Efficacy and Influencing Factors of Secukinumab in Patients With Axial Spondyloarthritis

NCT07130331 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2025-08-19

No results posted yet for this study

Summary

This study aimed to explore the efficacy and influencing factors of secukinumab in axSpA patients by conducting a real-world retrospective analysis.

Conditions

  • Axial Spondylarthritis (axSpA)
  • Secukinumab

Interventions

DRUG

Secikinumab

secukinumab 150 mg at weeks 0, 1, 2, 3, and 4, followed by 150 mg s.c. every 4 weeks

Sponsors & Collaborators

  • The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-06-01
Primary Completion
2024-07-01
Completion
2025-08-01

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07130331 on ClinicalTrials.gov