YANTAI, China - RemeGen Co., Ltd. ('RemeGen' or 'the Company') (9995.HK, SHA: 688331), a commercial-stage biotechnology company, recently announced the preliminary results of the Phase III confirmatory study of its proprietary novel fusion protein Telitacicept for the treatment of systemic lupus erythematosus (SLE) in China.

The study included 335 patients who were randomized to weekly subcutaneous injections of Telitacicept (160 mg) or placebo in combination with standard therapy for 52 weeks. Preliminary results from the full analysis set (FAS) showed that at week 52, patients who received Telitacicept had a significantly higher rate of SRI-4 (The Systemic Lupus Erythematosus Responder Index 4) response than those who received placebo (82.6% vs. 38.1%, p

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