Condition: Rheumatoid Arthritis · Sponsor: Changchun GeneScience Pharmaceutical Co., Ltd.
This is a multicenter, randomized, double-blind, parallel, placebo- and active comparator- controlled clinical study conducted in patients with moderately to severely active RA and an inadequate response to at least one DMARD, designed to assess the efficacy and safety of GenSci120 injection in this patient population. The study consists of a screening period (≤ 4 weeks), a placebo-controlled treatment period (14 weeks), an extension treatment period (14 weeks), and a follow-up period (10 weeks), with a total of 17 scheduled visits.
This description comes directly from the study's public registry record.
Wei WANG · +86 18201085833 · wangwei13@genscigroup.com
Xi DENG · +86 18201085833 · dengxi@genscigroup.com
Always discuss trial participation with your own doctor first.
| Peking University People's Hospital | Beijing, Beijing Municipality, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07423533