![]() Sangamo Therapeutics France Sangamo Therapeutics France (formerly known as TxCell) is a biotechnology company that develops platforms for innovative, personalized T cell immunotherapies for the treatment of severe inflammatory and autoimmune diseases with high unmet medical needs. | ![]() Karius Karius is a life sciences company focused on conquering infectious diseases through the innovative use of next-generation sequencing to analyze microbial cell-free DNA. | ![]() Dicerna Pharmaceuticals Dicerna Pharmaceuticals is a clinical-stage biopharmaceutical company that focuses on the discovery and development of treatments for rare inherited diseases. | ||
Founding Date | Founding Date 2001 | Founding Date 2014 | Founding Date 2015 | Founding Date 2007 |
Type | Type Subsidiary | Type Private | Type Private | Type Subsidiary |
Tags | ||||
Locations | Locations Valbonne, FR HQ | Locations Redwood City, US HQ | Locations Cambridge, US HQ | Locations Cambridge, US HQ Boulder, US Lexington, US |
Employees | Employees 7 | Employees 205 | Employees 1332% increase | Employees 1042% decrease |
Financial | ||||
Revenue (est.) | Revenue (est.) €2.2m (FY, 2017) | Revenue (est.) N/A | Revenue (est.) N/A | Revenue (est.) $164.3m (FY, 2020) |
Net income | Net income (€10.9m) (FY, 2017) | Net income N/A | Net income N/A | Net income ($112.7m) (FY, 2020) |
Funding | ||||
Latest funding round | Latest funding round N/A | Latest funding round $ 165m (over 6 years ago) | Latest funding round $ 125m (over 5 years ago) | Latest funding round N/A |
Total funding raised | Total funding raised $ 71.6m | Total funding raised $ 220m | Total funding raised $ 265m | Total funding raised $ 287.1m |

Karius is a life sciences company focused on conquering infectious diseases through the innovative use of next-generation sequencing to analyze microbial cell-free DNA.
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eGenesis is a biotechnology company that develops human-compatible (HuCo) organs and cells.
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Dicerna Pharmaceuticals is a clinical-stage biopharmaceutical company that focuses on the discovery and development of treatments for rare inherited diseases.
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