Psoriatic arthritis affects about 30% of people with psoriasis, causing joint pain, stiffness, and sometimes permanent damage if untreated. Treatment has expanded rapidly over the past decade, with more than a dozen biologics and oral medications now available that can stop joint damage and clear skin in many people.
What's actually going on in research
Trials are testing IL-23 inhibitors, JAK inhibitors, and TYK2 inhibitors that may work faster or stay effective longer than current drugs. Researchers are also studying whether early aggressive treatment can prevent joint damage before it starts, and testing oral drugs that combine convenience with strong disease control.
TYK2 inhibitors
Deucravacitinib, an oral TYK2 inhibitor FDA-approved in 2022, works differently from JAK inhibitors and may carry fewer safety concerns. Additional TYK2 inhibitors are in trials to see if they match this profile.
Treat-to-target strategies
Studies are testing whether adjusting treatment aggressively to reach specific goals prevents more joint damage than standard care. Early data suggest this approach may preserve joint function better.
Dual inhibitors
New drugs targeting two inflammatory pathways at once are in trials. The goal is stronger disease control without simply adding more medications.
What to know before you search
Eligibility typically depends on number of swollen and tender joints, prior treatment history, and whether current medication has stopped working or caused side effects.
What types of trials are currently open
- Treatment trials — Testing new biologics or oral medications to see if they control joint symptoms and skin disease better than current options.
- Head-to-head trials — Comparing two active treatments directly to see which works faster, lasts longer, or has fewer side effects.
- Early intervention trials — Testing whether starting strong treatment early in disease can prevent permanent joint damage.
- Switching studies — Testing what happens when people switch from one biologic to another, and whether new drugs work in people who've stopped responding to older ones.
- Imaging studies — Using ultrasound or MRI to see if new treatments reduce inflammation inside joints that looks quiet on the outside.
Recently added Psoriatic Arthritis trials
Take an experimental drug designed to reduce psoriatic arthritis symptoms
The purpose of this Phase 2a/b study is: 1. to evaluate the efficacy, safety and tolerability of DDY391 in participants with psoriatic arthritis (PsA). 2. to determine the dose-response relationship of DDY391 in participants with PsA to support dose selection for Phase 3.
Take a new immune therapy designed for psoriatic arthritis
Psoriatic arthritis (PsA), a chronic immune-mediated heterogeneous inflammatory disease characterized by musculoskeletal inflammation (arthritis, enthesitis, spondylitis and dactylitis), usually occurs in patients with psoriasis. The spondyloarthritides (SPs) (of which psoriasis is one) are a group of inflammatory diseases that share an association with the HLA-B27 MHC class I molecule. Given this association, these diseases are classically regarded as disorders of adaptive immunity. In bone marrow donation, HLA-B exon 1 dimorphism (HLAB leader) is associated with risk of graft- versus-host disease, relapse and overall survival after unrelated hematopoietic cell transplantation (UHCT), haploidentical UHCT and cord transplantation. In the literature, there are no studies suggesting the involvement of the HLA B leader gene in MS and RPs. The main aim of this study is to compare the presence of the HLA B leader gene between a group of patients with psoriatic arthritis and a healthy group without inflammatory disease.
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