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EULAR 2025 Insights Corner: Psoriatic Arthritis Highlights, Competitor Landscape & Biosimilars

Insights Details

Month: July 25

Tags: Eular, Conference, Pre-clinical, Phase 1, Phase 2, Phase 3, US FDA, EMA, Company Profile, Product profile, Psoriatic Arthritis, Market Trends, Landscape, Deal Analysis, Funding Analysis, Clinical trials, Biosimilar, Europe, Clinical trials

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About topic:

EULAR 2025 promotes a “hit hard and early” treat-to-target strategy in high-risk psoriatic arthritis (PsA) among other immunology indications, using frequent assessment and rapid therapy escalation to achieve remission or low disease activity. In Europe this strategy is enabled by a wide range of approved biologic and targeted synthetic DMARDs acting on TNF, IL17, IL23, JAK, and TYK2, with more TYK2 inhibitors and IL17focused agents in late-stage development. For Insights Corner we particularly focused on PsA although the EULAR focused on all the immunology indications including rare and orphans

EULAR 2025 Insights Corner: Psoriatic Arthritis Highlights, Competitor Landscape & Biosimilars

Highlights:

A “treat early and intensively” approach in high‑risk PsA, with trials like SPEED indicating that starting TNF inhibitors early can provide sustained benefit out to 48 weeks
The PsA market is moving beyond a TNF‑centric model toward IL‑17, TYK2, and novel nanobody therapies as key differentiators, while biosimilars and EU cost pressures push companies to prove clinical value and optimize lifecycle strategies
There is a strong drive toward precision medicine using biomarkers, synovial and advanced imaging (whole‑body PET/MRI), plus AI tools to enable earlier diagnosis, better risk stratification, and personalized monitoring
From 2024–2025 PsA deal‑making has surged, including licensing and co‑promotion deals (such as Samsung Bioepis partnerships) and MoonLake’s financing to advance sonelokimab, which in the ARGO phase 2 trial showed strong multidomain efficacy and tolerability, underpinning ongoing phase 3 IZAR studies