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NCT07748728 — "TLL-018 in Patients With Moderate to Severe Active Rheumatoid Arthritis With Inadequate Response or Intolerance to csDMARDs" trial site landscape

Public-registry site landscape for NCT07748728, “TLL-018 in Patients With Moderate to Severe Active Rheumatoid Arthritis With Inadequate Response or Intolerance to csDMARDs”, a Rheumatoid Arthritis (RA) study sponsored by Hangzhou Highlightll Pharmaceutical Co., Ltd. All data below is from public sources; Eichor is not affiliated with the sponsor.

TrialNCT07748728 (registry record)
Study titleTLL-018 in Patients With Moderate to Severe Active Rheumatoid Arthritis With Inadequate Response or Intolerance to csDMARDs
Official titleA Randomized, Double-Blind, Placebo-Controlled Parallel-Group Phase II Study to Evaluate the Efficacy and Safety of TLL-018 in Patients With Moderate to Severe Active Rheumatoid Arthritis With Inadequate Response or Intolerance to csDMARDs
SponsorHangzhou Highlightll Pharmaceutical Co., Ltd
Condition(s)Rheumatoid Arthritis (RA)
PhasePHASE2
Listed sites1
Intervention(s)TLL-018, Placebo
Site countriesChina

Patient-friendly overview of this study: eichor.com/study/NCT07748728.

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