A Study to Evaluate the Efficacy and Safety of 608 in Adult Subjects With Active Ankylosing Spondylitis(AS)

Recruiting Phase 3 Interventional Study
Ankylosing Spondylitis
Pivotal Trial This treatment is in the last trial phase before FDA approval. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 3
Study type
Interventional
Purpose
Treatment
Participants needed
500 (estimated)
Sponsor
Sunshine Guojian Pharmaceutical (Shanghai) Co., Ltd. · Industry
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About This Trial

This study will evaluate the efficacy and safety of 608 in patients with AS.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Able to understand and comply with the protocol requirements, participate and sign the informed consent form (ICF) voluntarily; 2. At least 18 years of age at the time of signing the ICF, with no gender restrictions; 3. Meet the 1984 modified New York criteria for ankylosing …
Contacts

Qing hong Zhou

+86 18911301578

zhouqinghong@3sbio.com

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