Registro de fonte primária

Nível de decisãoResultados topline

Monte Rosa Therapeutics Reports Positive GFORCE-1 Phase 1 Topline for MRT-8102 in ASCVD Risk Subjects

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).

Fatos principais

Arquivado
1 de out. de 2026, 11:38
Evento
Resultados topline
Direção
Positivo
Fonte
SEC 8-K
Confiança
Com fonte
Redução de SAA
51%
Redução de IL-6
54%
Redução de HMGB1
40% (quartil superior)
Redução de IL-1b
37% (quartil superior)
Redução de hsCRP
85%
Degradação de NEK7
redução mediana de 80-90%
Redução de S100A12
46%
Redução de fibrinogénio
28%
Redução de calprotectina
56%
Redução de lipoproteína a
24%

Trecho da fonte

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

SEC 8-K

Monte Rosa Therapeutics Reports Positive GFORCE-1 Phase 1 Topline for MRT-8102 in ASCVD Risk Subjects | SimianX AI