บันทึกจากแหล่งปฐมภูมิ
MRT-8102 achieved robust NEK7 degradation and normalized multiple key ASCVD pathogenic drivers (DAMPs, IL-1β, hsCRP, fibrinogen, Lp(a)) to healthy-volunteer levels in obese subjects with elevated CVD risk. The asset was safe and well-tolerated with no SAEs or increased infection risk. This topline outcome informs dose selection and enables planned Phase 2 starts in coronary artery disease (GFORCE-2, H1 2027), gout (GEMINI-1, Q4 2026/Q1 2027), and hidradenitis suppurativa (GALAXY-1, H1 2027).
EX-99.1 2 glue-ex99_1.htm EX-99.1 EX-99.1 Exhibit 99.1 Monte Rosa Therapeutics Announces Positive Results for MRT-8102 in GFORCE-1 Phase 1 Study Showing Normalization of Key Pathogenic Drivers of ASCVD in Subjects with Elevated CVD Risk In obese subjects at elevated cardiovascular disease (CVD) risk, MRT-8102, a NEK7-directed molecular glue degrader in development for the treatment of NLRP3/IL-1-driven inflammatory diseases, normalized multiple atherosclerotic cardiovascular disease (ASCVD) pathogenic drivers of local plaque inflammation, thrombosis, and systemic inflammation Robust and sustained NEK7 degradation observed across 5 mg, 20 mg, and 40 mg once-daily dose levels, with similar biomarker reductions at all three doses HMGB1, calprotectin, S100A12, and SAA, damage-associated mol