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Latus Bio develops gene therapies, precisely targeting specific cells and tissues to fundamentally impact genetic diseases. The company employs an integrated adeno-associated virus (AAV) discovery process, leveraging novel capsid variants and computational models. This technical approach enhances therapeutic potency, specificity, and manufacturability, aiming to reduce immunogenicity, toxicity, and required doses.
Established around 2024, Latus Bio was founded by CEO P. Peter Ghoroghchian, M.D., Ph.D., and Scientific Advisory Board Chair Beverly Davidson, Ph.D., emerging from breakthrough technology in Philadelphia. Their founding insight recognized the delivery vehicle's critical role in gene therapy, driving efforts to overcome high AAV dose challenges that cause toxicity and complex manufacturing.
Latus Bio’s pipeline focuses on patients with monogenic diseases, including CLN2 Disease and Huntington's Disease. The company’s mission is to transform genetic disorder treatments by refining therapeutic delivery. Its long-term vision is to provide a new generation of curative, precise, and accessible gene medicines.
Latus Bio has raised $54.0M across 1 funding round.
Latus Bio has raised $54.0M in total across 1 funding round.
Latus Bio has raised $54.0M across 1 funding round. Most recently, it raised $54.0M Series A in May 2024.
| Date | Round | Lead Investors | Other Investors | Status |
|---|---|---|---|---|
| May 1, 2024 | $54M Series A | Francisco Gimenez, Kiersten Stead | 5AM Ventures, 8VC, Alta Partners, Dcvc (data Collective), Insight Partners, Radical Ventures, Jack Boren, BEN Franklin Technology Partners, Gaingels, Modi Ventures, CHO HO Sung, The Children | Announced |
Latus Bio has raised $54.0M in total across 1 funding round.
Latus Bio's investors include Francisco Gimenez, Kiersten Stead, 5AM Ventures, 8VC, Alta Partners, DCVC (Data Collective), Insight Partners, Radical Ventures, Jack Boren, Ben Franklin Technology Partners, Gaingels, Modi Ventures.
Latus Bio is a biotechnology company developing precision AAV gene‑therapy delivery technologies and product candidates focused on central nervous system (CNS) and related disorders, using massively parallel in‑vivo capsid discovery and AI/ML to produce highly potent, cell‑specific capsids intended to enable lower‑dose, safer clinical programs[3][2].
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