Affini-T
Affini-T orchestrates the immune system to target oncogenic driver mutations to deliver transformative therapies intended to cure patients.
Affini-T orchestrates the immune system to target oncogenic driver mutations to deliver transformative therapies intended to cure patients.
Affini-T orchestrates the immune system to target oncogenic driver mutations to deliver transformative therapies intended to cure patients.
Developing novel therapies for patients with rare bone and connective tissue disorders.
Developing novel therapies for patients with rare bone and connective tissue disorders.
Developing a proprietary platform which leverages novel parvoviruses that have been pressure tested by nature to target specific tissues, carry a larger cargo, with minimal neutralizing immunity and the potential to re-dose.
Developing a proprietary platform which leverages novel parvoviruses that have been pressure tested by nature to target specific tissues, carry a larger cargo, with minimal neutralizing immunity and the potential to re-dose.
Developing first-in-class CAR-macrophage platform for oncology and non-oncology applications.
Developing first-in-class CAR-macrophage platform for oncology and non-oncology applications.
Developing treatments derived from proprietary discovery platform for CNS disorders and neurodegenerative diseases.
Developing treatments derived from proprietary discovery platform for CNS disorders and neurodegenerative diseases.
Cyrus solves difficult protein engineering and structure prediction problems using the most scientifically advanced, powerful, and laboratory-proven software.
Cyrus solves difficult protein engineering and structure prediction problems using the most scientifically advanced, powerful, and laboratory-proven software.
Developing innovative medicines in immunology. Went public in 2021 and was formerly NASDAQ:DICE.
Developing innovative medicines in immunology. Went public in 2021 and was formerly NASDAQ:DICE.
Harnessing the immune system for improved patient outcomes using a targeted approach.
Harnessing the immune system for improved patient outcomes using a targeted approach.
Overcoming the challenge of intracellular target access to transform the treatment of devastating diseases.
Overcoming the challenge of intracellular target access to transform the treatment of devastating diseases.
Drugging transcription factor complexes through novel pockets, or ‘switch sites’, for cancer.
Drugging transcription factor complexes through novel pockets, or ‘switch sites’, for cancer.
Minimal residual disease testing platform.
Pioneering the most comprehensive multiomics platform for early cancer detection.
Pioneering the most comprehensive multiomics platform for early cancer detection.
Broadly applicable biologics platform across many different therapeutic areas.
Broadly applicable biologics platform across many different therapeutic areas.
Exploring uncharted territories in immunomodulation comprising Butyrophilins & Gamma-delta T cells.
Exploring uncharted territories in immunomodulation comprising Butyrophilins & Gamma-delta T cells.
Developing targeted therapeutics for complex diseases using novel single cell analyses.
Developing targeted therapeutics for complex diseases using novel single cell analyses.
Gene therapy company developing a paradigm-shifting platform for in vivo cell-specific gene delivery.
Gene therapy company developing a paradigm-shifting platform for in vivo cell-specific gene delivery.
Preclinical stage biotechnology company developing antibody-based therapeutics to halt fibrosis in a variety of organ systems.
Preclinical stage biotechnology company developing antibody-based therapeutics to halt fibrosis in a variety of organ systems.
Discovering breakthrough gene editing systems for curing disease.
Discovering breakthrough gene editing systems for curing disease.
circRNA platform company for next-generation therapies and vaccines.
circRNA platform company for next-generation therapies and vaccines.
Developing therapeutics for rare cancers, including anaplastic astrocytoma.
Developing therapeutics for rare cancers, including anaplastic astrocytoma.
Developing gene therapies for rare immunology disorders. Went public in 2018 and was formerly NASDAQ:ORTX.
Developing gene therapies for rare immunology disorders. Went public in 2018 and was formerly NASDAQ:ORTX.
Developing therapeutics for rare dermatological disorders.
Developing therapeutics for rare dermatological disorders.
Targeting a range of fibrotic diseases, with a focus on fibrotic tissue-specific inhibition of integrins.
Targeting a range of fibrotic diseases, with a focus on fibrotic tissue-specific inhibition of integrins.
Gene-editing platform to overcome cancers, cure genetic diseases, and enable development of safer food.
Gene-editing platform to overcome cancers, cure genetic diseases, and enable development of safer food.
Synthetic biology and manufacturing company developing next-generation solutions for new therapeutics and vaccines.
Synthetic biology and manufacturing company developing next-generation solutions for new therapeutics and vaccines.
Charting a course to therapeutics for difficult-to-treat cancers.
Charting a course to therapeutics for difficult-to-treat cancers.
Developing targeted biotherapeutics that rebalance the immune system.
Developing targeted biotherapeutics that rebalance the immune system.
Small molecule platform company for alternative modulation of RNA.
Small molecule platform company for alternative modulation of RNA.
Innovation engine for novel antibody therapies
Innovation engine for novel antibody therapies
Applying an all-in-human, artificial intelligence powered drug discovery platform to unlock new drugs at scale.
Applying an all-in-human, artificial intelligence powered drug discovery platform to unlock new drugs at scale.
Overcoming current limitations of CAR-T cell therapeutics by using combining cell and gene editing technologies that address unmet patient need.
Overcoming current limitations of CAR-T cell therapeutics by using combining cell and gene editing technologies that address unmet patient need.
Bringing best-in-class immune-based therapies to patients in need.
Bringing best-in-class immune-based therapies to patients in need.