Efficacy and Safety Study of Secukinumab in Chinese Participants With Non-radiographic Axial Spondyloarthritis

PHASE3CompletedINTERVENTIONAL
Enrollment

138

Participants

Timeline

Start Date

July 21, 2021

Primary Completion Date

April 3, 2024

Study Completion Date

February 14, 2025

Conditions
Non-radiographic Axial Spondyloarthritis
Interventions
DRUG

Secukinumab

Secukinumab 150 mg s.c. at BSL, Weeks 1, 2, and 3, followed by administration every 4 weeks starting at Week 4.

DRUG

Placebo

Placebo 150 mg s.c.at BSL, Weeks 1, 2 and 3, followed by administration every 4 weeks starting at Week 4.

Trial Locations (29)

100000

Novartis Investigative Site, Beijing

100044

Novartis Investigative Site, Beijing

100050

Novartis Investigative Site, Beijing

130021

Novartis Investigative Site, Changchun

150000

Novartis Investigative Site, Harbin

200040

Novartis Investigative Site, Shanghai

200050

Novartis Investigative Site, Shanghai

210008

Novartis Investigative Site, Nanjing

210009

Novartis Investigative Site, Nanjing

225001

Novartis Investigative Site, Yangzhou

230001

Novartis Investigative Site, Hefei

230601

Novartis Investigative Site, Hefei

233004

Novartis Investigative Site, Bengbu

276000

Novartis Investigative Site, Linyi

300052

Novartis Investigative Site, Tianjin

315016

Novartis Investigative Site, Zhejiang

325000

Novartis Investigative Site, Wenzhou

330006

Novartis Investigative Site, Nanchang

337000

Novartis Investigative Site, Pingxiang

361001

Novartis Investigative Site, Xiamen

410011

Novartis Investigative Site, Changsha

430030

Novartis Investigative Site, Wuhan

510080

Novartis Investigative Site, Guangzhou

510515

Novartis Investigative Site, Guangzhou

515041

Novartis Investigative Site, Shantou

518020

Novartis Investigative Site, Shenzhen

650000

Novartis Investigative Site, Kunming

830001

Novartis Investigative Site, Ürümqi

014010

Novartis Investigative Site, Baotou

Sponsors
All Listed Sponsors
lead

Novartis Pharmaceuticals

INDUSTRY