PsiOxus Therapeutics to present promising new data on novel oncolytic immunoncology platform at AACR 2015
OXFORD, UK – 16 April 2015
PsiOxus Therapeutics Ltd. (PsiOxus), an oncolytic immunoncology company, has announced that it will present data highlighting the progress of its next generation “Antibody Armed EnAd” (AbEnAd) anti-cancer therapeutic platform at the American Association for Cancer Research (AACR) Annual Meeting 2015 in Philadelphia, PA April 19-22, 2015. AbEnAd is the antibody armed series from the “Armed EnAd Platform” which is based upon the company’s flagship therapeutic oncolytic virus, enadenotucirev (EnAd). EnAd was developed using the principles of natural selection to specifically target and destroy cancer cells, and to allow systemic intravenous delivery.
Brian Champion, Head of PsiOxus R&D, commented: “We have previously demonstrated that EnAd can be delivered intravenously. The possibility to ‘arm’ the EnAd particles with specific anti-cancer therapeutic agents, now enables the production of high concentrations of immunotherapeutics, such as checkpoint inhibitor antibodies, and other therapeutic agents selectively within the tumour microenvironment where they are needed. The ability to use systemic administration means that armed EnAd particles can reach and express their therapeutic payloads in both the primary tumour as well as its metastases. The ability to “arm” the virus with different therapeutic agents, now opens the path for this exciting new technology to target a wide variety of cancers.”
Forcing Cancer Cells to Produce Anti-Tumour Drugs
In the AbEnAd platform, EnAd viral particles are ‘armed’ with the genetic instructions required to produce a specific therapeutic anti-cancer antibody. Once the AbEnAd particles infect a cancer cell, it directs the machinery of the host cell to produce new copies of the virus as well as the specific anti-cancer antibody it is carrying – and this antibody is then able to exert its action on surrounding cancer cells or other local components of the tumour, such as cells of the immune system.
Because this process has an amplification effect, the AbEnAd viral particles can then go on to infect neighbouring cells, releasing more of the anti-cancer antibody “payload” in an expanding radius to impact surrounding tumour cells. The virus infection also triggers the release of inflammatory mediators that serve to attract and stimulate immune cells, such as cytotoxic T-cells that can induce tumour cell death.. The antibody payloads encoded in the virus can thus be designed to facilitate these anti-cancer effects.
The PsiOxus team is currently working with a class of therapeutic antibodies that inhibit immune checkpoint pathways, which have been shown to be very effective against a range of different cancer types in a number of previous external studies.
However, besides antibodies of different specificities in the AbEnAd series, the “Armed EnAd Platform” can include a broad variety of agents for the “arming”, such as inhibitory or stimulatory molecules that may be proteins/peptides or nucleotide based such as RNAi. This allows targeting of otherwise “undrugable” pathways as well as the use of agents that cannot feasibly be delivered systemically due to their general side effects, e.g. immune-stimulatory molecules.
Professor Len Seymour, Professor of Gene Therapies, Department of Oncology, University of Oxford, and member of the PsiOxus Scientific Advisory Board, commented: ‘The “Armed EnAd Platform” development should be game-changing for anti-cancer biologics. Not only can we target and destroy cancer cells specifically using the EnAd virus, we now see it is possible to force the cancer cell to produce and secrete anti-cancer biologics which can augment the local anticancer effect. This targeted-expression approach maximises the level of the biologic at the tumour site and simultaneously minimises unwanted systemic exposure, giving a far better therapeutic index than could be previously achieved. What is most exciting from a scientific standpoint, is the versatility of the “Armed EnAd Platform” in terms of the variety of payloads that can be encoded. This platform provides a significant step forward in the search for new ways to treat cancer, in particular for challenging cancer subtypes that do not yield to conventional therapies.’
Learn more at AACR 2015
The most recent results from the ongoing AbEnAd research programme will be presented as part of a poster session at the AACR meeting on Sunday 19 April 2015 from 13:00 to 17:00 (abstract number 295). For more information on AbEnAd and the EnAd arming platform, please visit www.psioxus.com.
PsiOxus also recently announced the expansion of its first generation EnAd clinical programme, following success with tumour-specific delivery through intravenous administration. Full details can be found on the PsiOxus website.