| 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 |
Chemomab Therapeutics Ltd. (NASDAQ: CMMB) is a clinical-stage biotechnology company focused on developing innovative therapies for inflammation and fibrosis-related diseases. Headquartered in Tel Aviv, Israel, Chemomab's lead candidate, CM-101, is a humanized monoclonal antibody targeting soluble chemokine CCL24, a key driver in fibrotic and inflammatory conditions. The company is primarily advancing CM-101 for primary sclerosing cholangitis (PSC) and systemic sclerosis (SSc), two serious diseases with high unmet medical needs. With a strong scientific foundation and a pipeline centered on novel mechanisms, Chemomab aims to address significant gaps in fibrosis and inflammatory disease treatment. As a clinical-stage biotech, the company operates in a high-risk, high-reward sector, where successful drug development could lead to substantial market opportunities. Investors should note that Chemomab is pre-revenue, with its valuation tied to clinical progress and partnerships.
Chemomab Therapeutics presents a high-risk, high-reward investment opportunity typical of clinical-stage biotech firms. The company's lead candidate, CM-101, targets niche fibrotic and inflammatory diseases with limited treatment options, potentially offering significant upside if clinical trials succeed. However, with no revenue, negative earnings, and a market cap of just ~$1.3M, the company faces substantial financial and clinical development risks. Investors must weigh the promising science against the binary nature of biotech outcomes, dilution risk from future fundraising, and competition in the fibrosis space. The low beta (0.629) suggests relative insulation from broad market movements, but the stock remains highly speculative.
Chemomab's competitive positioning hinges on the uniqueness of its CCL24-targeting approach in fibrosis and inflammation. The company's focus on PSC and SSc allows it to carve out a niche in orphan disease markets with high unmet needs. CM-101's mechanism of action differentiates it from broader anti-fibrotic approaches, potentially offering better safety and efficacy profiles. However, Chemomab faces intense competition from larger biopharma companies developing fibrosis therapies, including those targeting TGF-β, IL-11, and other pathways. The company's small size and limited resources constrain its ability to independently advance multiple programs or compete in commercialization. Success will depend on demonstrating clear clinical differentiation, securing partnerships, or attracting acquisition interest. Chemomab's Israeli base provides cost advantages in R&D but may complicate U.S. market access without a strategic partner.