
Monte Rosa Therapeutics
Developing next-generation small molecule protein degraders to treat cancer and beyond.
Date | Investors | Amount | Round |
---|---|---|---|
- | investor investor investor investor | €0.0 | round |
investor | €0.0 | round | |
investor investor | €0.0 | round | |
investor investor investor investor investor investor investor investor | €0.0 | round | |
investor investor investor investor investor investor investor investor investor investor investor investor investor | €0.0 Valuation: €0.0 -6.6x EV/EBITDA | round | |
N/A | €0.0 Valuation: €0.0 -12.4x EV/EBITDA | round | |
N/A | €0.0 | round | |
* | N/A | $100m | Post IPO Equity |
Total Funding | 000k |


















USD | 2020 | 2021 | 2022 | 2023 | 2024 | 2025 | 2026 |
---|---|---|---|---|---|---|---|
Revenues | 0000 | 0000 | 0000 | 0000 | 0000 | 0000 | 0000 |
% growth | - | - | - | - | - | 80 % | (61 %) |
EBITDA | 0000 | 0000 | 0000 | 0000 | 0000 | 0000 | 0000 |
% EBITDA margin | - | - | - | - | (97 %) | - | - |
Profit | 0000 | 0000 | 0000 | 0000 | 0000 | 0000 | 0000 |
% profit margin | - | - | - | - | (96 %) | - | - |
EV | 0000 | 0000 | 0000 | 0000 | 0000 | 0000 | 0000 |
EV / revenue | 00.0x | 00.0x | 00.0x | 00.0x | 00.0x | 00.0x | 00.0x |
EV / EBITDA | 00.0x | 00.0x | 00.0x | 00.0x | 00.0x | 00.0x | 00.0x |
R&D budget | 0000 | 0000 | 0000 | 0000 | 0000 | 0000 | 0000 |
R&D % of revenue | - | - | - | - | 161 % | - | - |
Source: Company filings or news article, Equity research estimates
Related Content
Monte Rosa Therapeutics is a clinical-stage biotechnology company that concentrates on creating a novel class of medicines known as molecular glue degraders (MGDs). Established in 2018 in Basel, Switzerland, and now headquartered in Boston, Massachusetts, the company was launched from the founding investor Versant Ventures' Ridgeline Discovery Engine. The company's leadership includes CEO Markus Warmuth, an M.D. with over two decades of experience in drug discovery and precision medicine, who previously held roles at Third Rock Ventures, H3 Biomedicine, and Novartis. His background in understanding the molecular mechanisms of diseases and developing targeted therapies is central to the company's direction.
The core of Monte Rosa's strategy is its proprietary QuEEN™ (Quantitative and Engineered Elimination of Neosubstrates) discovery engine. This platform integrates AI-guided chemistry, proteomics, structural biology, and diverse chemical libraries to rationally design MGDs. Unlike traditional drugs that inhibit protein function, MGDs act as small molecules that induce the proximity between a target disease-causing protein and an E3 ubiquitin ligase. This "gluing" action tags the unwanted protein for destruction by the cell's natural disposal system, the proteasome, effectively eliminating it. This mechanism allows the company to pursue therapeutic targets previously considered "undruggable" due to the lack of conventional binding sites.
The company's business model is centered on the discovery, development, and commercialization of its MGD pipeline candidates. Revenue generation is anticipated from the successful marketing of its own drugs and through strategic collaborations with larger pharmaceutical companies. Monte Rosa has entered into significant partnerships, including a global licensing agreement with Novartis to advance VAV1-directed MGDs for immune-related conditions and a collaboration with Roche to discover and develop MGDs for targets in oncology and neurological diseases. These partnerships provide non-dilutive funding, including substantial upfront payments and potential future milestone payments and royalties, which support the company's extensive R&D activities. The company secured initial funding through a Series A round of $32.5 million and a Series B of $96 million, before going public on the Nasdaq under the ticker 'GLUE' in June 2021, raising approximately $222.3 million.
Monte Rosa's therapeutic pipeline spans multiple disease areas, primarily oncology and autoimmune and inflammatory diseases. Key clinical-stage programs include MRT-2359 for MYC-driven solid tumors, MRT-6160 (licensed to Novartis) for autoimmune diseases, and MRT-8102 targeting NEK7 for inflammatory conditions. The company serves patients with serious diseases who may have limited or no effective treatment options, aiming to provide highly selective therapies that offer a new approach to treatment.
Keywords: molecular glue degraders, targeted protein degradation, QuEEN platform, drug discovery, clinical-stage biotechnology, oncology therapeutics, autoimmune disease treatment, inflammatory disease therapy, undruggable targets, Markus Warmuth, Versant Ventures, proteasome system, E3 ligase, protein elimination, Novartis collaboration, Roche collaboration, GLUE ticker, MRT-2359, MRT-6160, VAV1 degrader, NEK7 degrader, precision medicine, AI in drug discovery, proteomics, small molecule drugs