Ankylosing spondylitis (AS) is a chronic inflammatory arthritis that primarily targets the spine and sacroiliac joints, causing progressive pain, stiffness, and in severe cases fusion of vertebrae. It typically begins in young adults and is strongly associated with the HLA-B27 gene. Without effective treatment, spinal mobility can be severely restricted over time.
What's actually going on in research
TNF inhibitors and IL-17 inhibitors (secukinumab, ixekizumab) are now well-established treatments that significantly reduce inflammation and improve function in active AS, and both classes have demonstrated benefits for radiographic progression. JAK inhibitors such as upadacitinib are now also approved and offer an oral alternative. Trials are exploring IL-23 inhibitors, which showed mixed initial results in AS despite effectiveness in related conditions, as well as biomarker-driven approaches to personalize therapy selection.
JAK inhibitor options
Oral JAK inhibitors, including upadacitinib and filgotinib, are approved or in late-phase trials for AS, offering patients an effective oral alternative to injectable biologics.
IL-23 inhibitor research
Despite limited results in axial spondyloarthritis so far, trials continue investigating whether specific patient subgroups defined by biomarkers respond to IL-23 pathway blockade.
Treat-to-target strategies
Studies are evaluating whether targeting low disease activity or remission — and adjusting therapy accordingly — improves long-term spinal outcomes and quality of life compared to symptom-guided treatment.
What to know before you search
Eligibility typically requires confirmed axial spondyloarthritis diagnosis, active disease despite NSAIDs, and no prior or current use of the specific biologic being studied.
What types of trials are currently open
- JAK inhibitor trials — Comparing oral JAK inhibitors to biologics in active ankylosing spondylitis across diverse patient populations.
- Biologic therapy trials — Testing new IL-17 and IL-23 pathway inhibitors and combination strategies in active disease.
- Early intervention studies — Evaluating whether prompt treatment delays radiographic spinal fusion in newly diagnosed patients.
- Treat-to-target trials — Assessing structured remission-targeting approaches versus standard symptom management.
- Biomarker studies — Identifying imaging and blood markers to predict treatment response and disease progression.
Recently added Ankylosing Spondylitis trials
Exploratory Investigation of the Acceptance and Utility of 14-day Trial Periods and Application-related Outcome Measurement (AbEM) Within the Routine Prescription of the DiGA Axia.
This prospective, multicenter, controlled real-world quality management study explores the acceptance and utility of two measures discussed in the context of the German Digital Act (DigiG) for the digital health application (DiGA) Axia: a 14-day trial period and an application-related outcome measurement (AbEM). Patients with axial spondyloarthritis in Axia's indication area who are eligible for prescription in routine care will receive one of two onboarding brochure versions in a 1:1 allocation: either the standard access procedure or immediate 14-day trial access until the health insurance activation code arrives. The manufacturer will analyze aggregated anonymized data to compare voucher redemption and app activation frequencies between groups and to assess acceptance and return rates of a voluntary five-item AbEM questionnaire at weeks 6 and 12. Secondary analyses will descriptively evaluate AbEM results and anonymized usage data.
Evaluating the Efficacy and Short-Term Prognosis of Integrated Traditional Chinese and Western Medicine for Ankylosing Spondylitis(AS): A Protocol for a Cohort Study
This study is a multicenter, prospective cohort study designed to systematically evaluate the clinical efficacy of integrated Traditional Chinese and Western Medicine on short-term functional improvement in patients with ankylosing spondylitis, with the Bath Ankylosing Spondylitis Functional Index (BASFI) at 6 months of treatment as the primary outcome measure.
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