Efficacy and Safety of Telitacicept in the Treatment of Refractory Rheumatoid Arthritis

The requested reference [156c3d625a43d01f09a7f300654fb6fc8c36689c] no longer exists in our database. It has been replaced by the current reference: [78aa7070e86b3911a58cde072b2f3b7f6132c9fd]

Authors
Category Primary study
Registry of TrialsClinicalTrials.gov
Year 2026
The refractory rheumatoid arthritis is a heterogeneous subgroup of RA patients, whosedisease has not been satisfactorily controlled with several lines of DMARDs using thetreat‐to‐target strategy. In 2024, telitacicept was approved for the treatment ofrheumatoid arthritis in China, and several case reports have demonstrated its efficacy inrefractory RA.This study plans to enroll 420 adult patients with difficult‐to‐treat rheumatoidarthritis, randomized in a 1:1 ratio to receive either telitacicept (160mg qw) plusstandard therapy or standard therapy alone for 24 weeks.
Epistemonikos ID: 94f57baceac9d4005777f4b3cdd80ba758ef2503
First added on: Sep 01, 2026