EICHORCondition: Rheumatoid Arthritis (RA) · Sponsor: Hangzhou Highlightll Pharmaceutical Co., Ltd
This is a randomized, double-blind, placebo-controlled parallel-group Phase II study. The study aims to evaluate the efficacy and safety of TLL-018 in adult patients with moderate to severe active rheumatoid arthritis who have inadequate response or intolerance to conventional synthetic disease-modifying antirheumatic drugs (csDMARDs).
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| Peking Union Medical College Hospital, Chinese Academy of Medical Sciences | Beijing, Beijing Municipality, China | — |
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Source record: clinicaltrials.gov/study/NCT07748728