Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).
This page lists clinical trials related to Rheumatoid Arthritis from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 30
- Active, not recruiting: 7
- Completed: 6
- Other: 7
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT02327884 — Characterization of Diseases With Salivary Gland Involvement
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Dental and Craniofacial Research (NIDCR) |
| Enrollment | 1150 |
| Study Type | OBSERVATIONAL |
| Conditions | Healthy Volunteer; Sjogren’s Syndrome; Salivary Gland Disease |
Background:
- Salivary glands in and around the mouth and throat make saliva. Salivary gland disorders can affect a person s quality of life. Studying people who have a disease that affects their salivary gland(s) may teach researchers about the disorders and their genetics.
Objectives:
- To study salivary gland diseases and disorders. To collect data and samples from people with salivary …
NCT03510442 — Natural History, Genetics, and Pathophysiology of Systemic Juvenile Idiopathic Arthritis, Adult-Onset Still’s Disease, and Related Conditions
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) |
| Enrollment | 2000 |
| Study Type | OBSERVATIONAL |
| Conditions | Still’s Disease, Adult-Onset; Systemic Inflammation; Arthritis; Autoinflammatory Syndrome |
Background:
Inflammatory conditions can cause symptoms like fevers, arthritis, and rash. Systemic juvenile idiopathic arthritis (sJIA) is one of these conditions. So is adult-onset Still s disease (AOSD). Their causes are unknown. Researchers want to learn more about these conditions. This includes genetic changes and environmental factors.
Objective:
To study sJIA and AOSD in children and a…
NCT04931160 — B-dependant Rare AutoImmune diseaSES - Cohort of Patients With Suspected Diagnosis of Primitive Sjögren Syndrome
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University Hospital, Brest |
| Enrollment | 1000 |
| Study Type | INTERVENTIONAL |
| Conditions | Sjogren’s Syndrome |
| Interventions |
The objectif is to study the diagnosis performance of the different classification criteria in reference to the gold standard consisting of the diagnosis made by expert doctors after standardized assessment, of pSS (primary Sjogren syndrome)
NCT06551389 — Follow-up of the Systemic Lupus Erythematosus Cohort as Part of the Multidisciplinary Consultation at Brest CHRU
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University Hospital, Brest |
| Enrollment | 300 |
| Study Type | OBSERVATIONAL |
| Conditions | Systemic Lupus Erythematosus |
Systemic lupus erythematosus is a complex systemicautoimmune disease that can affect most organs of the human body.
Although they are many recommendations on the diagnosis and managment of SLE, diagnosis and therapeutic managment is still challenging.
A pluridisciplinary consultation grouping rheumatologist, nephrologist, dermatologist, gynecologist, internist and immunologists has been set u…
NCT06246123 — A Study of Jyseleca Tablet (Filgotinib Maleate) in Korean Participants
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Eisai Korea Inc. |
| Enrollment | 2040 |
| Study Type | OBSERVATIONAL |
| Conditions | Arthritis, Rheumatoid; Colitis, Ulcerative |
| Interventions |
The purpose of this study is to collect and evaluate the following information in relation to the safety and the efficacy of Jyseleca tablet (Filgotinib Maleate) 100 milligram (mg) and 200 mg in this post marketing setting: (1) Serious adverse events and adverse drug reactions (2) Unexpected adverse events and adverse drug reactions not reflected in precautions for use (3) Known adverse drug re…
NCT06201416 — Study of Single Doses of SBT777101 in Subjects With Rheumatoid Arthritis
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Sonoma Biotherapeutics, Inc. |
| Enrollment | 48 |
| Study Type | INTERVENTIONAL |
| Conditions | Rheumatoid Arthritis |
| Interventions |
This study will test the safety and effects of SBT777101 when given as a single dose to subjects with rheumatoid arthritis. It is the first study of this treatment being done in humans. Increasing dose levels will be given after the safety at lower dose levels is shown. Following completion of the initial single ascending dose cohorts, the study may evaluate alternative administration regimens …
NCT07674134 — Comparison of Oral Administration of a JAK Inhibitor in Rheumatoid Arthritis
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Centre Hospitalier Princesse Grace |
| Enrollment | 90 |
| Study Type | OBSERVATIONAL |
| Conditions | Rheumatoid Arthritis (RA) |
The aim of this study is to offer patients two treatment options: morning or evening administration of a JAK inhibitor prescribed within the framework of its marketing authorization, according to the EULAR response.
The objective is to determine whether evening administration in our patients with rheumatoid arthritis provides greater efficacy than morning administration in our patients taking …
NCT06916806 — 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.
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | AstraZeneca |
| Enrollment | 72 |
| Study Type | INTERVENTIONAL |
| Conditions | Systemic Lupus Erythematosus; Idiopathic Inflammatory Myopathies; Rheumatoid Arthritis |
| Interventions |
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 may be required up to 12 months from study start.
- Depending on the study part they are assig…
NCT07678034 — Post-Market Clinical Follow-Up (PMCF) Study Evaluating the Safety and Efficacy of Tıpmed™ Shoulder Prosthesis System
| Status | Recruiting |
| Phase | N/A |
| Sponsor | TIPMED Medical Device Manufacturing Ltd. Co. |
| Enrollment | 54 |
| Study Type | OBSERVATIONAL |
| Conditions | Glenohumeral Osteoarthritis; Proximal Humerus Fracture; Rotator Cuff Arthropathy; Rheumatoid Arthritis; Avascular Necrosis |
| Interventions | ; |
This study is designed as a prospective, multicenter, observational post-market clinical follow-up (PMCF) study to evaluate the safety and effectiveness of the Tipmed™ Shoulder Prosthesis System at 12 months postoperatively. The study population includes adult patients who undergo reverse shoulder arthroplasty (RSA) or shoulder hemiarthroplasty (HA) using the Tipmed™ implant systems due to vari…
NCT06972446 — A Study to Evaluate Different Targeted Therapies for Patients With Rheumatoid Arthritis
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | AbbVie |
| Enrollment | 180 |
| Study Type | INTERVENTIONAL |
| Conditions | Rheumatoid Arthritis |
| Interventions | ; ; |
Rheumatoid Arthritis (RA) is a chronic inflammatory disease causing pain, stiffness, swelling and loss of joint function. This study will evaluate the efficacy and safety of targeted therapies through a series of substudies for the treatment of moderately to severely active Rheumatoid Arthritis (RA).
This study currently includes 3 substudies evaluating different treatments in participants wit…
NCT07678112 — Medical Device for Sustained Remission in Rheumatoid Arthritis Treated With Biological Therapy
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Francisco J. Blanco |
| Enrollment | 184 |
| Study Type | INTERVENTIONAL |
| Conditions | Rheumatoid Arthritis (RA) |
| Interventions |
This study aims to evaluate a new tool designed to help doctors decide whether it is safe to reduce medication in patients with rheumatoid arthritis (RA) who are in remission.
Rheumatoid arthritis is a chronic inflammatory disease that affects the joints, causing pain, stiffness, and reduced mobility. Many patients receive long-term treatment with biological drugs to control the disease. When …
NCT06631638 — EMPHASYS Cup Positioning in THA With Non-Invasive Navigation (Velys Hip Navigation (VHN))
| Status | Recruiting |
| Phase | N/A |
| Sponsor | DePuy Orthopaedics |
| Enrollment | 118 |
| Study Type | INTERVENTIONAL |
| Conditions | Osteoarthritis; Traumatic Arthritis; Rheumatoid Arthritis; Congential Hip Dysplasia; Avascular Necrosis of the Femoral Head |
| Interventions |
The purpose of this research is to gather clinical and radiographic (X-ray) information about EMPHASYS™ acetabular shell (also called a hip ‘cup’) placement in total hip replacement surgery using a non-invasive surgical navigation system called VELYS™ hip navigation system with CUPTIMIZE™ Advanced Hip-Spine Analysis software.
Data collected in this study will be compared with data collected fr…
NCT07201558 — Study Evaluating Safety, Tolerability, PK/PD of Surovatamig in Adult RA or SLE Participants
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | AstraZeneca |
| Enrollment | 48 |
| Study Type | INTERVENTIONAL |
| Conditions | Rheumatoid Arthritis; Systemic Lupus Erythematosus |
| Interventions |
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.
NCT07258849 — A Study of LY4213663 in Healthy Participants and Participants With Rheumatoid Arthritis
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 141 |
| Study Type | INTERVENTIONAL |
| Conditions | Rheumatoid Arthritis (RA) |
| Interventions | ; ; |
The purpose of this study is to evaluate how well LY4213663 is tolerated and what side effects may occur in healthy participants and participants with rheumatoid arthritis (RA). The study drug will be administered either subcutaneously (SC) (under the skin) or intravenously (IV) (into a vein in the arm).
Blood tests will be performed to investigate how the body processes the study drug and how…
NCT07137598 — A Study to Assess the Efficacy and Safety of RO7790121 in Participants With Moderate to Severe Rheumatoid Arthritis Who Have Not Responded to or Who Cannot Tolerate Tumor Necrosis Factor (TNF) and/or Janus Kinase (JAK Inhibitors)
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Hoffmann-La Roche |
| Enrollment | 160 |
| Study Type | INTERVENTIONAL |
| Conditions | Rheumatoid Arthritis |
| Interventions | ; |
This study will assess the efficacy and safety of Afimkibart (also known as RO7790121) compared with placebo in participants with moderate to severe rheumatoid arthritis (RA) who have an inadequate response or intolerance to TNF and/or JAK inhibitors.
NCT07276581 — A Study to Investigate Efficacy and Safety of AZD1163 in Participants With Rheumatoid Arthritis
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | AstraZeneca |
| Enrollment | 320 |
| Study Type | INTERVENTIONAL |
| Conditions | Rheumatoid Arthritis |
| Interventions | ; |
Phase II study in participants with moderately-to-severely active rheumatoid Arthritis (RA) to evaluate efficacy and safety of AZD1163.
NCT07281456 — Safety of Tofacitinib, an Oral Janus Kinase Inhibitor, in Primary Sjogren Disease
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | National Institute of Dental and Craniofacial Research (NIDCR) |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Sjogren’s Syndrome |
| Interventions |
Background:
Sjogren disease is an autoimmune disease - that is, a disease that causes the body’s immune system to attack its own organs and tissues. Sjogren disease can affect the kidneys, lungs, or other organs. It can also cause dry mouth and eyes, fever, joint pain, rashes, and other symptoms. Researchers want to know if a drug approved to treat rheumatoid arthritis and other autoimmune dis…
NCT07295847 — A Study of AZD0120 in Autoimmune Diseases
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | AstraZeneca |
| Enrollment | 27 |
| Study Type | INTERVENTIONAL |
| Conditions | Systemic Sclerosis; Idiopathic Inflammatory Myopathies; Rheumatoid Arthritis |
| Interventions |
This trial is a Phase 1b, open-label, multi-center, clinical study of AZD0120, a BCMA/CD19 dual targeting CAR+ T-cell therapy, to evaluate the safety and tolerability in adult participants with systemic sclerosis (SSc), idiopathic inflammatory myopathies (IIM), or difficult-to-treat rheumatoid arthritis (D2T RA).
NCT07276958 — A Study of LY4298445 in Healthy Participants and Participants With Systemic Lupus Erythematosus (SLE) or Rheumatoid Arthritis (RA)
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 63 |
| Study Type | INTERVENTIONAL |
| Conditions | Healthy; Systemic Lupus Erythematosus; Rheumatoid Arthritis |
| Interventions | ; |
The purpose of this study is to investigate the safety and tolerability of LY4298445 in healthy participants and in participants with systemic lupus erythematosus (SLE) or rheumatoid arthritis (RA). Participation in the study will last up to approximately 52 weeks.
NCT07371468 — A Study of GSK5926371 in Participants With B-cell Driven Autoimmune Rheumatic Diseases (ARD)
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | GlaxoSmithKline |
| Enrollment | 44 |
| Study Type | INTERVENTIONAL |
| Conditions | Systemic Lupus Erythematosus |
| Interventions |
This is a 2-part study of GSK5926371 in participants with autoimmune rheumatic diseases (ARD). In part 1, participants will receive different doses of GSK5926371 to find a suitable priming dose. In part 2, participants will receive GSK5926371 at doses based on data from part 1. The study is aimed at testing if GSK5926371 is safe, well-tolerated, how the body processes the study drug, how it wor…
NCT07363590 — A Clinical Study of MK-1045 in People With Lupus or Rheumatoid Arthritis (MK-1045-004)
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Merck Sharp & Dohme LLC |
| Enrollment | 21 |
| Study Type | INTERVENTIONAL |
| Conditions | Systemic Lupus Erythematosus; Rheumatoid Arthritis |
| Interventions |
This study looks at a study medicine called MK-1045 in people with lupus and rheumatoid arthritis (RA). The main goal of the study is to learn about the safety of MK-1045 and if people tolerate it when they receive it at different dose levels (amounts).
NCT07416656 — Validation of Hemoglobin A1c in Patients With Inflammatory Arthritis Treated With Sulfasalazine
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Klavs Würgler Hansen |
| Enrollment | 75 |
| Study Type | OBSERVATIONAL |
| Conditions | Inflammatory Arthritis; Diabetes (DM); Rheumatoid Arthritis (RA); Type 1 Diabetes Mellitus; Type 2 Diabetes (T2DM) |
The purpose of this study is to examine whether the blood test Hemoglobin A1c (HbA1c) gives an accurate picture of blood glucose levels in patients with inflammatory arthritis who are treated with sulfasalazine. HbA1c is widely used to diagnose and monitor diabetes, but sulfasalazine can shorten red blood cell lifespan and thereby lower HbA1c values independently of actual glucose levels.
This…
NCT07293871 — Ultrasound Neuroimmune Modulation in Adults With Rheumatoid Arthritis
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Surf Therapeutics |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Rheumatoid Arthritis |
| Interventions | ; |
This two-stage, multicenter clinical trial is designed to evaluate the feasibility, safety, and preliminary efficacy of splenic ultrasound stimulation to activate immune-neuromodulation (SUSTAIN) in patients with rheumatoid arthritis (RA) and at least moderate disease activity. The findings from this trial will directly inform the design and power calculations for a future pivotal trial by iden…
NCT07526350 — MTS109 in Patients With Refractory Autoimmune Diseases
| Status | Recruiting |
| Phase | Early Phase 1 |
| Sponsor | Shanghai Changzheng Hospital |
| Enrollment | 15 |
| Study Type | INTERVENTIONAL |
| Conditions | Systemic Lupus Erythematosus; Idiopathic Inflammatory Myopathies; Systemic Sclerosis (SSc); ANCA-Associated Vasculitis (AAV); Sjogren’s Syndrome (SS) |
| Interventions |
This is the first-in-human trial of MTS109 (mRNA-LNP). The goal of this clinical trial is to evaluate the safety, tolerability of intravenous injection of MTS109 in moderate to severe autoimmune diseases.
NCT07473154 — Controlling Hyperactive Immunity With Long-lived Lymphocytes
| Status | Recruiting |
| Phase | Phase 1 / Phase 2 |
| Sponsor | Quell Therapeutics Limited |
| Enrollment | 16 |
| Study Type | INTERVENTIONAL |
| Conditions | Diffuse Cutaneous Systemic Sclerosis; Rheumatoid Arthritis (RA); Systemic Sclerosis (SSc); Autoimmune Rheumatologic Disease |
| Interventions |
This study is a Phase 1/2, open-label clinical trial to test an experimental treatment called QEL-005 in adults with two autoimmune conditions: diffuse cutaneous systemic sclerosis (dcSSc) and difficult-to-treat rheumatoid arthritis (D2TRA). The main goals are to find out whether QEL-005 is safe, how well people tolerate it, and whether it may help reduce disease activity or improve symptoms.
…
NCT07607964 — 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)
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | AbbVie |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Systemic Lupus Erythematosus; Rheumatoid Arthritis |
| Interventions | ; |
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, pharmacodynamics and safety of ABBV-519 in adult participants with SLE or RA.
This is a single a…
NCT07660029 — BloodTrackR Usability and Concordance Study (BUCS): Evaluating a Smart Home-Based Blood Collection Platform for Remote Monitoring in Rheumatoid Arthritis
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Ulster |
| Enrollment | 20 |
| Study Type | OBSERVATIONAL |
| Conditions | Rheumatoid Arthritis (RA); Remote Patient Monitoring |
| Interventions |
The BloodTrackR Usability and Concordance Study (BUCS) is evaluating a novel home-based blood collection device and companion mobile application for people with rheumatoid arthritis. Participants will use the BloodTrackR device to collect a finger-prick blood sample at home and complete symptom assessments through the app.
The study will assess how easy the device and app are to use, whether p…
NCT06312943 — “Translating Articular Biomarkers Into Diagnoses”
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Assistance Publique - Hôpitaux de Paris |
| Enrollment | 50 |
| Study Type | OBSERVATIONAL |
| Conditions | Inflammatory and Non-inflammatory Bone and Joint Diseases |
| Interventions |
Early diagnosis is a key factor in the prevention and management of rheumatic diseases. Rheumatic diseases are classically diagnosed based on criteria combining clinical, biological and radiological features. However, in up to 20% of the cases, diagnoses remain unstated and underlying rheumatic diseases unclassified, which might lead to delayed specific treatment and unfavourable clinical outco…
NCT07620392 — An Extension Study to Assess Long-Term Safety and Efficacy of Afimkibart in Participants With Rheumatoid Arthritis
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Hoffmann-La Roche |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Rheumatoid Arthritis |
| Interventions |
The study will evaluate the long-term safety and efficacy of Afimkibart (also known as RO7790121) in participants with moderate to severe Rheumatoid Arthritis (RA) who have an inadequate response or intolerance to tumor necrosis factor (TNF) and/or Janus kinase (JAK) inhibitors, and who were previously treated with Afimkibart.
NCT07515638 — Immun4Cure Cohort of Autoimmune Diseases
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University Hospital, Montpellier |
| Enrollment | 500 |
| Study Type | OBSERVATIONAL |
| Conditions | Rheumatoid Arthritis; Systemic Lupus Erythematosus; Systemic Sclerosis; Healthy Adult Volunteers |
| Interventions | ; ; |
This prospective cohort study aims to constitute a 500-participant database and biobank including 450 adults with systemic autoimmune diseases (rheumatoid arthritis, systemic lupus erythematosus, systemic sclerosis) and 50 healthy controls.
Active, Not Recruiting
NCT05197036 — A Global Clinical Study Investigating the Safety and Effectiveness of Smith and Nephew’s Porous Knee System in Patients Who Need a Total Knee Replacement Due to Degenerative Arthritis, Post-traumatic Arthritis or Inflammatory Arthritis
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Smith & Nephew, Inc. |
| Enrollment | 299 |
| Study Type | OBSERVATIONAL |
| Conditions | Osteoarthritis; Post-traumatic Arthritis; Rheumatoid Arthritis |
| Interventions |
A clinical trial investigating the safety and effectiveness of Smith and Nephew’s FDA-approved Porous Total Knee System, which is used to replace worn away and diseased knee joints. The aim of this study is to show that most patients who receive the Porous Total Knee System have reduced pain, greater mobility and a long-lasting implant post-surgery.
NCT05772325 — The Effect of Brief Versus Individually Tailored Dietary Advice on Change in Lipids, Blood Pressure, and Diet in Patients With Inflammatory Joint Disease
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Diakonhjemmet Hospital |
| Enrollment | 70 |
| Study Type | INTERVENTIONAL |
| Conditions | Rheumatoid Arthritis; Psoriatic Arthritis; Spondyloarthritis |
| Interventions | ; |
A randomized controlled study comparing brief dietary intervention with a personal, tailored dietary advice (60 min) on change in LDL-c and change in diet.
NCT05985915 — A Randomized, Double-blind 2-arm, Followed by an Open-label 1-arm, NEPTUNUS Extension Study to Assess the Long-term Safety and Efficacy of Ianalumab in Patients With Sjogrens Syndrome.
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 612 |
| Study Type | INTERVENTIONAL |
| Conditions | Sjogrens Syndrome |
| Interventions | ; |
The purpose of this study is to measure the long-term safety and tolerability of ianalumab in participants with Sjögren’s syndrome who have previously completed treatment from one of two NEPTUNUS 1 year core studies (CVAY736A2301 [NCT05350072] or CVAY736A2302 [NCT05349214]).
NCT06329401 — A Study Evaluating the Safety and Efficacy of Inhaled AP01 in Participants With Progressive Pulmonary Fibrosis
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Avalyn Pharma Inc. |
| Enrollment | 375 |
| Study Type | INTERVENTIONAL |
| Conditions | Pulmonary Fibrosis; Progressive Pulmonary Fibrosis; Pulmonary Fibrosis Secondary to Systemic Sclerosis; Pulmonary Fibrosis, Interstitial Lung Disease; Interstitial Lung Disease |
| Interventions | ; |
A randomized, double-blind, placebo-controlled clinical study to evaluate the safety and efficacy of 2 doses of inhaled pirfenidone (AP01) versus placebo on top of standard of care in participants with PPF over 52 weeks.
NCT06440629 — Effect of Proactive Therapeutic Drug Monitoring on Maintenance of Sustained Disease Control in Adults With Rheumatoid Arthritis on a Subcutaneous TNF Inhibitor: The Rheumatoid Arthritis Therapeutic DRUg Monitoring Trial (RA-DRUM)
| Status | Active, not recruiting |
| Phase | Phase 4 |
| Sponsor | Diakonhjemmet Hospital |
| Enrollment | 387 |
| Study Type | INTERVENTIONAL |
| Conditions | Rheumatoid Arthritis |
| Interventions |
The goal of this clinical trial is to compare therapeutic drug monitoring (TDM) versus Standard of care in patients with rheumatoid arthritis treated with a subcutaneous tumor necrosis factor inhibitor (adalimumab).
The main question it aims to answer is:
Is TDM superior to standard of care in order to maintain sustained disease control without flares?
Participants will be followed with bloo…
NCT06741969 — Nipocalimab in Moderate to Severe Sjogren’s Disease
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Janssen Research & Development, LLC |
| Enrollment | 655 |
| Study Type | INTERVENTIONAL |
| Conditions | Sjogrens Syndrome |
| Interventions | ; ; |
The purpose of this study is to evaluate the clinical efficacy and safety of nipocalimab in participants with moderate to severe Sjogren’s disease (SjD).
NCT07029555 — An Ascending Dose Study of PIT565 in Participants With Rheumatoid Arthritis
| Status | Active, not recruiting |
| Phase | Phase 1 |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 57 |
| Study Type | INTERVENTIONAL |
| Conditions | Rheumatoid Arthritis |
| Interventions |
The purpose of the study is to determine the safety, tolerability, and pharmacokinetics of PIT565, in participants with rheumatoid arthritis (RA).
Not Yet Recruiting
NCT07680101 — Intra-Articular Adelmidrol 2%/Hyaluronic Acid 1% With or Without m/umPEA, in Knee Pain Due to Joint Degeneration.
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Universita di Verona |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | Degenerative Joint Disease of Knee; Rheumatoid Arthritis |
| Interventions | ; |
Degenerative knee joint diseases are characterized by chronic pain, inflammation, and functional impairment. In these conditions, mast cell density in the synovial membrane is increased, resulting in an excessive release of biological mediators involved in key mechanisms of neuroinflammation and in hyaluronic acid depolymerisation. Adelmidrol acts as a preventive antioxidant due to its radical …
NCT07666594 — Mobile App-Based Yoga and Meditation in Rheumatoid Arthritis
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Tugba Civi Karaaslan |
| Enrollment | 102 |
| Study Type | INTERVENTIONAL |
| Conditions | Rheumatoid Arthritis (RA); Anxiety; Depression Anxiety Disorder; Mobile Health Technology (mHealth) |
| Interventions |
The goal of this single-blind, randomized controlled trial is to evaluate the clinical effectiveness and short-term economic impact of a mobile application-based, personalized yoga and meditation program in adult patients with Rheumatoid Arthritis (RA).
The main questions it aims to answer are:
Does an 8-week digital yoga and meditation intervention reduce anxiety and improve other clinical/p…
NCT07675226 — Bioequivalence Study of SKI-O-703 in Healthy Adults Under Fed Conditions
| Status | Not yet recruiting |
| Phase | Phase 1 |
| Sponsor | Oscotec Inc. |
| Enrollment | 48 |
| Study Type | INTERVENTIONAL |
| Conditions | Bioequivalence Study in Healthy Subjects; Immune Thrombocytopenia (ITP); Rheumatoid Arthritis (RA) |
| Interventions | ; |
This is an open-label, randomized, crossover Phase 1 study to evaluate the bioequivalence, pharmacokinetics, and safety of two oral SKI-O-703 drugs (test and reference) in healthy adults under fed conditions. Approximately 48 Korean and Caucasian participants will receive a single oral dose of the test drug and a single oral dose of the reference drug in a randomized sequence, separated by a wa…
NCT07684157 — A Phase IIa Study of JAB-8263 in Patients With Active Rheumatoid Arthritis
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | Jacobio Pharmaceuticals Co., Ltd. |
| Enrollment | 32 |
| Study Type | INTERVENTIONAL |
| Conditions | Rheumatoid Arthritis (RA) |
| Interventions | ; |
This study is an open-label, multi-center Phase IIa study. The study is divided into two phases. The first phase is a safety exploration phase. Participants with active rheumatoid arthritis were enrolled and treated with JAB-8263 alone for 4 weeks. The purpose is to evaluate the safety, PK/PD characteristics and preliminary effectiveness of JAB-8263 in participants with active RA.
NCT07671222 — Safety and Efficacy of Topical Infliximab in Autoimmune Dry Eye Disease
| Status | Not yet recruiting |
| Phase | Phase 2 |
| Sponsor | Instituto de Oftalmología Fundación Conde de Valenciana |
| Enrollment | 38 |
| Study Type | INTERVENTIONAL |
| Conditions | Sjogren Syndrome; Sjogren Syndrome With Keratoconjunctivitis; Dry Eye Disease (DED) |
| Interventions | ; |
Sjögren’s syndrome is a condition in which the immune system attacks the body’s moisture-producing glands. This often causes severe dry eye, leading to discomfort, irritation, blurred vision, and damage to the eye surface. Inflammation plays an important role in this process, and a protein called TNF-alpha is one of the key drivers.
This study will test a new eye drop containing infliximab, a …
Enrolling by Invitation
NCT07665086 — The Role of Isometric in Individuals With Rheumatoid Arthritis
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | Zülal TATAR |
| Enrollment | 66 |
| Study Type | INTERVENTIONAL |
| Conditions | Isometric Exercise; Pain; Oxygenation |
| Interventions |
The aim of this study is to investigate the acute effects of isometric exercise on pain modulation and muscle oxygenation in individuals with rheumatoid arthritis.
Completed Trials
NCT00055055 — Study of Families With Twins or Siblings Discordant for Rheumatic Disorders
| Status | Completed |
| Phase | N/A |
| Sponsor | National Institute of Environmental Health Sciences (NIEHS) |
| Enrollment | 1056 |
| Study Type | OBSERVATIONAL |
| Conditions | Rheumatoid Arthritis; Systemic Lupus Erythematosus; Idiopathic Inflammatory Myopathies |
This study will examine families in which one sibling of a sibling pair, or twin pair, has developed a systemic rheumatic disease and one has not, to see if and how the two differ in the following:
- Blood cell metabolism;
- Types of cells in the blood;
- Environmental exposures or genetic factors that might explain why one developed disease and the other did not.
Families in which one siblin…
NCT03915964 — A Study of Baricitinib (LY3009104) in Participants With Rheumatoid Arthritis
| Status | Completed |
| Phase | Phase 4 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 2659 |
| Study Type | INTERVENTIONAL |
| Conditions | Rheumatoid Arthritis |
| Interventions | ; |
This post-marketing study is designed to compare the safety of baricitinib versus tumor necrosis factor (TNF) inhibitors with respect to venous thromboembolic events (VTEs) when given to participants with rheumatoid arthritis.
NCT04196868 — Methotrexate and Metformin in Rheumatoid Arthritis Patients
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | University Hospital, Bordeaux |
| Enrollment | 128 |
| Study Type | INTERVENTIONAL |
| Conditions | Arthritis, Rheumatoid |
| Interventions | ; ; |
Methotrexate (MTX) is the anchor drug for patients with rheumatoid arthritis (RA). Despite its marked efficacy and acceptable side effect profile, about 1/3 of patients failed to reach RA remission. Metformin is the first-line therapy for type 2 diabetes. Its antioxidative and anti-inflammatory properties make it a good candidate for the treatment of inflammatory diseases such as rheumatoid art…
NCT05350072 — Two-arm Study to Assess Efficacy and Safety of Ianalumab (VAY736) in Patients With Active Sjogren’s Syndrome
| Status | Completed |
| Phase | Phase 3 |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 275 |
| Study Type | INTERVENTIONAL |
| Conditions | Sjogren Syndrome |
| Interventions | ; |
A randomized, double-blind, placebo controlled, 2-arm multicenter phase 3 study to assess the efficacy and safety of ianalumab in patients with active Sjogren’s syndrome (NEPTUNUS-1)
NCT07277491 — Assessment of Nutritional Status in Rheumatic Diseases and Association to Disease Activity
| Status | Completed |
| Phase | N/A |
| Sponsor | Cairo University |
| Enrollment | 460 |
| Study Type | OBSERVATIONAL |
| Conditions | Spondyloarthritis (SpA); Psoriatic Arthritis (PsA); Systemic Lupus Erythematous (SLE); Systemic Sclerosis (SSc); Rheumatoid Arthritis (RA |
The aim of the present work is to assess the nutritional status among different rheumatic diseases patients and to study its association with the corresponding diseases activity.
NCT05706493 — Association Between Periodontitis and the Level of Anti-citrullinated Protein Antibodies in Rheumatoid Arthritis
| Status | Completed |
| Phase | N/A |
| Sponsor | Misr International University |
| Enrollment | 62 |
| Study Type | OBSERVATIONAL |
| Conditions | Periodontal Diseases; Rheumatoid Arthritis |
the relationship between rheumatoid arthritis and periodontal disease is crucial and has been explained via a complex interplay of genetic, environmental, and hormonal factors that influence the host immune tolerance leading to both disease characteristics. The aim of this study is to clinically investigate the correlation between the levels of anti-citrullinated protein antibodies (ACPAs) in g…
Other (Withdrawn)
NCT02720874 — Multidisciplinary Approach for Treat To Target In Rheumatoid Arthritis
| Status | Withdrawn |
| Phase | N/A |
| Sponsor | Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center |
| Enrollment | N/A |
| Study Type | INTERVENTIONAL |
| Conditions | Arthritis, Rheumatoid |
| Interventions | ; ; |
This research will evaluate a multifaceted patient-centered intervention in a sample of socioeconomically disadvantaged Hispanic adults with rheumatoid arthritis (RA) that capitalizes on a partnership between the extended rheumatology healthcare team and each patient in order to promote understanding, uptake and adherence to the principles of treat-to-target strategy. The primary hypothesis of …