| Valuation method | Value, $ | Upside, % |
|---|---|---|
| Artificial intelligence (AI) | n/a | n/a |
| Intrinsic value (DCF) | 4.80 | -89 |
| Graham-Dodd Method | n/a | |
| Graham Formula | n/a |
Maze Therapeutics, Inc. (NASDAQ: MAZE) is a clinical-stage biopharmaceutical company pioneering small molecule precision medicines for renal, cardiovascular, metabolic diseases, and obesity. Headquartered in South San Francisco, California, Maze leverages genetic insights to develop targeted therapies, with its lead candidate, MZE829, in Phase II trials for APOL1-mediated kidney disease—a condition with high unmet need. The company’s second program, MZE782, targets SLC6A19 for chronic kidney disease (CKD) and is in Phase I. Founded in 2017, Maze combines functional genomics and drug discovery to address genetically defined patient populations, positioning itself in the high-growth precision medicine segment of the $1.3T global biopharma market. With a focus on underserved diseases, Maze aims to deliver transformative therapies while capitalizing on the rising demand for metabolic and renal treatments driven by aging populations and increasing obesity rates.
Maze Therapeutics presents a high-risk, high-reward opportunity for investors focused on precision medicine. The company’s lead candidate, MZE829, targets APOL1-mediated kidney disease—a niche with no approved therapies and a potential market exceeding $3B. Positive Phase II data could catalyze significant upside, but clinical-stage volatility remains a key risk. Maze’s $450M market cap reflects its early-stage pipeline, with revenue primarily from collaborations ($167.5M in 2024). A strong cash position ($196.8M) and modest debt ($26.6M) provide runway, but dilution risk persists given negative beta (-1.88) and reliance on trial outcomes. The obesity/metabolic focus aligns with sector trends, but competition from larger players like Novo Nordisk requires differentiation.
Maze Therapeutics competes in the crowded metabolic and renal disease space by focusing on genetically validated targets. Its key advantage lies in its precision medicine approach, targeting APOL1 and SLC6A19—mechanisms underserved by current therapies. Unlike broad-acting GLP-1 agonists (e.g., semaglutide), Maze’s candidates aim for genetically defined subsets, potentially reducing side effects and improving efficacy. However, the company faces scalability challenges versus giants like Novo Nordisk, which dominate obesity/CKD with established commercial infrastructure. Maze’s asset MZE829 could fill a critical gap in APOL1-mediated kidney disease, where Vertex (VRTX) is also active but with a different modality (gene editing). Pipeline depth is a weakness—only two clinical candidates—compared to peers like Regeneron (REGN) with diversified portfolios. Partnerships (e.g., with Roche) may offset resource constraints but could dilute ownership. Maze’s success hinges on Phase II data differentiation and securing niche indications before larger players enter.