| Valuation method | Value, $ | Upside, % |
|---|---|---|
| Artificial intelligence (AI) | 36.71 | -62 |
| Intrinsic value (DCF) | n/a | |
| Graham-Dodd Method | n/a | |
| Graham Formula | n/a |
Revolution Medicines, Inc. (NASDAQ: RVMD) is a clinical-stage precision oncology company pioneering therapies targeting RAS-addicted cancers, one of the most prevalent and challenging oncogenic drivers. Headquartered in Redwood City, California, the company focuses on developing inhibitors for frontier targets like SHP2, SOS1, and RAS(ON) variants, including KRASG12C and KRASG12D. Its lead candidate, RMC-4630 (an SHP2 inhibitor), is in Phase 1/2 trials for solid tumors, while RMC-6236 (a pan-RAS inhibitor) and RMC-6291 (a mutant-selective KRASG12C inhibitor) represent next-generation approaches. Revolution Medicines collaborates with Sanofi on SHP2 inhibitors, enhancing its R&D capabilities. With no approved products yet, the company is a high-growth biotech play in the $200B+ oncology market, targeting unmet needs in cancers driven by RAS mutations, which account for ~30% of all human malignancies. Its innovative pipeline positions it as a key disruptor in precision oncology.
Revolution Medicines offers high-risk, high-reward exposure to the burgeoning RAS-inhibitor space, with a $7.4B market cap reflecting investor optimism. The company’s deep pipeline—particularly RMC-6236’s potential as a first-in-class pan-RAS inhibitor—could address significant unmet needs in NSCLC, colorectal, and pancreatic cancers. However, with $543M in cash and a $557M annual operating burn, near-term dilution risk is elevated. Clinical catalysts in 2024 (RMC-6236 Phase 1/2 data) may drive volatility. The lack of revenue and reliance on binary trial outcomes make RVMD suitable only for risk-tolerant investors. Collaboration with Sanofi mitigates some development risk, but competition in KRASG12C (e.g., Amgen’s Lumakras) is intensifying.
Revolution Medicines’ competitive edge lies in its differentiated RAS(ON) inhibitor platform, which targets both mutant and wild-type RAS proteins—a key limitation of current KRASG12C inhibitors like Lumakras. While Amgen and Mirati focus on KRASG12C(OFF) inhibitors, RVMD’s RMC-6236 aims to inhibit multiple RAS variants in their active state, potentially overcoming resistance mechanisms. The company’s SOS1 (RMC-5845) and SHP2 (RMC-4630) inhibitors provide complementary mechanisms to block RAS pathway signaling. However, RVMD trails in commercialization experience versus Amgen or Bristol-Myers Squibb. Its collaboration with Sanofi provides validation but also exposes it to partnership dependencies. The pan-RAS approach is scientifically compelling but carries higher development risk versus target-specific therapies. RVMD’s IP portfolio around RAS(ON) chemistry could create barriers to entry, though Big Pharma’s interest in RAS (e.g., Pfizer’s KRAS programs) ensures fierce competition.