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Immunova is a startup with  an IP portfolio licensed from Yale and the Johns Hopkins Universities.

Immunova's technology platform has a unique capability to deliver one or more drugs to the tumor/disease microenvironment. The drugs can be proteins, small molecules or nucleic acids. The delivery platfrom has demonstatable advantages over other delivery systems. The technology has applications in oncology and inflammation.

The company's lead asset is positioned in oncology. IMM-01, consists of two drugs that (a) undermine the tumor micorenvironment and (b) increase anti-tumor cell mediated immunity. This asset is capable of curing mice of metastatic disease. Further, it significantly enhances the activites of immune checkpoint inhibitors. It is non toxic.

The company is seeking investment and R&D partners. Immunova has defined the path to a Phase I/IIa multidose trial which could initiate within 15 months of funding. Immunova is also seeking partners who wish to validate this platform in oncology and inflammation.

Aperiomics, Inc. is a next generation sequencing service company with a mission to detect virtually any pathogen from any clinical, agricultural, or environmental sample.  This service platform uses a combination of next-generation sequencing and advanced bioinformatic data analysis to identify pathogens in various samples.  Aperiomics’ proprietary service platform focuses on pathogens of public and animal health importance, satisfying the increasing need for more robust and more efficient next-generation sequencing data analysis.

The impact of Aperiomics’ technologies is broad due to our unique approach to pathogen detection. Instead of blindly probing for a proverbial ‘needle in a haystack’, Aperiomics’ approach analyzes the entire ‘haystack’ using next-generation sequencing and harnessing the power of bioinformatics to identify all ‘needles’. This approach is transformative compared to current pathogen detection methods. Aperiomics’ proprietary service, Absolute*NGS Pathogen Detection Platform, screens samples (clinical, environmental, etc.) for the presence of any microbe (fungal, viral, bacterial, eukaryotic parasite) – including pathogens that have never before been identified. This platform technology has broad application across diverse markets such as health care, agriculture, environmental, industrial, and veterinary testing.

Kineta® is a nationally-recognized biotechnology company focused on developing leading edge therapeutics in three large high need therapeutic areas: autoimmune disease, viral disease and chronic pain. Our company is focused on the development of novel drug candidates each the outcome of years of scientific exploration and supported by an extensive body of peer-reviewed NIH-supported research.

MP Healthcare Ventures is the corporate venture arm of Mitsubishi Tanabe Pharma founded in 2006 and based in Boston Massachusetts. The firm is looking to provide equity capital to seed and venture stage companies in the life science space. The firm is looking to provide companies with $5 million over the lifetime of the investment and plans on making 2-3 investments over the next year. The firm will invest in companies located anywhere around the world.

Crestone, Inc. is an early stage drug discovery and development company focused on developing novel treatments for serious bacterial infections.  The company currently has two main programs that address areas of significant and growing unmet medical need, both with novel mechanism of action agents.

1.         Novel treatment for Clostridium difficile infections.  CRS3123 is currently in clinical development for the treatment of C. difficile infection (CDI), and is nearing completion of Phase 1.  CDI occurs when toxin-producing bacteria colonize the gastrointestinal tract.  The infection spreads rapidly via spores which contaminate hospitals and nursing homes, and recurrence is a major clinical issue.  Due to the emergence of hyper-virulent drug resistant strains, mortality from CDI has increased over 700% since 1999.  In preclinical studies, CRS3123 shows much lower recurrence compared to vancomycin, a key attribute for improved therapy of CDI.  We seek funding for Phase 2 clinical studies to demonstrate clinical proof-of-concept.

2.         Novel oral agents for Gram-positive infections.  We are developing a novel class of DNA replication inhibitors, currently in advanced preclinical research.  These compounds selectively inhibit an essential component of the replicative DNA polymerase complex and are potent, orally available, and effective against all clinically-relevant Gram-positive pathogens, including methicillin-resistant Staphylococcus aureus (MRSA), vancomycin-resistant enterococci (VRE), penicillin-resistant Streptococcus pneumoniae (PRSP) and Bacillus anthracis (anthrax).  We anticipate development of a drug similar to Zyvox in spectrum, but with key advantages such as rapid bacterial killing and improved safety.  This grant-supported program is expected to produce a clinical candidate in 2015.   

Crestone will develop these programs through key value inflection points in early clinical development, and then share the risk and expense of late-stage trials with a partner.  We have a talented core team in place, and have a plan for strategic hiring to ensure that we can accomplish critical milestones.  We have identified potential candidates to fill a number of key positions, while outsourcing activities that benefit from economies of scale/expertise, including large-scale chemical synthesis, animal testing, clinical trial execution and regulatory affairs.  We have demonstrated the ability to leverage non-dilutive financing to meet critical early milestones, maintaining a semi-virtual structure and low burn rate.