SBP GROUP (01177.HK): Preclinical Data of Oral STAT6 Degrader TQH5528 Presented at ERS 2026

On 8 September 2026, Sino Biopharmaceutical Limited (01177.HK) announced in a voluntary announcement that preclinical data of TQH5528, an oral STAT6 degrader independently developed by subsidiary Chia Tai-Tianqing Pharmaceutical Group, had been presented at ERS 2026, showing picomolar-level STAT6 degradation superior to comparator KT-621, significant STAT6 downregulation after a single dose in non-human primates, and improved airway hyperresponsiveness in a humanised asthma mouse model, with in vivo safety studies ongoing.

NewTimeSpace News: On 8 September 2026, Sino Biopharmaceutical Limited (stock code: 01177) issued a voluntary announcement stating that preclinical study data of TQH5528, an oral STAT6 degrader independently developed by its subsidiary Chia Tai-Tianqing Pharmaceutical Group Co., Ltd., had been presented as an oral presentation at the European Respiratory Society International Congress 2026 (ERS 2026), together with an accompanying e-poster.

According to the announcement, TQH5528 is an oral STAT6 degrader developed on a proprietary oral protein degrader technology platform (OAPD) with global intellectual property rights. It targets the IL-4/IL-13/STAT6 signalling axis and exerts efficacy through a protein degradation mechanism, with potential to become a next-generation therapy that is more convenient to administer than injectable biologics. The molecule features a novel CRBN ligand structure with no IMiD-related activity, picomolar-level potent STAT6 degradation activity, superior inhibition of the IL-4/IL-13 pathway versus comparator molecule KT-621, and good oral exposure and bioavailability across multiple species.

Preclinical data showed that in in vitro cell assays, TQH5528 demonstrated stronger activity than KT-621 and dupilumab in degrading STAT6 protein, inhibiting pSTAT6 and suppressing downstream inflammatory cytokine release. In non-human primate studies, a single dose achieved significant STAT6 downregulation, daily multiple dosing achieved complete STAT6 degradation in blood within four hours, and low doses achieved more than 95% STAT6 degradation in tissues such as the spleen, lung and peripheral blood mononuclear cells. In an HDM-induced IL-4/IL-4R humanised asthma mouse model, the product significantly improved airway hyperresponsiveness, reduced peripheral inflammatory cells and improved eosinophil infiltration; in vivo safety studies are ongoing.

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