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Monte Rosa Q1 net loss $44.5M; cash $671M; multiple pipeline advances
Net loss of $44.5M vs net income of $46.9M in Q1 2025; collaboration revenue fell to $4.2M from $84.9M.
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Monte Rosa posts Q4 net loss $46.1M; cash runway into 2029; positive Phase 1 data for NEK7 degrader MRT-8102
Q4 net loss $46.1M vs $13.4M in Q4 2024; full-year net loss decreased to $38.6M from $72.7M.
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Monte Rosa prices $300M public offering of common stock and pre-funded warrants
Offering of 11,125,000 shares at $24.00/share and pre-funded warrants for 1,375,000 shares at $23.9999 each.
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Monte Rosa reports positive interim Phase 1 data for MRT-8102; hsCRP reduced 85% in 4 weeks
In subjects with elevated CVD risk, MRT-8102 reduced hsCRP by 85% after 4 weeks; 94% achieved hsCRP <2 mg/L (median baseline 6.3 mg/L).
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MRT-2359 + enzalutamide shows 100% PSA response in AR-mutant mCRPC; Phase 2 planned 2026
In 14 evaluable mCRPC patients, overall DCR 64% (9/14); in AR-mutant subset (n=4), 100% PSA response rate and 100% DCR, with 2 RECIST partial responses.
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Monte Rosa reports Q3 net loss $27.1M; second Novartis deal with $120M upfront
Net loss $27.1M vs $23.9M YoY; collaboration revenue $12.8M (vs $9.2M).
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Monte Rosa and Novartis expand collaboration for immune-disease degraders; upfront $120M
Monte Rosa receives $120M upfront from Novartis under new collaboration for degraders in immune-mediated diseases.
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Monte Rosa Q2 net loss narrows to $12.3M on $23.2M collaboration revenue; cash runway to 2028
Collaboration revenue $23.2M (vs $4.7M YoY) from Novartis license; net loss improved to $12.3M from $30.3M.
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Monte Rosa Q1 net income $46.9M on Novartis revenue; pipeline advances
Net income of $46.9M vs net loss of $32.0M a year ago; collaboration revenue $84.9M from Novartis.
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Monte Rosa Q4 net income $13.4M; Ph1 MRT-6160 >90% VAV1 deg, MRT-2359 CRPC response
Q4 2024 net income $13.4M vs net loss $33.3M in Q4 2023; collaboration revenue $60.6M from Novartis/Roche deals.
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Monte Rosa sets RP2D for MRT-2359 at 0.5 mg/day 21/7 schedule; safety, PD data positive
RP2D selected: 0.5 mg daily on 21-days-on/7-days-off schedule based on favorable safety and ~60% GSPT1 degradation.
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Monte Rosa reports Q3 net loss $23.9M; announces Novartis deal for VAV1 degraders with $150M upfront
Net loss of $23.9M for Q3 2024; collaboration revenue of $9.2M from Roche.
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Monte Rosa licenses VAV1 degrader MRT-6160 to Novartis for $150M upfront
Novartis gets exclusive worldwide rights to develop, manufacture, and commercialize VAV1 MGDs including MRT-6160.
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Monte Rosa Q2 net loss $30.3M; cash $267.1M; IND cleared for MRT-6160
Net loss $30.3M for Q2 2024 vs $32.0M in Q1; collaboration revenue $4.7M from Roche deal.
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Monte Rosa: MRT-2359 dose update; MRT-6160 IND for autoimmune diseases
MRT-2359 Phase 1/2: favorable safety at 0.5 mg 21/7 schedule; evaluating 0.75 mg cohort; RP2D and updated data expected H2 2024.
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Monte Rosa prices $100M public offering of common stock and pre-funded warrants
Priced 10.6M shares at $4.70/share and pre-funded warrants for 10.6M shares at $4.6999/warrant; gross proceeds $100M.
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Monte Rosa Q1 net loss $32M; pipeline advances with MRT-2359, MRT-6160, MRT-8102 milestones
Q1 2024 net loss $32.0M; cash $197.8M (down from $237.0M Dec 2023), sufficient into H1 2026.
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Monte Rosa CSO Owen Wallace departs May 17 to become CEO at UK biotech; remains adviser
Owen Wallace resigns as CSO effective May 17, 2024, to become CEO of a UK-based biotech company.
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Monte Rosa reports Q4 2023 net loss $33.3M; cash into H1 2026; key pipeline milestones on track
Net loss Q4 2023 $33.3M ($30.8M prior year); FY net loss $135.4M; cash $237M, runway into H1 2026.