Monte Rosa Therapeutics to Present Results of MRT-8102 GFORCE-1 Phase 1 Study in Subjects with Elevated Cardiovascular Disease Risk
Monte Rosa Therapeutics (GLUE) will present MRT-8102 GFORCE-1 Phase 1 study results during a webcast on October 1, 2026.
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Rhea-AI Summary
Monte Rosa Therapeutics (GLUE) will present MRT-8102 GFORCE-1 Phase 1 study results during a webcast on October 1, 2026. The presentation begins at 8:00 a.m. ET and covers subjects with elevated cardiovascular disease risk. It will review safety and activity data across multiple dose levels following 4 weeks of treatment, including effects on drivers of atherosclerotic cardiovascular disease.
Details
Market move: GLUE +6.04% vs previous close. Phase 1 MRT-8102 clinical data
On Sep 30, the day this news came out, the latest delayed price for GLUE is 6.04% above the previous close. Our momentum scanner has recorded 7 alerts for this stock so far that day. The latest delayed price is $12.65.
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Key Figures
- Presentation time
- 8:00 a.m. ET on Oct. 1, 2026
- GFORCE-1 Phase 1 results presentation
- Treatment duration
- 4 weeks
- MRT-8102 safety and activity data across multiple dose levels
Previous Clinical trial Reports
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Interim MRT-8102 results reported hsCRP reductions and NEK7 degradation in elevated CVD-risk subjects.
24h Move is the share-price change in the day after each event; other market factors may also have contributed.
Key Terms
molecular glue degrader technical
atherosclerotic cardiovascular disease medical
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Conference call and webcast to be held at 8:00 a.m. ET on Oct. 1, 2026
BOSTON, Sept. 30, 2026 (GLOBE NEWSWIRE) -- Monte Rosa Therapeutics, Inc. (Nasdaq: GLUE), a clinical-stage biotechnology company developing novel molecular glue degrader (MGD)-based medicines, today announced that management will host a live conference call and webcast on Thursday, October 1, at 8:00 a.m. ET. The webcast presentation will review clinical results from the GFORCE-1 Phase 1 study of the NEK7-directed MGD MRT-8102 in subjects with elevated cardiovascular disease (CVD) risk. The presentation will include safety and activity data for MRT-8102 across multiple dose levels following 4 weeks of treatment and will showcase pioneering data on the modulation of multiple pathogenic drivers of atherosclerotic cardiovascular disease (ASCVD) by MRT-8102.
A webcast of the presentation will be accessible via the “Events & Presentations” section of Monte Rosa’s website at ir.monterosatx.com. Registration for the conference call is available at the following link. An archived version of the webcast will be made available for 30 days following the presentation.
About Monte Rosa
Monte Rosa Therapeutics is a clinical-stage biotechnology company developing highly selective molecular glue degrader (MGD) medicines for patients living with serious diseases. MGDs are small molecule protein degraders that have the potential to treat many diseases that other modalities, including other degraders, cannot. Monte Rosa’s QuEEN™ (Quantitative and Engineered Elimination of Neosubstrates) discovery engine combines AI-guided chemistry, diverse chemical libraries, structural biology, and proteomics to rationally design MGDs with unprecedented selectivity. Monte Rosa has developed the industry’s leading pipeline of first-in-class and only-in-class MGDs, spanning autoimmune and inflammatory diseases, oncology, and beyond, with three programs in the clinic. Monte Rosa has ongoing collaborations with leading pharmaceutical companies in the areas of immunology, oncology, and neurology. For more information, visit www.monterosatx.com.
Investors
Andrew Funderburk
ir@monterosatx.com
Media
Cory Tromblee, Scient PR
media@monterosatx.com