drugset / Trial / NCT06011889
Study of the Efficacy and Safety of Etanercept Treatment in Patients With SAPHO Syndrome
Phase 2/3
Recruiting
60 enrolled
National Institute of Geriatrics, Rheumatology and Rehabilitation, Poland
Medical Research Agency, Poland · collab
RandomizedParallel-groupDouble-blindTreatment
Summary
The study includes adult patients with SAPHO syndrome (ORPHA: 793), meeting the modified classification criteria according to Kahn (2003), with the ineffectiveness of standard treatment (patient's global assessment of the disease on the VAS scale greater than or equal to 4 cm with accompanying pain on the VAS scale greater than or equal to 4 cm) treated with non-steroidal anti-inflammatory drugs in a stable dose for at least 4 weeks and/or classical disease-modifying antirheumatic drugs in stable doses for at least 12 weeks.
Timeline
- Start
- 2024-09-04
- Primary completion
- 2028-10-18
- Completion
- 2028-10-18
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Etanercept | Protein / enzyme biologic | — | — |