The Clinical Efficacy and the Changes of Immune Cells Subsets With Bioagents in Ankylosing Spondylitis Patients

PHASE4Active, not recruitingINTERVENTIONAL
Enrollment

100

Participants

Timeline

Start Date

March 15, 2022

Primary Completion Date

December 31, 2024

Study Completion Date

December 31, 2024

Conditions
Ankylosing Spondylitis
Interventions
DRUG

Secukinumab 150 mg/ml

Secukinumab 150 mg will be administered at Baseline, Week 1, 2, 3, 4, 6, 8 followed by dosing every 4 weeks until Week 24

DRUG

Adalimumab Ab

adalimumab biosimilar 40 mg will be administered at Baseline followed by dosing every 2 weeks until Week 24

DRUG

NSAID

stable dose

DRUG

Thalidomide Pill

If patients have inadequate response to bioagents, thalidomide 50 mg will be administered at 12 week followed by dosing everyday until Week 24.

Trial Locations (1)

250012

Qilu Hospital, Jinan

All Listed Sponsors
lead

Qilu Hospital of Shandong University

OTHER