Study of Efficacy and Safety of Secukinumab in Japanese Patients With Active Ankylosing Spondylitis

PHASE3CompletedINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

March 22, 2016

Primary Completion Date

July 5, 2017

Study Completion Date

May 16, 2018

Conditions
Ankylosing Spondylitis
Interventions
DRUG

Secukinumab 150 mg provided in 1.0 mL pre-filled syringes (PFSs) for sc injection.

Baseline, 1, 2, 3, 4 week. After 4 week, administered every 4 weeks.

Trial Locations (10)

807-8556

Novartis Investigative Site, Kitakyushu

761-0793

Novartis Investigative Site, Kita-gun

783 8505

Novartis Investigative Site, Nankoku

632-8552

Novartis Investigative Site, Tenri

700-0013

Novartis Investigative Site, Okayama

586-8521

Novartis Investigative Site, Kawachi-Nagano

565 0871

Novartis Investigative Site, Suita

113-8431

Novartis Investigative Site, Bunkyo Ku

104-8560

Novartis Investigative Site, Chuo Ku

160-0054

Novartis Investigative Site, Shinjuku-ku

Sponsors
All Listed Sponsors
lead

Novartis Pharmaceuticals

INDUSTRY