| Valuation method | Value, $ | Upside, % |
|---|---|---|
| Artificial intelligence (AI) | 41.98 | n/a |
| Intrinsic value (DCF) | 0.53 | n/a |
| Graham-Dodd Method | n/a | |
| Graham Formula | 167.26 | n/a |
Synlogic, Inc. (NASDAQ: SYBX) is a clinical-stage biopharmaceutical company pioneering the development of synthetic biotic medicines to address metabolic and immunological diseases. Headquartered in Cambridge, Massachusetts, Synlogic leverages synthetic biology to engineer beneficial microbes that function as living therapeutics. The company’s pipeline includes SYNB1618 and SYNB1934 (Phase II candidates for phenylketonuria), SYNB1353 (targeting homocystinuria), SYNB8802 (Phase I for enteric hyperoxaluria), and SYNB1891 (Phase I for solid tumors). Synlogic’s innovative approach focuses on non-systemic, orally administered treatments, offering potential advantages in safety and efficacy. Collaborations with Roche and Ginkgo Bioworks bolster its R&D capabilities. Operating in the high-growth biotechnology sector, Synlogic aims to transform disease treatment through engineered microbial therapies, positioning itself at the forefront of synthetic biology-driven drug development.
Synlogic presents a high-risk, high-reward investment opportunity due to its early-stage clinical pipeline and innovative synthetic biotic platform. The company’s focus on rare metabolic diseases and oncology addresses unmet medical needs with significant market potential. However, its financials reflect typical biotech challenges: minimal revenue ($8K in latest reporting), substantial net losses (-$23.4M), and negative operating cash flow (-$31.7M). With $18.9M in cash and no debt, liquidity appears limited relative to burn rates. The low beta (0.56) suggests lower volatility versus peers, but clinical trial failures or delays could severely impact valuation. Investors should weigh the transformative potential of its platform against the inherent risks of pre-commercial biotech investing.
Synlogic’s competitive advantage lies in its proprietary synthetic biotic platform, which engineers microbes to perform therapeutic functions locally (e.g., gut or tumor microenvironment), reducing systemic side effects. This differentiates it from traditional small-molecule or biologic approaches in metabolic diseases. However, the company faces intense competition from established rare-disease players like BioMarin (PKU market leader) and newer gene-editing therapies. In oncology, SYNB1891’s intratumoral delivery competes with checkpoint inhibitors and CAR-T therapies. Synlogic’s collaborations with Roche provide validation but also expose dependency risks. Its capital efficiency is a concern—competitors with deeper pipelines (e.g., CRISPR Therapeutics) may outpace development. The lack of near-term commercialization pathways and reliance on external partnerships weaken its positioning against vertically integrated peers. Success hinges on demonstrating clinical superiority in niche indications where synthetic biology offers clear mechanistic advantages.