Posted: 2016-05-03 in Press Releases
Nexvet and Zenoaq Announce PD-1 mAb Candidate for Canine Cancer
USDA Regulatory Jurisdiction Confirmed
The research and development collaboration between Nexvet and Zenoaq is focused on PETizing mAbs identified by Zenoaq to create candidates in immuno-oncology and allergy/inflammation for companion animals. Nexvet and Zenoaq will share the development costs of their collaboration programs. Zenoaq will retain European and Asian marketing rights to any resulting products, with Nexvet retaining rights to the rest of the world, including
“Cancer therapeutics is an area where veterinary medicine has not benefited from the many major advances in human biologics development. Cancer leads to significant morbidity and mortality in pet dogs, and the incidence of cancer will only increase as dogs live longer. Given the wealth of data generated in humans supporting the attractive safety profile and efficacy of PD-1 inhibitors against a variety of tumor types, we are excited to be advancing an anti-PD-1 antibody program for dogs with Zenoaq,” said Dr.
“Nexvet’s PETization technology and expertise with veterinary mAb development have delivered the first key milestone for our collaboration. We are extremely pleased the starting anti-PD-1 mAbs first identified by Zenoaq’s collaborator, Professor
About PD-1 and canine cancer
The PD-1 protein and a partner molecule, programmed death-ligand 1 (PD-L1), act in concert to reduce the immune system’s anti-tumor activity, allowing cancer growth and spread. In human medicine, blocking the interactions of PD-1 and PD-L1 has resulted in approved therapies with attractive safety profiles that demonstrate efficacy against multiple tumor types. These advancements have led to immuno-oncology (also called cancer immunotherapy) being hailed as a breakthrough for oncology, and a major investment target. The first human PD-1 inhibitor received regulatory approval in late 2014, and PD-1 inhibitors alone are predicted to achieve human sales of approximately
Nexvet and Zenoaq believe the clinical successes seen in human disease can be replicated in canine disease to produce effective therapies for multiple tumor types in dogs. Successful cancer immunotherapies would be a new paradigm in veterinary oncology where current standards of care, including surgery, chemotherapy and radiotherapy, have exhibited significant treatment limitations.
Nexvet’s PETization platform is designed to build upon the safety and efficacy data from clinically tested human therapies to create new candidates for companion animals, thereby reducing clinical risk and development cost. Blocking canine PD-1/PD-L1 interactions has been shown to result in an increase of immune cell activity, via a similar mechanism to that observed in humans. In related research, high levels of PD-L1 expression were detected in a majority of tumor samples taken from several types of canine cancer, suggesting that PD-1/PD-L1 interactions may be exploited by the cancers.
Dogs are susceptible to many of the same types of cancers that afflict people. Epidemiological studies have indicated that cancer is the leading cause of death in dogs over 10 years of age, with 50 percent of older dogs developing cancer and approximately one in four dogs eventually dying from cancer.
* Conditional licensure allows for market entry of a product on a comparatively rapid basis, under certain conditions, after a demonstration of purity, safety and a reasonable expectation of efficacy. While a conditional licensure is in place, the license holder continues to develop efficacy data.
About Zenoaq (http://www.zenoaq.jp/english/)
Established in 1946, Zenoaq (
About Nexvet (www.nexvet.com)
Nexvet is a veterinary biologics developer focused on transforming the therapeutic market for companion animals, such as dogs and cats, by developing and commercializing novel, species-specific biologics. Nexvet’s proprietary PETization™ platform is designed to rapidly design monoclonal antibodies (mAbs) that are recognized as “self” or “native” by an animal’s immune system, a property Nexvet refers to as “100% species-specificity.” Nexvet’s product candidates also build upon the safety and efficacy data from clinically tested human therapies, thereby reducing clinical risk and development cost.
Nexvet is leveraging diverse global expertise and incentives to build a vertically integrated biopharmaceutical company, which conducts drug discovery in Australia, conducts clinical development in the United States and
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