Epicrispr Biotechnologies is a pioneering therapeutics company dedicated to developing advanced genetic medicines. The organization focuses on scientific research, platforms, and clinical pipelines to treat serious diseases.
Subscribe to see Epicrispr Biotechnologies’s full profile → the full roster, investors in every round, weekly hiring history and every corporate event
Epicrispr Biotechnologies is a biotechnology company headquartered in United States. It has raised at least $334.8M across the 3 funding rounds on record. Its most recent funding round, Series C, raised $90M in August 2026. Xcout tracks 8 named people at Epicrispr Biotechnologies, including Amber Salzman (Chief Executive Officer).
2 more named people on record for Epicrispr Biotechnologies, with roles, board committees and tenure — see the full roster →
At least $334.8M raised across the 3 rounds on record. Every round on record:
| Date | Round | Amount | Investors |
|---|---|---|---|
| Series C | $90M | 10 named | |
| Series C | $68M | 10 named | |
| SEC Form D filing | $176.8M | — |
Who invested in each round, lead investors, valuations and the co-investor graph — open the full funding history →
A few of Epicrispr Biotechnologies's closest competitors — see the full list of competitors and alternatives →
CRISPR Therapeutics AG (CRSP) is a biotechnology firm dedicated to pioneering gene-based medicines for severe diseases. The company achieves this through its exclusive Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) technology, which enables precise and targeted alterations to an organism's genetic code. Its extensive pipeline includes therapeutic candidates spanning multiple medical areas, such as blood disorders (hemoglobinopathies), various cancers (oncology), regenerative medicine, and rare conditions. The company's flagship investigational therapy is CTX001, an ex vivo CRISPR gene-edited treatment. This therapy aims to benefit patients with transfusion-dependent beta-thalassemia or severe sickle cell disease by modifying their own hematopoietic stem cells to markedly boost the production of fetal hemoglobin within red blood cells. CRISPR Therapeutics is also advancing several other genetically engineered allogeneic (donor-sourced) CAR-T investigational therapies: CTX110, designed to combat cluster of differentiation 19-positive malignancies; CTX120, which targets B-cell maturation antigen for multiple myeloma that has relapsed or proven resistant to previous treatments; and CTX130, focused on Cluster of Differentiation 70 for a spectrum of solid tumors and blood cancers. Furthermore, the company is developing VCTX210, an immune-evasive, gene-edited stem cell-derived product candidate for treating type 1 diabetes. It is also pursuing various in vivo gene-editing initiatives aimed at addressing disorders affecting the liver, lungs, muscles, and central nervous system. The company has forged strategic alliances with significant partners, including Bayer Healthcare LLC, Vertex Pharmaceuticals Incorporated, ViaCyte, Inc., Nkarta, Inc., and Capsida Biotherapeutics. CRISPR Therapeutics AG was established in 2013 and maintains its headquarters in Zug, Switzerland.
EVOPOINT BIOSCIENCES CO., LTD. is an innovation-driven pharmaceutical company that focuses on precision oncology, multi-drug resistant bacterial infections, and metabolic diseases. Utilizing core platforms such as small molecule targeted drug development, complex antibody drug development, and targeted protein degradation, the company researches and develops innovative drug pipelines to provide treatment solutions for patients globally.
SNIPR Biome is a clinical-stage life sciences company headquartered in Copenhagen, Denmark, pioneering precision medicines and CRISPR-guided technologies for difficult-to-treat conditions.
Base Therapeutics is a biotechnology company that develops next-generation gene editing technologies, including its proprietary AccuBase base editing system and enhanced prime editing technology. The company focuses on creating therapeutic solutions for cancer and genetic diseases, alongside engineered immune cell therapies such as BASE-NK and CAR-T products. It serves patients and partners with pharmaceutical and agricultural enterprises by licensing its precision gene editing tools.
Arbor Biotechnologies, Inc. is a next-generation gene editing company focused on discovering and developing precise genetic medicines for rare and complex diseases.
YolTech Therapeutics is a clinical-stage biotechnology company that specializes in developing in vivo gene editing therapies and mRNA drugs for serious diseases. The company utilizes novel CRISPR-Cas enzymes, base editors, and lipid nanoparticle delivery systems to create precision genetic medicines.
Funding rounds, acquisitions, new executives, launches and expansions, each with a two-line summary and a link to the source. One short email a day, only when there is news.
Free: up to 5 companies, daily. Subscribers also follow whole sectors and saved filters (M&A in Israel, AI funding…), get instant alerts, in-app notifications and signed webhooks, and open the full profile behind every name. Subscribe →
Post the link and the card appears automatically — each network fetches the image itself.