Monte Rosa Therapeutics, Inc.
NASDAQ•GLUE
CEO: Dr. Markus Warmuth M.D.
Sector: Healthcare
Industry: Biotechnology
Listing Date: 2021-06-24
Monte Rosa Therapeutics, Inc., a clinical-stage biotechnology company, engages in the development of novel small molecule precision medicines that employ the body's natural mechanisms to selectively degrade therapeutically relevant proteins. The company develops MRT-2359, an orally bioavailable molecular glue degrader targeting the translation termination factor protein GSPT1 for the treatment of MYC-driven tumors; MRT-6160 for the treatment of systemic and central nervous system autoimmune diseases; and MRT-8102 for the treatment of IL-1?/NLRP3 driven inflammatory diseases. It also develops CDK2 to treat ovarian, uterine, and breast cancers. The company was incorporated in 2019 and is headquartered in Boston, Massachusetts.
Contact Information
Market Cap
$978.80M
P/E (TTM)
-25.5
17.3
Dividend Yield
--
52W High
$25.77
52W Low
$3.50
52W Range
Rank61Top 91.5%
2.0
F-Score
Modified Piotroski Analysis
Based on 6-year fundamentals
Weak • 2 / 9 points
Scoring Range (0-9)
8-9: Excellent Value
6-7: Strong Fundamentals
4-5: Average Quality
0-3: Weak Performance
Data Period: 2020-2025
Financial Dashboard
Q4 2025 Data
Revenue
$2.78M+0.00%
4-Quarter Trend
EPS
-$0.70+0.00%
4-Quarter Trend
FCF
-$43.78M+0.00%
4-Quarter Trend
2025 Annual Earnings Highlights
Key Highlights
Collaboration Revenue Growth Collaboration revenue reached $123.7 M in 2025, up $48.0 M from $75.6 M in 2024, driven by Roche and Novartis agreements.
Net Loss Significantly Narrowed Net loss narrowed to $(38.6) M in 2025, significantly down from $(72.7) M loss reported for the fiscal year ended 2024.
Major Financing Secured Completed 2026 Offering, raising net proceeds of $323.8 M to fund operations and capital requirements into 2029.
MRT-6160 Phase 1 Success Phase 1 results showed deep VAV1 degradation (>90%) and functional inhibition in peripheral blood T and B cells following dosing.
Risk Factors
Need Substantial Future Funding Requires substantial additional funding beyond current capital to complete development, scale operations, and achieve commercialization.
Limited Operating History Risks Biotech company with limited history; never generated revenue from drug sales; anticipates continued operating losses for foreseeable future.
Pipeline Execution Uncertainty Success depends on timely clinical trial completion and regulatory approval for lead candidates like MRT-2359 and MRT-8102.
IP Protection and Enforcement Patent portfolio subject to challenges; enforceability uncertain; competitors could develop similar technology, impairing competitive position.
Outlook
Advance MRT-8102 ASCVD Study Plan to initiate GFORCE-2 Phase 2 study for MRT-8102 in ASCVD patients defined by Stage 3/4 CKD and elevated CRP in H2 2026.
Advance MRT-2359 Oncology Study Plan Phase 2 study for MRT-2359 combination therapy in heavily pretreated mCRPC patients with AR mutations, anticipated start in 2026.
Submit Cyclin E1 IND Expect to submit IND application for cyclin E1-directed MGD molecule during 2026 calendar year to advance cell cycle program.
Expand Discovery Engine Capabilities Continue enhancing QuEENTM engine to target undruggable proteins and leverage additional E3 ligase systems beyond cereblon.
Peer Comparison
Revenue (TTM)
$262.60M
$244.06M
$197.09M
Gross Margin (Latest Quarter)
672.1%
124.4%
100.0%
Key Metrics
Symbol | Market Cap | P/E (TTM) | ROE (TTM) | Debt to Assets |
|---|---|---|---|---|
| ERAS | $4.45B | -32.6 | -34.5% | 11.9% |
| DAWN | $2.21B | -20.6 | -23.4% | 0.5% |
| VIR | $1.41B | -2.8 | -49.3% | 18.6% |
Long-Term Trends
Last 4 Quarters
Revenue
Net Income
Operating Cash Flow
4Q Revenue CAGR
-68.0%
Growth Under Pressure
4Q Net Income CAGR
N/M
Profitability Shift
Cash Flow Stability
25%
Cash Flow Needs Attention
Deep Research
Next earnings:May 6, 2026
EPS:-
|Revenue:-
Financials
Earnings Calls
Reports
News
Income Statement
Balance Sheet
Cash Flow Statement
Ratios
% Chg.
Income Statement | LTM |
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