Cellinfinity Bio


Developer of engineered cell-therapy technologies that apply directed-evolution and genetic engineering to reprogram immune cells in vivo and ex vivo for treatment of solid tumors. The organization advances preclinical candidates for both in vivo gene-delivery–based T cell reprogramming and autologous CAR-T therapies, and pursues IND-enabling development and collaborations.

Industries

Biotechnology
Health Care
Life Science
Medical
Biotechnology Research

Nr. of Employees

small (1-50)

Cellinfinity Bio

West Haven, Connecticut, United States


Products

In vivo CAR-T therapy candidate (preclinical)

A preclinical candidate that uses in vivo gene-delivery to generate tumor-targeting T cells in patients, incorporating novel target selection and genetic enhancements for solid tumors.

Autologous CAR-T therapy candidate (preclinical)

A preclinical autologous CAR-T candidate that incorporates novel antigen targeting and cellular enhancements intended for solid-tumor indications.

Supercharged In Vivo Cell Therapy™

A simplified in vivo CAR-T cell therapy platform that allows the patient's own body to produce the therapy without the need for complex manufacturing or lymphodepletion.


Services

Partnerships to access preclinical cell-therapy candidates and to support lead optimization and IND-enabling activities.

Expertise Areas

  • Directed evolution for cell therapy
  • In vivo gene delivery and in situ immune-cell engineering
  • CAR design and T cell engineering
  • Tumor-target antigen discovery
  • Show More (2)

Key Technologies

  • Directed-evolution platforms
  • AAV-mediated gene delivery
  • Transposon-based gene delivery (Sleeping Beauty)
  • mRNA-encoded transposase delivery
  • Show More (5)

News & Updates

Announcement of publication and exclusive licensing of a novel CAR-design technology.

Announcement of publication and exclusive licensing of a novel gene-delivery technology.

Announcement regarding publication and licensing of a technology for directed evolution of cells to improve adoptive cell therapy.

Recipient of the 2022 Future Innovator Prize as noted in press coverage.


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