Ono Venture Investment

Ono Venture Investment, established in 2020, serves as the corporate venture capital arm of Ono Pharmaceutical Company. Based in San Carlos, California, the firm focuses on investing in healthcare and pharmaceutical companies, with a particular emphasis on oncology, immunology, and neurology. Ono Venture Investment aims to support the development of innovative solutions in these sectors, building on Ono Pharmaceutical's commitment to delivering groundbreaking medicines.

Shunichiro Matsumoto

Executive Vice President

Hiroshi Yamamoto

President and CEO

Shunichiro Matsumoto

CEO

12 past transactions

Harness Therapeutics

Venture Round in 2025
Harness Therapeutics is a private biotechnology company dedicated to developing a novel class of therapeutic RNAs known as SINEUPs®. This innovative technology allows for the precise upregulation of protein expression, providing a unique mechanism of action for challenging diseases. By significantly expanding the druggable proteome, Harness Therapeutics aims to address conditions that have been difficult to treat with traditional small molecules, biologics, or gene therapies. The company's primary focus is on central nervous system and ophthalmologic disorders, although the potential applications of its platform extend across various therapeutic areas. Harness Therapeutics is committed to meeting unmet medical needs by creating differentiated products that enhance the translation of important, validated neurodegenerative targets.

AIRNA

Series A in 2024
AIRNA is a biotechnology company specializing in the development of RNA editing therapies. Its platform enables the creation of therapeutics designed to treat both rare and common diseases, with the goal of improving patients' health.

Mozart Therapeutics

Series A in 2023
Mozart Therapeutics is a biotechnology startup dedicated to developing innovative therapies for autoimmune and inflammatory diseases. The company specializes in creating disease-modifying CD8 T cell modulators, leveraging a unique regulatory CD8 T cell network to target a specific subset of T lymphocytes. These modulators aim to restore immune balance and mitigate the damage caused by autoreactive and pathogenic immune responses. By focusing on first-in-class CD8 Treg modulators, Mozart Therapeutics seeks to delay the onset and improve the management of various autoimmune disorders, thereby providing healthcare professionals with advanced treatment options for their patients.

Violet Therapeutics

Venture Round in 2023
Violet Therapeutics is a pre-clinical stage biotechnology company focused on drug discovery for central nervous system diseases. The company utilizes innovative platforms that identify, map, and analyze cellular connectomes through barcoded viral tracing, offering insights into cell-cell interactions at a single-cell level. This approach aims to facilitate advancements in the understanding and treatment of neuroinflammation. Co-founded by Mass General Brigham Ventures and researchers from Brigham & Women’s Hospital, Violet Therapeutics is committed to exploring novel therapeutic targets to develop effective treatments for complex neurological conditions.

Curreio

Series A in 2023
Curreio is a biotechnology company focused on drug discovery through advanced structural analysis techniques. Utilizing cryo-electron microscopy, Curreio's platform enables researchers to observe in-vivo structures in a frozen state without the need for staining. This innovative approach facilitates the discovery and analysis of life-saving drugs, positioning Curreio at the forefront of structural analysis-based drug development methods. By providing cutting-edge technology, the company aims to enhance the efficiency and effectiveness of drug discovery processes.

Mediar Therapeutics

Series A in 2023
Mediar Therapeutics is a biotechnology company based in Cambridge, Massachusetts, founded in 2019. It specializes in developing antibody-based therapeutics targeting key fibrotic mediator proteins involved in fibrosis, aiming to halt and potentially reverse this condition in chronically damaged organs. The company operates at the pre-clinical stage.

Switch Therapeutics

Series A in 2023
Switch Therapeutics is a biotechnology company founded in 2020 and based in San Francisco, California. The company focuses on revolutionizing RNA interference (RNAi) therapies by developing biomarker-gated genetic medicines. These innovative therapies utilize nucleic acid nanotechnology and RNAi science to target a variety of diseases, particularly those affecting the central nervous system and other systemic conditions with significant unmet medical needs. Switch Therapeutics aims to provide healthcare providers with RNA molecules and therapies that can be activated selectively in specific cells, enhancing the precision of treatments for central nervous system diseases.

Casma Therapeutics

Series C in 2022
Casma Therapeutics, Inc. is a biotechnology company based in Cambridge, Massachusetts, that specializes in developing innovative therapeutic strategies centered on the natural cellular process of autophagy. Founded in 2017, the company aims to enhance autophagy to improve the clearance of unwanted proteins, organelles, and pathogens, thereby addressing significant medical challenges. Casma Therapeutics is advancing preclinical programs targeting various conditions, including muscle disorders, liver disease, inflammatory disorders, and neurodegenerative diseases. By harnessing and manipulating the autophagy system, the company seeks to arrest or reverse disease progression, ultimately enabling physicians to meet unmet medical needs and provide effective treatments for patients with serious health issues.

Photys Therapeutics

Series A in 2022
Photys Therapeutics is a biopharmaceutical company focused on developing bifunctional small molecules that provide precise control over protein post-translational modifications. This innovative platform allows for the restoration of protein function, repair of cellular signaling pathways, and enhancement of the body's natural disease-fighting abilities. Co-founded by prominent chemist Amit Choudhary from the Broad Institute and the Longwood Fund, Photys is supported by a scientific advisory board that includes renowned experts from institutions such as MIT, Salk Institute, and Berkeley. The company's unique approach aims to advance therapeutic options in the healthcare industry, particularly by targeting kinases and potentially phosphatases, to address various diseases effectively.

Immunitas Therapeutics

Series B in 2021
Immunitas Therapeutics, Inc. is a biotechnology company based in Cambridge, Massachusetts, focused on developing targeted therapeutics for patients with complex cancers. Founded in 2019, the company utilizes a single-cell sequencing platform to analyze the biology of immune cells within human tumors. This innovative approach allows Immunitas to identify novel drug targets and develop key biomarkers that guide patient selection for their therapies. By emphasizing research rooted in human biology, Immunitas aims to bridge the gap between laboratory discoveries and clinical applications. The company is advancing multiple programs toward early human studies, leveraging its expertise in antibody discovery and engineering to create effective treatments that modulate identified targets.

Curreio

Venture Round in 2021
Curreio is a biotechnology company focused on drug discovery through advanced structural analysis techniques. Utilizing cryo-electron microscopy, Curreio's platform enables researchers to observe in-vivo structures in a frozen state without the need for staining. This innovative approach facilitates the discovery and analysis of life-saving drugs, positioning Curreio at the forefront of structural analysis-based drug development methods. By providing cutting-edge technology, the company aims to enhance the efficiency and effectiveness of drug discovery processes.

Mediar Therapeutics

Seed Round in 2021
Mediar Therapeutics is a biotechnology company based in Cambridge, Massachusetts, founded in 2019. It specializes in developing antibody-based therapeutics targeting key fibrotic mediator proteins involved in fibrosis, aiming to halt and potentially reverse this condition in chronically damaged organs. The company operates at the pre-clinical stage.
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