| Valuation method | Value, $ | Upside, % |
|---|---|---|
| Artificial intelligence (AI) | n/a | n/a |
| Intrinsic value (DCF) | n/a | |
| Graham-Dodd Method | n/a | |
| Graham Formula | n/a |
Artelo Biosciences, Inc. (NASDAQ: ARTL) is a clinical-stage biopharmaceutical company pioneering treatments targeting the endocannabinoid system to address unmet medical needs in oncology, inflammatory diseases, and mental health. The company’s pipeline includes ART27.13, a synthetic G protein-coupled receptor agonist in Phase 1b/2a trials for cancer-related anorexia; ART12.11, a cannabidiol cocrystal for inflammatory bowel disease and PTSD; and ART26.12, a fatty acid binding protein 5 inhibitor for prostate/breast cancer and PTSD. Headquartered in Solana Beach, California, Artelo leverages collaborations like its partnership with Trinity College Dublin to advance its cachexia-focused research. Operating in the high-growth biotechnology sector, Artelo aims to capitalize on the expanding market for cannabinoid-based therapeutics, projected to exceed $50 billion by 2030. With no commercial revenue yet, the company’s value hinges on clinical milestones and strategic partnerships.
Artelo Biosciences presents a high-risk, high-reward opportunity for investors comfortable with early-stage biotech volatility. The company’s focus on the endocannabinoid system taps into a rapidly growing therapeutic area, but its $3.1M market cap reflects significant clinical and funding risks. With $6.9M in cash (as of FY2022) and an annual burn rate of ~$8M, near-term dilution risk is elevated. Key catalysts include Phase 1b/2a data for ART27.13 in cancer anorexia—a $2B+ potential market with limited competition. However, the lack of revenue, negative EPS (-$3.49), and preclinical status of other candidates necessitate cautious evaluation. Investors should monitor clinical progress and partnership developments closely.
Artelo competes in the niche but increasingly crowded endocannabinoid therapeutics space, differentiating itself through a diversified pipeline targeting both oncology and CNS disorders. Its lead asset ART27.13’s focus on cancer cachexia/anorexia provides first-mover potential in a space dominated by palliative care options like megestrol acetate. The cocrystal technology behind ART12.11 could offer bioavailability advantages over pure CBD formulations, though it faces stiff competition from Epidiolex in IBD. Artelo’s academic collaboration with Trinity College Dublin provides research credibility but lacks the commercialization firepower of larger peers’ partnerships. Financially, the company’s micro-cap status limits R&D scalability versus deep-pocketed competitors, necessitating selective pipeline prioritization. Its FABP5 inhibitor program (ART26.12) is scientifically distinctive but trails more advanced oncology candidates in the market. Success hinges on demonstrating clinical differentiation in targeted indications where Big Pharma presence remains limited.