Bristol-Myers Squibb

Bristol-Myers Squibb is a global biopharmaceutical company that discovers, develops, manufactures, and markets medicines across hematology, oncology, cardiovascular, and immunology. Its portfolio includes Opdivo for cancer immunotherapy; Eliquis for stroke prevention and venous thromboembolism; Orencia for rheumatoid arthritis; Sprycel, Yervoy, Empliciti, Baraclude; Reyataz and Sustiva for HIV; and Daklinza, Sunvepra, Beclabuvir for viral infections. The company sells products through wholesalers, retail pharmacies, hospitals, government entities, and medical professionals worldwide, and pursues collaboration and licensing arrangements with Pfizer, Otsuka, Ono, Nektar, AstraZeneca, Insitro, Schrödinger, and others. It also engages in partnerships for discovery and development with multiple biotech firms and academia. Founded in 1887 and headquartered in New York, the firm has a strong presence in immuno-oncology and focuses on innovative therapies and global reach.

Tom Garner

Senior Vice President, Head US Cardiovascular and Established Brands

Donald J. Hayden, Jr.

President

Brian Heaphy JD

Senior Vice President, Corporate Development

Dean J. Mitchell

President, International, President US Primary Care and Vice President, Strategy

107 past transactions

2seventy bio

Acquisition in 2025
22seventy bio is an immuno-oncology cell therapy company that discovers and develops cancer therapies. The company combines a deep knowledge of cancer cell biology and genetics with an understanding of the immune response to cancer to advance its pipeline. It was established in Cambridge, Massachusetts in 2021.

Be Biopharma

Series C in 2025
Founded in 2020, Be Biopharma specializes in developing innovative therapeutics using engineered B-cells to treat diseases such as cancer, autoimmune disorders, and infectious diseases. Its approach aims to overcome limitations of current cell and gene therapies.

Light Horse Therapeutics

Series A in 2025
Light Horse Therapeutics is a biotechnology company specializing in the application of gene editing to small-molecule drug discovery. It develops innovative methods to target the root causes of severe and life-threatening diseases, with an initial focus on challenging oncology targets. The company's advanced platform identifies critical functional domains within disease-related proteins, enabling the development of more effective therapies.

Bridgeway Behavioral Health Services

Grant in 2024
Bridgeway is an NJ State licensed nonprofit organization providing services to youth and adults experiencing mental health conditions.

Be Biopharma

Venture Round in 2024
Founded in 2020, Be Biopharma specializes in developing innovative therapeutics using engineered B-cells to treat diseases such as cancer, autoimmune disorders, and infectious diseases. Its approach aims to overcome limitations of current cell and gene therapies.

Prime Medicine

Corporate Round in 2024
Prime Medicine is a biotechnology company focused on developing genetic therapies using its innovative Prime Editing technology. This next-generation gene editing method allows for precise "search and replace" modifications in the genome, aimed at restoring normal genetic function. The company targets a wide range of diseases with significant unmet medical needs, leveraging the efficiency and versatility of its gene editing capabilities to address the underlying causes of these conditions. Through its commitment to advancing gene editing, Prime Medicine seeks to transform the landscape of genetic medicine.

Aktis Oncology

Series B in 2024
Aktis Oncology is a biotechnology company developing targeted radiopharmaceuticals for treating various solid tumor cancers. Its proprietary platforms generate tumor-targeting agents with optimal properties for alpha radiotherapy, ensuring high tumor penetration and long residence time to maximize tumor elimination while minimizing side effects.

Abata Therapeutics

Corporate Round in 2024
Abata Therapeutics is a biotechnology company dedicated to developing innovative cell therapies for patients suffering from progressive multiple sclerosis and other severe autoimmune and inflammatory diseases. The company specializes in the manipulation of regulatory T cells (Tregs) to address these conditions, aiming to restore balance within the immune system. By engineering Tregs to precisely target disease-related antigens, Abata Therapeutics creates therapies that can effectively treat diseases such as multiple sclerosis and type 1 diabetes without imposing systemic immune suppression. Founded by experts in immunology and cell therapy, Abata is committed to translating advanced scientific research into meaningful therapies that improve the lives of individuals facing chronic autoimmune challenges.

Roswell Park Cancer Institute

Grant in 2024
Roswell Park Cancer Institute (RPCI), established in 1898 by Dr. Roswell Park, is recognized as America's first cancer center. It pioneered a multidisciplinary approach to cancer treatment, emphasizing collaboration between scientists and clinicians, which has become the benchmark for modern comprehensive cancer centers. RPCI is one of the few facilities in upstate New York designated as a "comprehensive cancer center" by the National Cancer Institute and is a member of the National Comprehensive Cancer Network (NCCN). Faculty at RPCI are actively involved in developing Clinical Practice Guidelines in Oncology™, which are the internationally recognized standards for oncology clinical policy and are continually updated to reflect the latest advancements in cancer treatment.

Envisagenics

Series B in 2024
Envisagenics is a Huntington, New York-based company that develops a predictive analytics and bioinformatics platform to accelerate RNA therapeutics discovery. The cloud-based SpliceCore platform analyzes RNA sequencing data with artificial intelligence to identify splicing errors linked to disease, predict drug targets, and guide the design of RNA-based therapies. By translating transcriptomic insights into actionable targets, Envisagenics aims to reduce the time, cost, and risk of pharmaceutical development and to support partnerships with biopharma organizations. The firm focuses on uncovering RNA splicing alterations and translating them into therapeutic candidates, enabling researchers to validate targets and biomarkers more efficiently. The company originated as a spinout from Cold Spring Harbor Laboratory and emphasizes the use of AI and machine learning to simplify complex biomedical data for therapeutic discovery.

NeoPhore

Series B in 2024
NeoPhore Ltd is a biotechnology company based in Cambridge, United Kingdom, focused on the discovery and development of novel small molecule therapies for cancer treatment. Established in 2017, the company specializes in immuno-oncology therapeutics that aim to stimulate the immune system. NeoPhore's innovative therapies target genetic mechanisms to create neoantigens, which are recognized by the immune system as vulnerabilities within tumor cells. By exploiting these weak points, the company seeks to enhance clinical outcomes for cancer patients, providing a promising approach to cancer therapy.

Pathios Therapeutics

Series B in 2024
Pathios Therapeutics is an early-stage biotech company based in Oxford, United Kingdom, focused on developing therapies for autoimmune diseases and cancer. Founded in 2017, the company specializes in creating small molecule inhibitors that target the pH-sensing G protein-coupled receptor GPR65. These inhibitors are designed to counteract the immunosuppressive effects of immune cells, such as tumor-associated macrophages, which are influenced by the acidic environment often found in tumors. By leveraging a deep scientific approach and human genetic insights, Pathios Therapeutics aims to generate novel therapeutics for advanced solid tumors and other unmet medical needs.

Asher Bio

Series C in 2024
Asher Biotherapeutics, Inc. is a biotechnology company based in South San Francisco, California, founded in 2019. The company specializes in the development of immunotherapy drugs aimed at effectively treating cancer. Its innovative therapies are designed to enhance the immune system's ability to target and eliminate cancer cells while minimizing side effects. This focus allows healthcare providers to deliver effective treatments to patients in a shorter timeframe, aiming to improve overall outcomes in cancer care.

Nabla Bio

Series A in 2024
Nabla Bio is a biotechnology company that uses artificial intelligence and lab technologies to rationally design novel proteins for drug development. They aim to create medicines and improve nutrition by engineering proteins with enhanced qualities.

The Patients Association

Grant in 2024
The Patients Association is a non-profit organization. The organization provides medical, health, and social care services through a helpline, charity, and care home. Their customers' enquiries are addressed through phone, email, and online application.

Instituto Oncoguia

Grant in 2024
Instituto Oncoguia is a non-governmental organization and an interactive information portal dedicated to improving the quality of life for cancer patients, their families, and the general public. The organization provides educational content about various types of cancer, their symptoms, and treatments. It also offers guidance and support to people living with cancer, helping them navigate their journey. The information provided by Instituto Oncoguia is strictly educational and is not intended to replace medical consultation, tests, or treatment. The organization was established following the creation of the Oncoguia portal in 2003, in response to the clinical observation of the psychological needs of cancer patients.

Blood Cancer UK

Grant in 2024
Blood Cancer UK is a community dedicated to beating blood cancer by funding research and supporting those affected.

FED

Grant in 2024
FED is a non-profit organization that provides education, health, and migrant development services for the community.

Q32 Bio

Post in 2024
Q32 Bio is a clinical-stage biotechnology company focused on restoring healthy immune balance in autoimmune and inflammatory diseases by developing antibody-based therapies that modulate regulators of the innate and adaptive immune systems. Its development program includes ADX-914, a human anti-IL-7R antibody aimed at rebalancing adaptive immune function, and ADX-097, which demonstrates tissue-targeted distribution and durable pharmacokinetics/pharmacodynamics. Founded in 2017 and based in Cambridge, Massachusetts, the company emphasizes a team of scientists and immunology experts pursuing novel biologics to address diseases with limited or inadequate treatment options.

RayzeBio

Acquisition in 2024
RayzeBio, Inc. is a biotechnology company based in San Diego, California, founded in 2020. The company specializes in developing tumor-targeted small molecule medicines that leverage radioisotopes to improve cancer treatment outcomes. RayzeBio focuses on creating innovative radiopharmaceuticals, particularly utilizing alpha-emitting radioisotopes like Actinium-225, to target solid tumors effectively. With a robust pipeline of drug candidates, RayzeBio is committed to addressing significant market opportunities in oncology through late-stage clinical programs, development initiatives, and discovery efforts. The company's mission is to provide effective therapeutic solutions aimed at defeating cancer.

Attralus

Series B in 2024
Attralus, Inc. is a biopharmaceutical company dedicated to addressing the systemic nature of amyloidosis and enhancing the quality of life for affected patients. Incorporated in 2010 and headquartered in South San Francisco, California, Attralus develops proprietary peptide-based pan-amyloid targeting agents aimed at diagnosing and treating various forms and stages of systemic amyloidosis. Its product pipeline includes AT-01, a polybasic peptide radiotracer for diagnostic and monitoring purposes; AT-02, a peptide-immunoglobulin fusion for therapeutic use; and AT-03, an Fc-fusion protein designed for therapeutic applications. By targeting the common pathology present in all systemic amyloidosis diseases, Attralus seeks to create effective treatments for all subtypes, particularly those that currently lack available treatment options. The company was previously known as Aurora Bio, Inc., before rebranding in August 2020.

Cour Pharmaceuticals Development

Series A in 2024
Cour Pharmaceuticals Development Co Inc, founded in 2012 and based in Elmhurst, Illinois, operates in the pharmaceutical sector with a focus on developing an immune-modifying platform. This platform aims to achieve antigen-specific tolerance for immune-mediated diseases and provides non-biological therapeutics for conditions such as acute inflammation, autoimmunity, and allergies. The company is engaged in the pharmaceutical development of products related to immunology, pathology, and cardiovascular health, enabling the treatment of various conditions, including encephalitis syndromes, autoimmune disorders, infections, and heart attacks.

Ratio Therapeutics

Series B in 2024
Ratio Therapeutics develops radiotherapeutics to treat various cancers. Its proprietary platforms, Trillium and Macropa, enable the imaging, discovery, and advancement of novel radiopharmaceuticals for epithelial-derived cancers like breast, pancreatic, lung, colon, and others.

GlycoEra

Series A in 2024
GlycoEra is a biotechnology company focused on developing novel therapeutics by harnessing the power of glycan-mediated biology.

Karuna Therapeutics

Acquisition in 2023
Karuna Therapeutics is a biopharmaceutical company dedicated to developing innovative treatments for psychiatric and neurological disorders. Its primary focus is on creating novel therapies to address disabling neuropsychiatric conditions, with a particular emphasis on schizophrenia and the behavioral symptoms of Alzheimer's disease.

Health Coalition of Passaic County

Grant in 2023
Health Coalition of Passaic County provides data connectivity, analytics and reporting, community unification, and health care services.

Mirati Therapeutics

Acquisition in 2023
Mirati Therapeutics is a clinical-stage biotechnology company focused on developing cancer therapies. It concentrates on oncology, pursuing product candidates that address the genetic and immunological drivers of cancer. The company’s pipeline includes MRTX849, a KRAS G12C inhibitor in early-stage trials for non-small cell lung cancer, colorectal cancer, pancreatic cancer, and other tumors, and sitravatinib, a spectrum-selective kinase inhibitor in Phase II for non-small cell lung cancer, along with a KRAS G12D inhibitor program in preclinical development. Mirati collaborates with BeiGene to develop and commercialize sitravatinib and maintains a clinical collaboration with Novartis. Founded in 1995 and headquartered in San Diego, Mirati aims to translate insights into therapies that address high unmet medical needs in oncology.

AstronauTx

Series A in 2023
AstronauTx focuses on restoring healthy function of astrocytes, a type of brain cell crucial for neuronal health and blood-brain barrier integrity. Its primary goal is to develop treatments targeting astrocyte dysfunction in dementias like Alzheimer's disease.

Precede Biosciences

Series A in 2023
Precede Biosciences is breaking down the barriers to precision medicine by redefining what can be gleaned from a simple blood draw. Precede aims to increase drug development success rates and to contribute to a future in which every patient can receive a speedy, minimally invasive diagnosis and therapy tailored to the biology of their condition.

Drexel University

Grant in 2023
Founded in 1891, Drexel is a comprehensive global research university ranked among the top 100 in the U.S., with approximately 26,000 students. Known for its leadership in experiential learning through co-op programs and a history of academic technology firsts, Drexel offers over 200 degree programs across 15 colleges and schools. It is committed to being civically engaged, with community partnerships integrated into service and academics.

Cellares

Series C in 2023
Cellares Corporation, founded in 2019 and based in South San Francisco, California, specializes in the development of cell therapies for cancer treatment. The company addresses significant manufacturing challenges associated with these therapies, which are often produced on a per-patient basis, leading to high costs and limited availability. Cellares is pioneering the Cell Shuttle, an automated, closed end-to-end manufacturing solution designed to enhance the scalability and efficiency of cell therapy production. This innovative system allows for the simultaneous production of ten times more patient doses compared to traditional manual methods, while also reducing process failure rates by three-fold and lowering manufacturing costs by up to 70 percent. By providing flexible and scalable manufacturing options, Cellares aims to accelerate the delivery of life-saving therapies to patients in need and support the broader biopharmaceutical industry in meeting global demand for these treatments.

immatics biotechnologies

Post in 2023
immatics is a biopharmaceutical company focused on the discovery of true targets for cancer immunotherapies with the development of the right T cell receptors. The company's customized Adoptive Cell Therapies (ACTengine) and antibody-like TCR Bispecifics are the two main product classes in the pipeline (TCER). With a focus on particularly difficult-to-treat solid malignancies, each therapy modality has unique characteristics to create the desired therapeutic impact for patients at various disease stages and with various types of tumors. immatics biotechnologies was established in 2000 by Hans Rammensee, Harpreet Singh, and Steffen Walter in Tübingen, Baden-Wurttemberg.

K36 Therapeutics

Series B in 2023
K36 Therapeutics develops small molecule therapeutics for cancer treatment. It translates epigenetic modulation of oncogenic pathways into small molecule therapies.

TORL BioTherapeutics

Series B in 2023
TORL BioTherapeutics is a clinical-stage biopharmaceutical company dedicated to developing innovative, antibody-based therapies aimed at enhancing the lives of cancer patients. The company specializes in antibody-drug conjugates and other biologics, focusing on oncologic diseases with significant unmet medical needs. TORL BioTherapeutics employs a strategy that involves target identification and early discovery work, allowing them to selectively advance drug programs through novel licensing agreements. This approach enables their researchers to develop proprietary drugs with unique and optimized profiles, contributing to the advancement of cancer treatment options.

Outpace Bio

Series A in 2023
Outpace Bio is a biotechnology company that creates smart cell therapies aimed at improving efficacy and safety. It offers a platform that combines custom-designed biological functions with cellular control modalities that program the right response at the right time and place. It creates a mechanism-driven solution tailor-made to improve efficacy and safety. The company collaborates with Lyell Immunopharma to develop and commercialize a potential immune cell therapy for the treatment of cancer, auto-immune diseases, infectious diseases, degenerative diseases, regenerative medicine, metabolic disorders, and genetic disorders, enabling healthcare providers to cure a wide range of diseases as per patient's need.

Penn Medicine Princeton Cancer Center

Grant in 2023
Penn Medicine Princeton Cancer Center provides access to the specialist clinical services, rehabilitative care, and support required during cancer treatment and recovery from cancer.

Mediar Therapeutics

Series A in 2023
Mediar Therapeutics is a pre-clinical stage biotechnology company focused on developing therapeutics to treat fibrosis in chronically damaged organs. It designs antibodies that neutralize mediators driving fibrotic activity with the aim of halting and reversing fibrosis to improve patient outcomes. Founded in 2019 and based in Cambridge, Massachusetts, the company targets key fibrotic mediator proteins to address late-stage disease with precision and efficacy.

iVexSol

Series A in 2023
iVexSol specializes in developing and manufacturing lentiviral vectors (LVVs), which serve as critical gene delivery vehicles for cell and gene therapies. Founded in 2018, the company is headquartered in Worcester, Massachusetts. iVexSol's innovative technology addresses the shortage of LVVs by producing them in greater quantities and at a lower cost than traditional methods. This enables shorter clinical development timelines, increased access to life-saving treatments for patients worldwide.

Cajal Neuroscience

Series A in 2022
Cajal Neuroscience is a biotechnology company dedicated to discovering novel targets and therapeutics for neurodegeneration. It integrates human genetics, functional genomics, and advanced microscopy to accelerate drug discovery in this field.

Kura Oncology

Post in 2022
Kura Oncology is a clinical-stage biopharmaceutical company dedicated to developing precision medicines for cancer patients. Its pipeline comprises small molecule drug candidates targeting specific cancer signaling pathways, with a focus on solid tumors and hematologic malignancies.

SyntheX

Corporate Round in 2022
SyntheX specializes in drug discovery using synthetic biology platforms. It identifies protein interaction modulators and enables functional protein degradation, focusing on unique mechanisms for cancer and rare disease treatments.

Capstan Therapeutics

Series A in 2022
Capstan Therapeutics specializes in developing innovative therapeutics using precision cell engineering for various diseases with unmet clinical needs.

Autobahn Therapeutics

Venture Round in 2022
Autobahn Therapeutics develops brain-targeting, small molecule therapies for central nervous system disorders. Its lead program ABX-002 is a thyroid hormone receptor beta agonist being developed as an adjunctive treatment for mood disorders, including major depressive disorder and bipolar depression. The company emphasizes precision tuning of CNS exposure, validated clinical and biologic targets, and biomarker-guided development across neuropsychiatry, neurodegeneration, and neuroinflammation to address high unmet medical needs and improve patient outcomes.

BigHat Biosciences

Series B in 2022
BigHat Biosciences is a biotechnology company that develops an AI-guided platform for designing and characterizing antibodies and other therapeutic proteins. The platform combines a wet laboratory with artificial intelligence and machine learning to enable antibody discovery and optimization, helping drug developers create antibodies and novel biotherapeutic designs. It emphasizes multi-objective, data-driven workflows to improve safety, biophysical properties, and efficacy of antibody candidates. Founded in 2019 and based in San Carlos, California.

Owkin

Series B in 2022
Founded in 2016, Owkin is a French-American startup that uses artificial intelligence to enhance medical research. It develops machine learning tools to understand complex biology, identify new treatments, de-risk clinical trials, and develop diagnostics. Owkin's focus is improving drug discovery processes and patient outcomes.

Turning Point Therapeutics

Acquisition in 2022
Turning Point Therapeutics is a clinical-stage biopharmaceutical company focused on designing and developing novel small molecule targeted oncology therapies. Its pipeline includes repotrectinib, TPX-0046, TPX-0022, and preclinical ALK inhibitor TPX-0131, targeting genetic drivers of cancer in TKI-naïve and TKI-pretreated patients.

Transition Bio

Series A in 2022
Transition Bio, Inc. is a biotechnology company dedicated to advancing human health through the discovery, analysis, and modulation of biological condensates. Founded in 2020 and based in Cambridge, Massachusetts, with a branch in Cambridge, United Kingdom, the company has developed a hypothesis-free drug discovery and diagnostics platform known as Condensomics. This innovative platform leverages droplet microfluidic technologies and protein biophysics to study condensates with remarkable precision, providing medical practitioners with detailed molecular mappings. Transition Bio's approach is designed to unlock new opportunities for drug development, setting it apart in the biopharmaceutical landscape.

Sapience Therapeutics

Series B in 2022
Sapience Therapeutics, Inc. is a biotechnology company focused on discovering and developing peptide-based therapeutics aimed at addressing high mortality cancers. Founded in 2015 and headquartered in Harrison, New York, the company is advancing novel therapies to meet significant unmet medical needs. Its lead product, ST101, is an inhibitor of the transcription factor C/EBPß, which is overexpressed in various cancers and plays a critical role in cellular differentiation, tumor survival, and proliferation. ST101 reduces the expression of several target genes and proteins associated with cancer cell survival and growth, inducing selective cytotoxicity in tumor types such as breast cancer, melanoma, prostate cancer, glioblastoma multiforme, lung cancer, and acute myeloid leukemia. The company aims to develop first-in-class treatments for deadly conditions, with a particular focus on glioblastoma, the most aggressive form of brain cancer.

Nuvig Therapeutics

Series A in 2022
Nuvig Therapeutics focuses on developing innovative therapies aimed at restoring immune homeostasis and rebalancing immune function. The company is dedicated to creating a pipeline of novel immune therapeutics specifically targeting chronic inflammatory and autoimmune diseases. By harnessing natural mechanisms to modulate immune responses, Nuvig seeks to enhance treatment options for patients, ultimately improving their health outcomes.

Octant Bio

Series B in 2022
Octant Bio is a company focused on developing synthetic technology to enhance health and treat diseases. The firm employs synthetic biology, genome engineering, next-generation sequencing, and computational tools to measure the activity of thousands of receptor pathways in human cells simultaneously. This approach allows scientists to use machine learning methods to engineer small molecules that can interact with multiple receptors, offering new potential for treating complex diseases.

Be Biopharma

Series B in 2022
Founded in 2020, Be Biopharma specializes in developing innovative therapeutics using engineered B-cells to treat diseases such as cancer, autoimmune disorders, and infectious diseases. Its approach aims to overcome limitations of current cell and gene therapies.

Ceptur Therapeutics

Series A in 2022
Ceptur Therapeutics is focused on developing innovative genetic medicines for patients with unmet medical needs. The company utilizes its proprietary U1 Adaptor technology to achieve non-genotoxic, long-lasting silencing of disease-causing genes, particularly in challenging tissues beyond the liver and central nervous system. This technology addresses the limitations of existing gene silencing methods and has potential applications in cancer treatment, allowing healthcare providers to offer new therapeutic options for various cancer types. Through its advancements, Ceptur aims to improve patient outcomes by providing effective solutions for difficult-to-treat conditions.

Century Therapeutics

Post in 2022
Century Therapeutics is a biotechnology company developing allogeneic cell therapies derived from induced pluripotent stem cells to treat cancer and related diseases. Its platform enables engineering of iPSCs into NK and T cells with master cell banks of modified cells that can be expanded and differentiated into standardized, off-the-shelf therapies. The company combines CRISPR-mediated gene editing, proprietary chimeric antigen receptors, Allo-Evasion technology, and manufacturing capabilities to enable scalable production of homogeneous cell products for hematologic and solid tumors. While focused on oncology, its platform also targets autoimmune and inflammatory diseases with the goal of improving cell therapy performance and reducing host immune rejection.

Compugen

Post in 2021
Compugen is a clinical-stage therapeutic discovery and development company based in Israel. It utilizes predictive computational capabilities to identify novel drug targets and biological pathways, focusing on cancer immunotherapy. Its immuno-oncology pipeline includes four clinical-stage programs targeting immune checkpoints.

Clade Therapeutics

Series A in 2021
Founded in 2020, Clade Therapeutics is a biopharmaceutical company headquartered in Cambridge, Massachusetts. It specializes in developing scalable, off-the-shelf stem-cell-based therapies to treat cancer, autoimmune diseases, and other life-threatening conditions.

Nitrase Therapeutics

Series A in 2021
Nitrase Therapeutics is a biopharmaceutical company developing therapies against a novel class of enzymes called nitrases, initially focusing on Parkinson’s disease. Its proprietary platform enables the identification and targeting of these enzymes to potentially slow or halt disease progression.

TreeFrog Therapeutics

Series B in 2021
TreeFrog Therapeutics is a stem cell company focused on scalable production of stem cells for cell therapies. It develops and uses a proprietary end-to-end 3D bioreactor-based platform called C-Stem to enable scalable, cGMP-compliant manufacturing. Founded in 2018 and based in Pessac, France, the company aims to secure cell production and quality, accelerate clinical development, and improve market access by reducing treatment costs. The platform addresses manufacturing bottlenecks in the cell therapy sector, offering an integrated solution from cell culture to manufacturing readiness to support safe, affordable stem cell therapies.

Cardior Pharmaceuticals

Series B in 2021
Cardior Pharmaceuticals GmbH is a biotechnology company based in Hanover, Germany, founded in 2016. The company specializes in developing non-coding RNA-based therapeutics aimed at treating and preventing heart disease, which is the leading cause of death in the western world. Its primary focus is on CDR-132X, an oligonucleotide-based inhibitor that targets a critical microRNA responsible for pathological changes in the heart resulting from stress or injury. Through its innovative approach, Cardior Pharmaceuticals seeks to address significant unmet medical needs in cardiovascular health.

IMIDomics

Series A in 2021
IMIDomics is a specialized company focused on addressing Immune-Mediated Inflammatory Diseases (IMIDs). It operates by leveraging the world's largest biobank dedicated to IMIDs, alongside its extensive clinical expertise and advanced genomic analysis capabilities. The company develops an analytical platform that provides healthcare professionals with accessible insights from vast amounts of molecular and clinical data, facilitating optimized treatment strategies for patients with IMIDs. With locations at Vall d'Hebron Hospital in Barcelona, Spain, and the HudsonAlpha Institute in Huntsville, Alabama, IMIDomics aims to advance the understanding and management of these complex diseases through innovative biomarker discovery and application.

Allyx Therapeutics

Venture Round in 2021
Allyx Therapeutics, Inc. is a clinical-stage biotechnology company founded in 2018 and based in Durham, Connecticut. The company specializes in developing disease-modifying treatments for Alzheimer's Disease, with a focus on reversing neurodegeneration. Its lead product is an orally bioavailable small molecule that functions as a silent allosteric modulator of mGluR5. This innovative approach aims to provide clinicians with a therapeutic option capable of preserving cognition in patients while addressing the underlying disease mechanisms.

HiberCell

Series B in 2021
Founded in 2019, HiberCell is a biotechnology company based in New York. It develops therapeutics focused on preventing cancer relapse and metastasis by targeting adaptive stress pathways and immune modulation.

Aktis Oncology

Series A in 2021
Aktis Oncology is a biotechnology company developing targeted radiopharmaceuticals for treating various solid tumor cancers. Its proprietary platforms generate tumor-targeting agents with optimal properties for alpha radiotherapy, ensuring high tumor penetration and long residence time to maximize tumor elimination while minimizing side effects.

Exscientia

Series C in 2021
Exscientia is a biotechnology company that leverages artificial intelligence and machine learning to enhance the discovery and design of novel therapeutic compounds. By integrating human expertise with advanced computational techniques, Exscientia accelerates the development of small-molecule drug candidates, aiming to produce safe and effective treatments for clinical testing. The company's innovative approach seeks to revolutionize the pharmaceutical industry by improving the precision and efficiency of drug discovery, ultimately enhancing patient outcomes.

Presage Biosciences

Venture Round in 2021
Presage Biosciences, Inc. is an oncology company based in Seattle, Washington, that focuses on enhancing drug development and clinical trials through innovative technology. Founded in 2008, the company has developed the CIVO arrayed microinjection platform, which allows for the simultaneous assessment of multiple drugs or drug combinations directly within a patient's tumor. This method provides insights into drug efficacy, resistance, and potential synergies in the tumor's native microenvironment, thereby overcoming limitations associated with systemic drug administration. By using this clinical surrogate approach, Presage enables drug developers to identify ineffective compounds early in the process, ultimately streamlining the development of effective cancer treatments. The technology also facilitates the identification of drug targets and effective combinations, allowing for more accurate measurement of therapeutic responses.

Orna Therapeutics

Series A in 2021
Orna Therapeutics is a biotechnology company focused on designing and delivering fully engineered circular RNA (oRNA) therapeutics. Its platform combines engineered circular RNA constructs that drive protein expression with delivery solutions, notably lipid nanoparticles, to enable safe and effective in vivo therapies. The approach expands therapeutic possibilities across diseases such as oncology, autoimmune diseases, and infectious diseases. Established in 2019 and based in Cambridge, Massachusetts, Orna Therapeutics pursues therapies built on oRNA constructs designed to express therapeutic proteins in a controlled manner.

Ikena Oncology

Series B in 2021
Ikena Oncology, Inc. is a biotechnology company focused on discovering and developing biomarker-driven therapies for cancer treatment. It specializes in precision oncology by targeting pathways essential for cancer growth and therapeutic resistance, particularly within the Hippo and RAS signaling networks. The company's portfolio includes several preclinical and discovery-stage programs, such as IK-007, an EP4 receptor antagonist; IK-175, an AHR antagonist; and IK-412, a kynurenine-degrading enzyme. Additionally, Ikena is developing IK-930, an oral small-molecule inhibitor of the TEAD transcription factor involved in the Hippo pathway. Ikena Oncology, originally founded as Kyn Therapeutics in 2016, rebranded in December 2019 and is headquartered in Boston, Massachusetts. The company aims to address significant medical needs in oncology through innovative drug development.

MyoKardia

Acquisition in 2020
MyoKardia, Inc. is a clinical-stage biopharmaceutical company based in Brisbane, California, specializing in the discovery, development, and commercialization of targeted therapies for rare cardiovascular diseases. Founded in 2012, the company focuses on heritable cardiomyopathies and genetically-driven heart failure stemming from biomechanical defects in cardiac muscle contraction. Its lead product candidate, Mavacamten, is an orally administered allosteric modulator of cardiac myosin currently undergoing Phase III clinical trials for hypertrophic cardiomyopathy (HCM). Additionally, MyoKardia is developing Danicamtiv, which has completed Phase I and IIa trials for dilated cardiomyopathy, alongside several preclinical programs targeting related cardiovascular conditions. As of November 2020, MyoKardia operates as a subsidiary of Bristol-Myers Squibb Company.

Forbius

Acquisition in 2020
Forbius, also known as Formation Biologics, is a clinical-stage biopharmaceutical company focused on designing and developing innovative therapeutics for cancer and fibrotic diseases. Founded in 2011 as a management-led spin-out from YM BioSciences, the company specializes in creating agents that target critical biological pathways, specifically the transforming growth factor-beta (TGF-beta) and epidermal growth factor receptor (EGFR) pathways. By leveraging advanced protein engineering technologies and a deep understanding of biology, Forbius aims to produce highly effective inhibitors with unique mechanisms of action, ultimately striving to improve patient outcomes and transform lives.

Autobahn Therapeutics

Series B in 2020
Autobahn Therapeutics develops brain-targeting, small molecule therapies for central nervous system disorders. Its lead program ABX-002 is a thyroid hormone receptor beta agonist being developed as an adjunctive treatment for mood disorders, including major depressive disorder and bipolar depression. The company emphasizes precision tuning of CNS exposure, validated clinical and biologic targets, and biomarker-guided development across neuropsychiatry, neurodegeneration, and neuroinflammation to address high unmet medical needs and improve patient outcomes.

Exscientia

Series C in 2020
Exscientia is a biotechnology company that leverages artificial intelligence and machine learning to enhance the discovery and design of novel therapeutic compounds. By integrating human expertise with advanced computational techniques, Exscientia accelerates the development of small-molecule drug candidates, aiming to produce safe and effective treatments for clinical testing. The company's innovative approach seeks to revolutionize the pharmaceutical industry by improving the precision and efficiency of drug discovery, ultimately enhancing patient outcomes.

Silverback Therapeutics

Series B in 2020
Silverback Therapeutics, Inc. is a clinical-stage biopharmaceutical company based in Seattle, Washington, specializing in the development of tissue-targeted therapeutics aimed at treating cancer, chronic viral infections, and other serious diseases. The company’s lead product candidate, SBT6050, is currently in a Phase I/Ib clinical trial and is designed as a TLR8 agonist linker-payload conjugated to a HER2-directed monoclonal antibody, targeting tumors such as breast and non-small cell lung cancers. Silverback is also advancing SBT6290, a preclinical candidate targeting Nectin4 in various cancers, and SBT8230, which aims to treat chronic hepatitis B virus infection. The company employs its proprietary ImmunoTAC technology platform to create therapies that can be systemically administered while acting specifically at disease sites, thereby potentially modulating fundamental disease pathways previously considered inaccessible. Founded in 2016, Silverback Therapeutics is committed to innovative approaches in biopharmaceutical development.

Celgene

Acquisition in 2019
Celgene Corporation is a global biopharmaceutical company focused on the discovery, development, and commercialization of innovative therapies for cancer and immune-inflammatory diseases. The company aims to provide treatment options for patients with limited alternatives, conducting numerous clinical trials at major medical centers for its investigational compounds. Celgene's research primarily targets incurable hematological cancers, such as multiple myeloma, chronic lymphocytic leukemia, and non-Hodgkin’s lymphoma, as well as solid tumors like pancreatic cancer and melanoma. Additionally, the company is developing therapies for serious inflammatory conditions, including psoriasis and psoriatic arthritis. With a commitment to improving patient outcomes, Celgene continues to advance its pipeline of biopharmaceutical drugs.

PathAI

Series B in 2019
PathAI, Inc. is a technology company that specializes in developing artificial intelligence solutions for pathology laboratories. Founded in 2016 and headquartered in Boston, Massachusetts, with an additional office in Austin, Texas, PathAI focuses on enhancing the accuracy and efficiency of cancer diagnosis and treatment. The company's platform employs machine and deep learning techniques to analyze large datasets, assisting pathologists in making rapid and precise diagnoses for patients. By addressing complex challenges in pathology, PathAI aims to facilitate personalized medicine and improve patient outcomes by identifying individuals who may benefit from innovative therapies.

Vedanta Biosciences

Series C in 2019
Vedanta Biosciences is a clinical-stage microbiome company focused on developing therapies for immune-mediated and infectious diseases using live bacteria derived from the human microbiome. The company designs orally delivered defined bacterial consortia, leveraging libraries of microbiome-derived strains, proprietary datasets from human interventional studies, and tools for selecting potent strains. Its platform encompasses consortium design and CGMP manufacturing of bacterially defined products, enabling physicians to access live bacteria drugs for autoimmune and inflammatory conditions. Headquartered in Cambridge, Massachusetts, Vedanta Biosciences aims to create a new category of oral therapies arising from defined bacterial communities grown from clonal cell banks.

Celgene

Acquisition in 2019
Celgene Corporation is a global biopharmaceutical company focused on the discovery, development, and commercialization of innovative therapies for cancer and immune-inflammatory diseases. The company aims to provide treatment options for patients with limited alternatives, conducting numerous clinical trials at major medical centers for its investigational compounds. Celgene's research primarily targets incurable hematological cancers, such as multiple myeloma, chronic lymphocytic leukemia, and non-Hodgkin’s lymphoma, as well as solid tumors like pancreatic cancer and melanoma. Additionally, the company is developing therapies for serious inflammatory conditions, including psoriasis and psoriatic arthritis. With a commitment to improving patient outcomes, Celgene continues to advance its pipeline of biopharmaceutical drugs.

Vedanta Biosciences

Series C in 2018
Vedanta Biosciences is a clinical-stage microbiome company focused on developing therapies for immune-mediated and infectious diseases using live bacteria derived from the human microbiome. The company designs orally delivered defined bacterial consortia, leveraging libraries of microbiome-derived strains, proprietary datasets from human interventional studies, and tools for selecting potent strains. Its platform encompasses consortium design and CGMP manufacturing of bacterially defined products, enabling physicians to access live bacteria drugs for autoimmune and inflammatory conditions. Headquartered in Cambridge, Massachusetts, Vedanta Biosciences aims to create a new category of oral therapies arising from defined bacterial communities grown from clonal cell banks.

Galecto

Series C in 2018
Galecto is a clinical-stage biotechnology company developing small molecule therapeutics targeting galectin-3 and lysyl oxidase-like 2 for treating severe diseases like fibrosis and cancer. Its lead product candidate, GB0139, is an inhaled inhibitor of galectin-3 for treating severe fibrotic lung diseases such as idiopathic pulmonary fibrosis.

Compugen

Post in 2018
Compugen is a clinical-stage therapeutic discovery and development company based in Israel. It utilizes predictive computational capabilities to identify novel drug targets and biological pathways, focusing on cancer immunotherapy. Its immuno-oncology pipeline includes four clinical-stage programs targeting immune checkpoints.

Avera PACE

Grant in 2018
Avera PACE, a division of Avera Health, operates as a regional group-purchasing organization primarily serving clients in the upper Midwest but extending its services across the United States. The organization focuses on providing access to cost-effective contracts, services, and products, benefiting businesses located in both metropolitan and rural areas. By promoting collaboration, utilization, and continuous improvement, Avera PACE helps its clients achieve lower operational costs. Additionally, Avera Medical Group, part of Avera Health, offers a wide range of healthcare services including behavioral health, cancer care, cardiology, pediatrics, emergency care, surgery, neuroscience, and women's health, further enhancing the value and support available to the communities it serves.

Personal Genome Diagnostics

Series B in 2018
Personal Genome Diagnostics, Inc. is a biotechnology company focused on patient-specific analyses of cancer genomes. Established in 2010 and headquartered in Baltimore, Maryland, the company has pioneered technologies for non-invasive "liquid biopsy" approaches, allowing for the detection of tumor-specific alterations in circulating cell-free DNA. Its offerings include the METDetect Assay for identifying MET gene amplifications, LungSelect for detecting actionable genetic alterations in non-small cell lung cancer patients, and PGDx elio plasma resolve, which analyzes various genetic mutations from plasma samples. Additionally, Personal Genome Diagnostics provides RNAcomplete, enabling researchers to extract both RNA and genomic DNA from a single tissue sample, and CancerXOME, which captures and analyzes coding regions of genes. The company collaborates with institutions like Mayo Clinic and partners with KingMed Diagnostics to enhance its research and diagnostic capabilities, thereby empowering oncologists and researchers with crucial genomic insights to combat cancer.

Enterome

Debt Financing in 2018
Enterome develops innovative cancer treatments focusing on generating powerful, long-lasting immune responses using its proprietary OncoMimic technology. The company aims to overcome immune tolerance against cancer cells, with applications across various solid tumors. Its most advanced programs are in Phase 2 clinical trials for hard-to-treat tumors such as glioblastoma, adrenal malignancies, and colorectal cancer.

TARIS Biomedical

Series B in 2017
TARIS Biomedical, Inc. is a therapeutically focused urology company based in Lexington, Massachusetts, established in 2008. The company specializes in developing innovative treatments for challenging bladder diseases, including bladder cancer and overactive bladder. TARIS Biomedical's proprietary system is designed to continuously release medications directly into the bladder over extended periods, ranging from weeks to months. This technology is administered through minimally invasive, in-office procedures, allowing for customized drug delivery that aligns with the specific needs of various bladder conditions. As of December 2019, TARIS Biomedical operates as a subsidiary of Janssen Research & Development, LLC.

Jefferson Health System

Grant in 2017
Jefferson Health System is a healthcare organization that focuses on delivering high-quality medical services to its patients. The system operates a network of hospitals, outpatient centers, and physician practices in the Philadelphia area. With a commitment to providing patient-centered care, Jefferson Health System offers a wide range of medical specialties and services to meet the diverse needs of its community. Through collaboration with healthcare professionals and cutting-edge research, the organization strives to improve the health and well-being of individuals in the region. Jefferson Health System aims to be a leader in the healthcare industry by maintaining a strong reputation for excellence in patient care and innovation.

Akamis Bio

Venture Round in 2017
Akamis Bio is a clinical-stage oncology company dedicated to improving cancer patient outcomes through its innovative Tumor-Specific Immuno-Gene Therapy (T-SIGn®) platform. The company develops therapeutics that enable the immune system to recognize and clear solid tumors.

University of North Carolina at Chapel Hill School of Medicine

Grant in 2017
The University of North Carolina at Chapel Hill School of Medicine is a professional school within the university that offers degrees in medicine, allied health sciences, and biomedical sciences, including combined programs such as MD/PhD, MD/MPH, and MD/MBA. It aims to improve health and wellbeing by providing leadership and excellence in patient care, education, and research, while fostering a diverse, respectful environment that supports faculty, staff, and learners. The school houses centers focused on health equity and aging and health, including the UNC Center for Health Equity Research, which advances health in underserved communities through research collaborations, and the UNC Center for Aging and Health, which delivers high-quality clinical care to older adults, connects families with resources, and trains the next generation of geriatric professionals.

IFM Therapeutics

Acquisition in 2017
IFM Therapeutics is a biotechnology company focused on developing small-molecule medicines that modulate the innate immune system to treat inflammatory and autoimmune diseases and cancer. Its approach combines in-house discovery with collaborations to target novel components of innate immunity. The company operates through subsidiaries and affiliates, including IFM Due, which concentrates on antagonists of the cGAS/STING pathway for inflammation, neuroinflammation, autoimmunity, and cancer, and IFM Discovery, an incubator pursuing a portfolio of genetically validated targets as next-generation therapies for inflammation, neuroinflammation, autoimmunity, and fibrosis. By designing small molecules that precisely engage innate immune targets, IFM Therapeutics aims to improve patient immune responses and address difficult therapeutic areas.

Cardior Pharmaceuticals

Series A in 2017
Cardior Pharmaceuticals GmbH is a biotechnology company based in Hanover, Germany, founded in 2016. The company specializes in developing non-coding RNA-based therapeutics aimed at treating and preventing heart disease, which is the leading cause of death in the western world. Its primary focus is on CDR-132X, an oligonucleotide-based inhibitor that targets a critical microRNA responsible for pathological changes in the heart resulting from stress or injury. Through its innovative approach, Cardior Pharmaceuticals seeks to address significant unmet medical needs in cardiovascular health.

Enterome

Series D in 2017
Enterome develops innovative cancer treatments focusing on generating powerful, long-lasting immune responses using its proprietary OncoMimic technology. The company aims to overcome immune tolerance against cancer cells, with applications across various solid tumors. Its most advanced programs are in Phase 2 clinical trials for hard-to-treat tumors such as glioblastoma, adrenal malignancies, and colorectal cancer.

Cormorant Pharmaceuticals

Acquisition in 2016
Cormorant Pharmaceuticals is a privately held biopharmaceutical company located at the Karolinska Institute Science Park in Stockholm, Sweden. Founded by Maarten de Château and Urban Paulsson, the company specializes in the development of therapeutics for cancer and other rare diseases. Cormorant has focused its efforts on HuMax-IL8, a fully human monoclonal antibody acquired from Genmab A/S. This drug is based on research indicating that interleukin-8 (IL-8) plays a significant role in the progression of malignant tumors. Through its innovative approach, Cormorant Pharmaceuticals aims to address critical unmet medical needs in oncology and rare disease treatment.

Blade Therapeutics

Series B in 2016
Blade Therapeutics is a discovery-stage drug development company focused on creating antifibrotic treatment strategies for a range of congenital and acquired fibrotic diseases. The company aims to revolutionize the treatment of these conditions by addressing their underlying pathophysiology, potentially reversing tissue damage caused by fibrosis. With a leadership team experienced in drug development for fibrotic disorders, Blade Therapeutics collaborates with international experts to identify and in-license innovative technologies, thereby building a robust pipeline of antifibrotic compounds. Their therapies are designed to offer effective treatment options that minimize side effects for patients suffering from fibrotic diseases.

Padlock Therapeutics

Acquisition in 2016
Padlock Therapeutics is a biotechnology company focused on developing innovative medicines that target protein-arginine deiminases (PADs), which are enzymes involved in the generation of autoantigens and play a significant role in inflammation and immune responses associated with autoimmune diseases. The company aims to investigate the biological and therapeutic implications of protein deimination by PADs. Founded by scientists from The Scripps Research Institute in collaboration with members of the Atlas Venture Life Sciences Team, Padlock operates as a seed-stage company based in Cambridge, Massachusetts. Its investors include prominent names such as Atlas Venture, Johnson & Johnson, and MS Ventures.

Cardioxyl Pharmaceuticals

Acquisition in 2015
Cardioxyl Pharmaceuticals is a clinical stage biopharmaceutical company focused on developing innovative therapies for cardiovascular disease. The company is dedicated to discovering, developing, and commercializing novel technologies in areas where existing treatments are lacking or inadequate. With a strong emphasis on nitroxyl technology, Cardioxyl has established significant expertise in its chemistry, biology, and clinical applications. The company's leading candidate, CXL-1020, is currently undergoing clinical development for Acute Decompensated Heart Failure, a condition that is a primary cause of hospitalization among patients over the age of 65. Through its research and development efforts, Cardioxyl aims to address critical unmet needs in cardiovascular care.

Flexus Biosciences

Acquisition in 2015
Flexus Biosciences, established in 2013 and based in San Carlos, California, is a privately-held biopharmaceutical company dedicated to developing innovative small-molecule cancer therapeutics. Its primary focus lies in targeting regulatory T cells, aiming to create novel immunotherapies that enhance the body's immune response against cancer.

iPierian

Acquisition in 2014
iPierian is a biotechnology company specializing in the development of therapies for neurodegenerative diseases. Utilizing induced pluripotent stem cells, the company focuses on addressing significant unmet medical needs, particularly in conditions such as spinal muscular atrophy, amyotrophic lateral sclerosis, and Parkinson's disease. iPierian is engaged in the research and development of innovative therapies, including monoclonal antibodies aimed at treating Alzheimer's disease and other Tauopathies. By targeting the mechanisms that drive disease progression, the company aims to provide physicians with effective tools to slow the spread of Tau in the brain, thereby potentially improving patient outcomes.

Amylin Pharmaceuticals

Acquisition in 2012
Amylin Pharmaceuticals is a biopharmaceutical company focused on the discovery, development, and commercialization of innovative drugs aimed at treating diabetes, obesity, and other related diseases. The company is known for its flagship product, BYDUREON, a weekly treatment designed for adults with type 2 diabetes to enhance glycemic control in conjunction with diet and exercise. Amylin has also developed a dual chamber cartridge pen configuration for BYDUREON, enabling patients to mix and administer the medication conveniently from a pre-filled pen device. With a commitment to advancing diabetes care, Amylin Pharmaceuticals aims to challenge scientific boundaries and improve the lives of individuals affected by these conditions.

Inhibitex

Acquisition in 2012
Inhibitex is a biotechnology company that specializes in the development of antibody-based products aimed at preventing and treating bacterial and fungal infections. The company is particularly focused on creating small molecule antiviral compounds, with specific attention to therapies for shingles, also known as herpes zoster, and chronic hepatitis C infections. Through its innovative approach, Inhibitex seeks to address significant medical needs in the realm of infectious diseases.

Amira Pharmaceuticals

Acquisition in 2011
Amira Pharmaceuticals is a small molecule pharmaceutical company dedicated to the discovery and early development of innovative drugs for treating inflammatory diseases. The company leverages its team’s expertise in bioactive lipid pathways and complex signaling processes to address various conditions, including asthma, chronic obstructive pulmonary disease, cardiovascular diseases, and fibrotic diseases. Through its focused research efforts, Amira Pharmaceuticals aims to create effective therapeutic solutions that can significantly improve patient outcomes in these areas.

ZymoGenetics

Acquisition in 2010
ZymoGenetics is a biotechnology company dedicated to the discovery, development, and early manufacturing of therapeutic proteins aimed at treating human diseases. As a fully-integrated research and development organization, it possesses a diverse array of competencies, including molecular and cellular biology, protein chemistry, and antibody generation and engineering. The company is actively involved in the clinical development and operations of its products and addresses regulatory affairs and quality control. ZymoGenetics is known for its therapeutic pipeline, which includes recothrom, a protein designed for hemostasis, underscoring its commitment to advancing innovative treatments in the biopharmaceutical sector.

CareDx

Series G in 2009
CareDx is a molecular diagnostics company specializing in noninvasive surveillance tests to identify post-transplant injuries and rule out rejection, supporting the entire transplant journey from initial matching to patient care.

Medarex

Acquisition in 2009
Medarex is a biopharmaceutical company dedicated to the discovery, development, and potential commercialization of fully human antibody-based therapeutics aimed at treating life-threatening and debilitating diseases, such as cancer, inflammation, autoimmune disorders, and infectious diseases. The company leverages its UltiMAb technology, along with its expertise in product development and clinical manufacturing, to create and support a diverse range of fully human antibody product candidates. Medarex focuses on advancing these therapeutics for both its own portfolio and in collaboration with partners in the biopharmaceutical industry.
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