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2 Years Prospective Study to Collect Real-life Data on the Retention, Quality of Life, Effectiveness and Treatment Pattern of Secukinumab in Adult Patients With Moderate to Severe Plaque Psoriasis, Psoriatic Arthritis, Ankylosing Spondylitis and Non-radiographic Axial Spondyloarthritis
Sponsor: Novartis Pharmaceuticals
Summary
This was an observational, prospective primary data collection study. The duration of observation was 2 years after study enrolment date. Disease and treatment history were retrospectively reviewed from medical record at enrollment with no time limits for the key diagnosis of enrolment (plaque psoriasis, psoriatic arthritis, ankylosing spondylitis and non-radiographic axial spondyloarthropathy).
Official title: 2 Years Prospective Study to Collect Real-life Data On the Retention, Quality of Life, Effectiveness and Treatment Pattern of Secukinumab in Adult Patients With Moderate to Severe Plaque Psoriasis, Psoriatic Arthritis, Ankylosing Spondylitis and Non-radiographic Axial spondyloarthriTis (PROMPT)
Key Details
Gender
All
Age Range
18 Years - 80 Years
Study Type
OBSERVATIONAL
Enrollment
127
Start Date
2022-03-25
Completion Date
2025-08-20
Last Updated
2026-10-23
Healthy Volunteers
No
Conditions
Interventions
secukinumab
Prospective observational study. There is no treatment allocation. Patients who are receiving or intend to receive secukinumab are eligible to enroll into this study.
Locations (10)
Novartis Investigative Site
Songkhla, Hat Yai, Thailand
Novartis Investigative Site
Muang, Thailand, Thailand
Novartis Investigative Site
Khon Kaen, THA, Thailand
Novartis Investigative Site
Bangkok, Thailand
Novartis Investigative Site
Bangkok, Thailand
Novartis Investigative Site
Bangkok, Thailand
Novartis Investigative Site
Bangkok, Thailand
Novartis Investigative Site
Chiang Mai, Thailand
Novartis Investigative Site
Kaen, Thailand
Novartis Investigative Site
Nakhon Ratchasima, Thailand