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DoriNano logo
Spring 2024

DoriNano

DoriNano aims to harness the potential of DNA origami technology to develop safe, effective, and low-cost combination nanomedicines that have precise cellular targeting with minimal effective doses of cargo for serious diseases. The company’s platform sets out to solve the past limitations of nanoparticles for delivering therapeutic cargo, offering unique advantages such as programmable size…

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Hestia Therapeutics logo
Spring 2024

Hestia Therapeutics

Hestia Therapeutics, lending its name from the Greek goddess of the hearth, aims to bring inflammatory cells into the tumor microenvironment to unleash anti-tumor effects from within. Currently, more than 70% of cancer patients have tumors that are shielded from the immune cells directed by checkpoint inhibitors to kill cancer cells, leading to disease progression.…

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Koi Biotherapeutics logo
Spring 2024

Koi Biotherapeutics

Koi Biotherapeutics is focused on solving a fundamental challenge in CAR T-cell therapy—the lack of long-term persistence of CAR T-cells post-infusion. Koi has developed a novel CAR-Enhancer protein that selectively targets CAR T-cells and promotes their development into memory cells, thereby enhancing their activity and in vivo persistence and eliminating the need for additional engineering…

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Nucyrna Therapeutics logo
Spring 2024

Nucyrna Therapeutics

Nucyrna Therapeutics aims to address the unmet medical needs in ALS and other CNS disorders through its next-gen RNA-targeting technology. Nucyrna’s oligonucleotide platform can target both Nuclear & Cytoplasmic RNA, enabling unique RNA-targeting capacities for addressing complex pathology. Demonstrating a remarkable therapeutic index profile in CNS, the company is focused on neurodegenerative diseases.

  • Joseph Klim, PhD

    Director of Neuroscience

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Sphinxion Therapeutics logo
Spring 2024

Sphinxion Therapeutics

Sphinxion Therapeutics leverages decades of academic research to bring forward therapeutic options targeting the sphingolipid metabolic pathway as a treatment for rare and common fibrotic diseases. Preliminary animal models in two specific diseases have been effectively treated with AAV gene therapy.

  • Julie Saba, MD, PhD

    The John & Edna Beck Chair in Pediatric Cancer Research, UCSF

  • Biren Shah, MBA

    Advisor, Revolution Medicines

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Cloverleaf Bio logo
Fall 2023

Cloverleaf Bio

Cloverleaf Bio has developed a new type of RNA therapeutics, based on tRNAs. Its engineered tRNAs have a broad range of applications including oncology, viral infection, and neurodegenerative disorders. Cloverleaf’s patented tRNAs target core components of the cellular translation machinery—tRNA modifying enzymes—that are essential for disease progression.

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Eascra Biotech logo
Fall 2023

Eascra Biotech

Eascra Biotech is an early-stage nanomedicine start-up launched in Nov 2021. Its proprietary therapeutic delivery platform can deliver RNA, gene editing, and other therapeutic options to hard-to-penetrate tissues such as cartilage, kidney, brain, and some solid tumors. Eascra is partnering with NASA to advance its science here on earth.

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Externa logo
Fall 2023

Externa

Externa is a platform technology company from the Church and Collins labs that combines synthetic biology, chemistry, and machine learning to bring the power of medicinal chemistry to protein therapeutics with synthetic amino acids. These new-to-nature amino acids give proteins new capabilities, such as irreversible binding, longer stability, or pH-dependent activity.

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PathCision Medicine, Inc logo
Fall 2023

PathCision Medicine, Inc

PathCision Medicine is harnessing tissue pathology insights to develop new targeted therapies. Built using a translational lens with a multi-omics approach, its proprietary discovery platform uncovers novel therapeutic avenues previously unavailable to patients with complex diseases. PathCision’s leading program is focused on developing a biologic modality for metastasis-selective delivery for multiple indications.

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Tezcat Biosciences, Inc logo
Fall 2023

Tezcat Biosciences, Inc

Tezcat Biosciences is developing a portfolio of protein-drug conjugates to provide therapeutic options for patients harboring mutant RAS cancers. Tezcat’s current portfolio consists of conjugates combining its proprietary protein carrier with established drug payloads. To-date, Tezcat’s drug development has been supported by academic collaborations and government awards.

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General Biologics, Inc logo
Spring 2023

General Biologics, Inc

General Biologics is a protein engineering company with a platform technology that targets therapeutic proteins to red blood cell precursors and mature red blood cells.  This enhances plasma half-life and shields therapeutic proteins from the immune system, and when needed, will activate red blood cell production without side effects.

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Ilios Therapeutics, Inc logo
Spring 2023

Ilios Therapeutics, Inc

Ilios Therapeutics utilizes a proprietary modular chemistry platform to develop first-in-class multi-valent small molecules modulating multiple complementary mechanisms involved in neurodegenerative diseases.

  • Dr. Fares Nigim

    Founder

  • Luca Giani

    Founder & CEO

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