety and tolerability of surovatamig and characterise its PK and PD following subcutaneous administration to participants with RA or SLE.
- Stage
- Phase 1
- Ages
- 18 to 65
- Site
- Research Site, Fullerton, California
- Locations
- 35 in total
- Run by
- AstraZeneca
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A Study to Test Whether Different Doses of BI 3000202 Help People With Systemic Lupus Erythematosus (SLE)
This study is open to adults with systemic lupus erythematosus (SLE). The purpose of this study is to find out whether a medicine called BI 3000202 helps people with SLE. The study tests different doses of BI 3000202 and aims to find the best dose for people with this condition. Participants are pu…
- Stage
- Phase 2
- Ages
- 18 to 74
- Site
- Arthritis & Osteoporosis Medical Center, Inc - La Palma, La Palma, California
- Locations
- 139 in total
- Run by
- Boehringer Ingelheim
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A Study to Assess Adverse Events, How the Drug Moves Through the Body and Effectiveness of Intravenous Infusions and Subcutaneous Injections of ABBV-519 in Adult Participants With Systemic Lupus Erythematosus (SLE) or Rheumatoid Arthritis (RA)
Systemic lupus erythematosus (SLE) is a chronic, systemic autoimmune disease characterized by B cell hyperactivity. Rheumatoid Arthritis (RA) is a chronic inflammatory disease causing pain, stiffness, swelling and loss of joint function. The purpose of this study is to assess the pharmacokinetics, …
- Stage
- Phase 1
- Ages
- 18 to 75
- Site
- Pinnacle Research Group /ID# 278677, Anniston, Alabama
- Locations
- 15 in total
- Run by
- AbbVie
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A Study to Investigate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AZD5492 in Adult Participants With Systemic Lupus Erythematosus or Idiopathic Inflammatory Myopathies or Rheumatoid Arthritis.
The purpose of this study is to measure the safety, tolerability, PK, and PD of AZD5492 administered subcutaneously in adult participants with SLE or IIM or RA Study details include: • The study duration will be a minimum of 180 days in addition to the screening period. Additional follow-up visits …
- Stage
- Phase 1
- Ages
- 18 to 70
- Site
- Research Site, Anniston, Alabama
- Locations
- 38 in total
- Run by
- AstraZeneca
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Phase 3 Extension Study to Evaluate Long-term Safety of Ianalumab in Participants With Systemic Lupus Erythematosus (SIRIUS-SLE Extension).
The purpose of this study is to evaluate long-term safety and tolerability of ianalumab in participants with systemic lupus erythematosus who have previously completed the treatment period in one of the two SIRIUS-SLE core studies (CVAY736F12301 or CVAY736F12302).
- Stage
- Phase 3
- Ages
- 12 to 100
- Site
- Pinnacle Research Group Llc, Anniston, Alabama
- Locations
- 164 in total
- Run by
- Novartis Pharmaceuticals
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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
- 12 to 65
- Site
- University of California Irvine, Orange, California
- Locations
- 23 in total
- Run by
- Cabaletta Bio
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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
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Testing an Immunotherapy Anti-cancer Drug, Nivolumab, for Advanced Cancers in Patients With Autoimmune Disorders, AIM-NIVO
This phase Ib trial studies the side effects of nivolumab and to see how well it works alone and in combination with other treatments, such as ipilimumab, cabozantinib, platinum containing therapy, and fluoropyrimidine, in treating patients with autoimmune disorders and cancer that has spread from …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of California Davis Comprehensive Cancer Center, Sacramento, California
- Locations
- 52 in total
- Run by
- National Cancer Institute (NCI)
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A Phase 2 Master Protocol Assessing Inebilizumab and Blinatumomab in Autoimmune Diseases
The main objective is to assess the safety and tolerability of inebilizumab in adult participants with active and refractory systemic lupus erythematosus (SLE) with nephritis (Subprotocol A) and to assess the safety and tolerability of subcutaneous (SC) blinatumomab in adult participants with activ…
- Stage
- Phase 2
- Ages
- 18 to 75
- Site
- HonorHealth Research and Innovation Institute, Scottsdale, Arizona
- Locations
- 58 in total
- Run by
- Amgen
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A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase 2a Study With an Open-Label Extension Evaluating the Efficacy and Safety of VENT-03 in Adult Participants With Active Cutaneous Lupus Erythematosus With or Without Systemic Lupus Erythematosus
The goal of this clinical trial is to learn if VENT-03 works to treat patients with cutaneous lupus erythematosus (CLE) who may or may not have systemic lupus erythematosus (SLE). Another goal is to learn about the safety of VENT-03 and how it is processed by the body. The main questions it aims to…
- Stage
- Phase 2
- Ages
- 18 to 80
- Site
- Investigative Site, Beverly Hills, California
- Locations
- 34 in total
- Run by
- Ventus Therapeutics U.S., Inc.
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An Efficacy and Safety Study of Intravenous Anifrolumab to Treat Systemic Lupus Erythematosus in Pediatric Participants
A Study to Evaluate the Pharmacokinetics (PK), Pharmacodynamics (PD), Efficacy, and Safety of Anifrolumab in Children with Moderate to Severe Active Systemic Lupus Erythematosus (SLE)
- Stage
- Phase 3
- Ages
- 5 to 17
- Site
- Research Site, Phoenix, Arizona
- Locations
- 103 in total
- Run by
- AstraZeneca
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A Study to Evaluate the Treatment Outcomes of Subcutaneous Anifrolumab in Immunosuppressant-naïve and Biologic-naïve Systemic Lupus Erythematosus
The purpose of the SUNFLOWER study is to describe clinical outcomes, including DORIS remission, achieved following the initiation of anifrolumab 120 mg SC once weekly (QW) as add-on therapy to an anti-malarial, with or without GC; in patients not in LLDAS at enrolment. Patients will be naïve to any…
- Stage
- Phase 3
- Ages
- 18 to 70
- Site
- Research Site, La Palma, California
- Locations
- 107 in total
- Run by
- AstraZeneca
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The Role of Anifrolumab in Improving Markers of Vascular Risk in Patients With Systemic Lupus Erythematosus (SLE) - IFN-CVD
Background: People with systemic lupus erythematosus (SLE) are at risk of developing complications in their blood vessels. This can increase the risk of heart attacks or stroke. No medications have been effective at reducing this risk in people with lupus. Objective: To test whether a drug (anifrol…
- Stage
- Phase 2
- Ages
- 18 to 80
- Site
- National Institutes of Health Clinical Center, Bethesda, Maryland
- Run by
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
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Anifrolumab Pregnancy Study
This is a non-interventional multi-database post-authorisation study to assess pregnancy-related safety data from women with SLE exposed to Anifrolumab.
- Stage
- Not phased
- Ages
- 18 to 130
- Site
- Research Site, Cary, North Carolina
- Run by
- AstraZeneca
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Transcutaneous Vagus Nerve Stimulation in SLE
Systemic lupus erythematosus (SLE) is a chronic autoimmune inflammatory disease. Joint and muscle pain and fatigue are extremely common among patients and contribute to a reduced quality of life. Available therapies may be associated with significant side effects and many patients do not achieve an…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Feinstein Institutes for Medical Research, Manhasset, New York
- Run by
- Northwell Health
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Prospective Registry Investigating Maternal, Infant, and Lactation Outcomes in Anifrolumab Users
Prospective Registry Investigating Maternal, Infant, and Lactation Outcomes in Anifrolumab Users (PRIMULA Lac) is a Post Marketing Requirements (PMR) study designed to fulfill the FDA post-marketing requirements. The study will collect data about the presence of anifrolumab in human breast milk and…
- Stage
- Phase 4
- Ages
- 18 to 130
- Site
- Research Site, Las Vegas, Nevada
- Run by
- AstraZeneca
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HEALTH Home Urinalysis Testing
Study participants enrolled in the SAMPLE Biorepository (s14-00487) who have provided permission to be contacted for future research will be enrolled and randomized (1:1) two-arm controlled) to either 1) perform weekly home-based proteinuria testing in addition to standard of care or 2) standard of…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- NYU Langone Health, New York, New York
- Run by
- NYU Langone Health
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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
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Prospective Registry Investigating Maternal and Infant Outcomes in Anifrolumab Users
PRIMULA Preg (Prospective Registry Investigating Maternal and Infant Outcomes in Anifrolumab Users) is a prospective, observational cohort study designed to evaluate the association between anifrolumab exposure during pregnancy and subsequent adverse maternal, fetal, and infant outcomes. This study…
- Stage
- Not phased
- Ages
- Any age
- Site
- Research Site, Wilmington, North Carolina
- Run by
- AstraZeneca
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Effects of Stopping Hydroxychloroquine in Elderly Lupus Disease
Hydroxychloroquine (HCQ) is a systemic lupus erythematosus (SLE) medication that has been very effective in reducing lupus disease activity and keeping patients stable with reduced symptoms. Despite a track record of safety with regard to infection compared to traditional immunosuppressive agents, …
- Stage
- Phase 3
- Ages
- 55 and older
- Site
- University of California, Los Angeles, Los Angeles, California
- Locations
- 12 in total
- Run by
- NYU Langone Health
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Intervention to Improve Communication and Medication Adherence in Lupus
CO-LEAD is an intervention to improve patient-provider communication and medication adherence among patients with systemic lupus erythematosus (SLE). The purpose of this study is to optimize the culturally appropriate delivery and test the effect of the CO-LEAD intervention, which includes the foll…
- Stage
- Not phased
- Ages
- 18 to 90
- Site
- Duke University, Durham, North Carolina
- Run by
- Duke University
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A Study to Assess Adverse Events, How the Drug Moves Through the Body and Effectiveness of Intravenous Infusions of ABBV-319 in Adult Participants With Systemic Lupus Erythematosus (SLE), Sjogren's Disease (SjD) and Rheumatoid Arthritis (RA)
Systemic lupus erythematosus (SLE) is a chronic, systemic autoimmune disease characterized by B cell hyperactivity. Sjorgren's disease (SjD) is a chronic, multisystem autoimmune disease characterized by lacrimal and salivary gland inflammation, with resultant dryness of the eyes and mouth and occas…
- Stage
- Phase 1
- Ages
- 18 to 75
- Site
- Life Clinical Trials - Colonial Drive - Margate /ID# 276050, Margate, Florida
- Locations
- 11 in total
- Run by
- AbbVie
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.