Arthritis, Psoriatic

15

Review clinical trials related to Arthritis, Psoriatic. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Evaluation of Sonelokimab in Patients With Active Psoriatic Arthritis and Anti-TNFα Inadequate Response

This is a study to confirm the clinical efficacy and safety of sonelokimab compared with placebo in the treatment of adults with active psoriatic arthritis who have had a previous inadequate response or intolerance to anti-tumor necrosis factor (TNF)α therapy.

Participants needed: 600
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: MoonLake Immunotherapeutics AGUpdated: Jul 13, 2026Locations: 139
Eligibility criteria

Participants must be ≥18 years of age . [+5]

Participants with a known hypersensitivity to sonelokimab or any of its excipien... [+7]

Status: Not yet recruiting

A Study to Assess Concentration of TREMFYA in Breast Milk of Lactating Women Who Are Receiving TREMFYA Therapeutically

The purpose of this post-marketing study is to assess the amount of guselkumab in breast milk of lactating women receiving guselkumab as part of their standard clinical care provided by their treating physician, for any of the approved indications.

Participants needed: 10
Trial details
Phase: Phase 4Age: 18+Biological sex: FemaleType: InterventionalSponsor: Janssen Research & Development, LLCUpdated: Jun 17, 2026Locations: 1
Eligibility criteria

Has an active diagnosis of at least one approved indication for guselkumab (psor... [+6]

Has any current or previous illness that, in the opinion of the investigator, mi... [+4]

Status: Recruiting

Evaluation of Sonelokimab in Patients With Active Psoriatic Arthritis and Anti-TNFα Inadequate Response

This is a study to confirm the clinical efficacy and safety of sonelokimab compared with placebo in the treatment of adults with active psoriatic arthritis who have had a previous inadequate response or intolerance to anti-tumor necrosis factor (TNF)α therapy.

Participants needed: 600
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: MoonLake Immunotherapeutics AGUpdated: Jun 12, 2026Locations: 138
Eligibility criteria

Participants must be ≥18 years of age . [+5]

Participants with a known hypersensitivity to sonelokimab or any of its excipien... [+7]

Status: Recruiting

A Long-term Extension (LTE) Study of Guselkumab in Pediatric Participants

The purpose of this study is to evaluate long-term safety of subcutaneous guselkumab in pediatric participants with moderately to severely active ulcerative colitis, or moderately to severely active Crohn's disease, or juvenile psoriatic arthritis (jPsA).

Participants needed: 196
Trial details
Phase: Phase 3Age: 3+Biological sex: AllType: InterventionalSponsor: Janssen Research & Development, LLCUpdated: Jun 11, 2026Locations: 47
Eligibility criteria

Must have completed the dosing planned in the primary pediatric guselkumab study [+3]

Participant is greater than or equal to (>=) 18 years of age and resides in a co... [+5]

Status: Recruiting

A Study of Guselkumab Treatment Persistence in Psoriatic Arthritis Participants

This observational study aims to assess the 1-year persistence of guselkumab in adult patients with psoriatic arthritis (an inflammatory disease that affects the joints in participants with psoriasis, a skin condition that causes red, scaly patches).

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Janssen-Cilag Ltd.Updated: Jun 5, 2026Locations: 1
Eligibility criteria

Have a confirmed diagnosis of psoriatic arthritis (PsA) as determined by a rheum... [+4]

Have already taken a specific interleukin-23 inhibitor (IL-23i) treatment. [+6]

Status: Recruiting

A Study to Evaluate the Efficacy and Safety of JNJ-88545223 for the Treatment of Participants With Active Psoriatic Arthritis

The purpose of this study is to evaluate how well the study drug JNJ-88545223 works compared with a placebo (an inactive substance) in adults with active psoriatic arthritis (PsA). The study aims to see whether treatment with JNJ-88545223 can help reduce the signs and symptoms of PsA and improve joint and skin health.

Participants needed: 240
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Janssen Research & Development, LLCUpdated: Jun 5, 2026Locations: 68
Eligibility criteria

Have a diagnosis of psoriatic arthritis (PsA) for at least 3 months before the f... [+4]

Has a nonplaque form of psoriasis (for example, erythrodermic, guttate, or pustu... [+4]

Status: Recruiting

A Study of Guselkumab in Participants With Psoriatic Arthritis (PsA) in a Real-World Setting

The purpose of this study is to assess how well guselkumab works in improving symptoms of psoriatic arthritis (an inflammatory disease that affects the joints in participants with psoriasis, a skin condition that causes red, scaly patches) using muscoloskeletal ultrasound (MSUS) in a real-world setting.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Janssen Research & Development, LLCUpdated: Jun 5, 2026Locations: 21
Eligibility criteria

Diagnosis of PsA as per CASPAR classification criteria for at least six months w... [+4]

Previous exposure to Guselkumab or to more than one bDMARD for any indications [+4]

Status: Recruiting

A Study of Guselkumab Administered Subcutaneously in Treatment of Indian Participants With Psoriatic Arthritis (PsA)

The purpose of this study is to evaluate the safety and how well guselkumab treatment works (efficacy) in participants with psoriatic arthritis (PsA; a chronic, autoimmune form of arthritis that causes joint inflammation) who had inadequate response to standard therapies.

Participants needed: 100
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: Johnson & Johnson Private LimitedUpdated: Jun 5, 2026Locations: 10
Eligibility criteria

Participants who have definite diagnosis of active psoriatic arthritis (PsA) (ac... [+9]

History of latent or active granulomatous infection prior to screening [+4]

Status: Recruiting

A Study to Evaluate the Efficacy and Safety of Icotrokinra (JNJ-77242113) in Biologic-experienced and Biologic-naive Participants With Active Psoriatic Arthritis

The purpose of this study is to evaluate the efficacy of icotrokinra (JNJ-77242113) compared to placebo in biologic-experienced and biologic-naive participants with active psoriatic arthritis (PsA) by assessing the reduction in signs and symptoms of PsA.

Participants needed: 750
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Janssen Research & Development, LLCUpdated: Jun 5, 2026Locations: 216
Eligibility criteria

Have active psoriatic arthritis (PsA) despite current or previous use of greater... [+5]

Has a history or current signs or symptoms of severe, progressive, or uncontroll... [+4]

Status: Recruiting

Pain in Inflammatory Joint Diseases

Our primary objective is to better understand the etiology and consequences of chronic paint by using an explorative approach to identify phenotypes and endotypes of patients with inflammatory joint diseases, with a special focus on central sensitization and cognitive functioning as a key element in chronic pain. We will also examine the risk factors and clinical impact of these factors on pain, disease activity and treatment effects in a longitudinal study of patients with inflammatory joint disesases.

Participants needed: 350
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Diakonhjemmet HospitalUpdated: Apr 13, 2026Locations: 1
Eligibility criteria

All patients who initiate or switch biological or targeted synthetic DMARDs

None

Status: Recruiting

Effects of Phytocannabinoids on Immune Response and Autophagy During Chronic Immune-mediated Inflammatory Diseases

Cannabis, in addition to its psychotropic properties, could have anti-inflammatory and immunomodulatory effects. Phytocannabinoids (pCBs) are a group of molecules naturally secreted by the cannabis plant. The major pCBs are cannabidiol (CBD) and Δ9-tetrahydrocannabinol Δ9 (THC). Only THC has psychotropic effects, which CBD does not have. Alongside these two main components, there is a wide variety of other molecules, such as other pCBs and terpenes which could increase the effects on immune system through synergistic interactions between these different compounds ("entourage effect").In vivo, pCBs essentially interfere with the endocannabinoid system, acting on many ubiquitous receptors, present on a significant number of different cell types. Numerous published studies show that pCBs have immunomodulatory and anti-inflammatory properties by acting on several of these receptors, whether through modulation of the immune response of different cell types, effects on cytokine networks, reduction of innate and adaptive responses and/or impact on cell survival or death (autophagy, proliferation/ apoptosis). The Immune-Mediated Inflammatory Diseases (IMIDs) affect 5 to 7% of the general population in Western countries, involve different organs (joints, skin, digestive tract) but share the same inflammatory mechanisms resulting from a dysregulation of the immune response. Our research focuses on the identification of the most effective phytochemical profile of pCBs, allowing an optimal effect on chronic inflammatory pathologies of interest among immune-mediated chronic inflammatory diseases (IMIDs). The pCB-IMIDs project is therefore part of an innovative translational project, around new therapeutic applications of medical cannabis (CannAppIMIDs). In our study, we will include 100 patients with one of IMIDs among Rheumatoid Arthritis, spondylarthritis, psoriatic arthritis, Sjogren disease and systemic lupus, at different stage and with different treatments. After patient's consent we will collect for research purposes an additional 40 ml of blood during a routine care blood test. Mononuclear and polynucleated blood cells will be exposed in vitro to different full-spectrum pCB extracts (full spectrum extract) including a CBD dominant and low THC extract (\<0.2%), 1 dominant THC extract, 1 balanced THC/CBD extract and 1 dominant CBG extract. In this cross-sectional study, our objective will be to assess the biological effects of different pCB compositions on inflammatory profiles (concentrations of pro and anti-inflammatory cytokines and chemokines) and modulations of expression profiles (autophagy, apoptosis, and cannabinoid receptor expression profile).

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Centre Hospitalier Régional d'OrléansUpdated: Dec 30, 2025Locations: 1
Eligibility criteria

Male or female ≥ 18 years old [+4]

Patient who received intravenous corticosteroid therapy less than 4 weeks ago [+4]

Status: Recruiting

Influence of Sodium Intake in spondyLoarthriTes

The aim of the SALT study is to analyze the relationship between dietary sodium intake and disease activity in patients with axial spondyloarthritis (radiographic or non-radiographic) or psoriatic arthritis.

Participants needed: 250
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Centre Hospitalier Universitaire de BesanconUpdated: Jul 9, 2025Locations: 4
Eligibility criteria

patients with axial spondyloarthritis (radiographic or non-radiographic) or psor... [+1]

patient treated by cyclosporine, diuretics, angiotensin-converting enzyme inhibi... [+3]

Status: Recruiting

Characterization of Immunogenicity of TNF Inhibitors in Arthritis Patients With Poorer Treatment Response.

The aim of the study is to explore whether the influence of gender, tobacco smoking and obesity on treatment response in tumor necrosis factor inhibitors (TNFIs) can be explained by high degree of inflammation, human leucocyte antigen (HLA) type, autoantibodies, TNF and TNFI concentration and presence of ADA.

Participants needed: 120
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Aalborg University HospitalUpdated: Jun 28, 2024Locations: 1
Eligibility criteria

Patients > 18 years [+4]

Status: Recruiting

IMPACT - AndHealth Autoimmune Research Registry

This is a patient research registry aimed at evaluating the effectiveness of a comprehensive, root-cause medical approach ("AndHealth program") for autoimmune disorders. This approach involves a combination of pharmacological and non-pharmacological therapies offered under the care of a licensed physician with the support of health coaches. While protocol guidance is provided, the therapeutic approach is personalized to the individual needs of patients. The autoimmune disorders of focus in this registry include rheumatoid arthritis, psoriatic arthritis, psoriasis and ankylosing spondylitis. A variety of validated labs, patient-reported outcomes, and medication usage will be assessed among participating patients over a period of up to five years to evaluate the long-term effectiveness of this approach.

Participants needed: 2,500
Trial details
Age: 18-70Biological sex: AllType: ObservationalSponsor: AndHealthUpdated: Jun 29, 2023Locations: 1Duration: 5 Years
Eligibility criteria

Adults 18 to 70 years of age [+3]

Pregnant, breastfeeding, or planning to become pregnant in the next 12 months [+6]

Status: Recruiting

Novel Complex Radiodiagnostics of Peripherial Arthropathies

Chronic peripherial arthritides are common diseases with soaring public health consequences. Our goal is to assess the role of photon-counting detector computed tomography in the diagnostics of peripherial arthropathies.

Participants needed: 500
Trial details
Age: 18-100Biological sex: AllType: ObservationalSponsor: Semmelweis UniversityUpdated: Dec 20, 2022Locations: 3
Eligibility criteria

Rheumatoid arthritis (EULAR/ACR Criteria) / Psoriatic arthritis (CASPAR Criteria... [+1]

age: <18 years, > 100 years [+2]