| Valuation method | Value, $ | Upside, % |
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| Artificial intelligence (AI) | n/a | n/a |
| Intrinsic value (DCF) | n/a | |
| Graham-Dodd Method | n/a | |
| Graham Formula | n/a |
Alumis Inc. (NASDAQ: ALMS) is a clinical-stage biopharmaceutical company pioneering innovative therapies for autoimmune and neuroinflammatory disorders. Headquartered in South San Francisco, California, Alumis focuses on developing precision medicines targeting tyrosine kinase 2 (TYK2), a key regulator in immune signaling pathways. The company’s lead candidate, ESK-001, is an allosteric TYK2 inhibitor in development for plaque psoriasis, systemic lupus erythematosus (SLE), and non-infectious uveitis. Additionally, Alumis is advancing A-005, a CNS-penetrant TYK2 inhibitor for neuroinflammatory and neurodegenerative diseases. Operating in the high-growth biotechnology sector, Alumis aims to address significant unmet medical needs in autoimmune diseases, a market projected to exceed $150 billion by 2027. With a strong scientific foundation and a pipeline targeting validated pathways, Alumis is positioned as an emerging player in next-generation immunology therapeutics.
Alumis presents a high-risk, high-reward investment opportunity in the autoimmune therapeutics space. The company’s clinical-stage pipeline, particularly ESK-001, targets large indications with significant unmet needs, including plaque psoriasis and SLE. However, as a pre-revenue biotech, Alumis carries substantial clinical and regulatory risks, evidenced by its $294 million net loss in FY2023. The negative beta (-2.17) suggests potential non-correlation with broader markets, which may appeal to specialized healthcare investors. With $169.5 million in cash and equivalents, the company appears funded for near-term operations, but additional capital raises are likely required to advance its pipeline. Success in upcoming clinical readouts could drive substantial upside, while setbacks may pressure the stock given the competitive TYK2 inhibitor landscape.
Alumis competes in the crowded TYK2 inhibitor space, where differentiation hinges on selectivity, efficacy, and safety profiles. The company’s allosteric approach to TYK2 inhibition (ESK-001) theoretically offers advantages over competitors’ active-site binders, potentially enabling better safety by preserving JAK1-3 function. However, it faces formidable competition from Bristol-Myers Squibb’s Sotyktu (deucravacitinib), the first FDA-approved TYK2 inhibitor for psoriasis, which achieved $241 million in 2023 sales. Alumis must demonstrate superior efficacy or tolerability to displace this entrenched competitor. In neuroinflammation (A-005), Alumis’ CNS-penetrant strategy is distinctive but unproven clinically. The company’s modest $265 million market cap reflects its early-stage status versus larger peers. Key competitive risks include pipeline concentration (two TYK2 assets) and reliance on a single mechanism in markets where combination therapies dominate. Success will require clear differentiation in mid-stage trials and strategic partnerships to fund late-stage development.