AmpliPhi BioSciences Corporation (OTC:APHB) (“AmpliPhi”) the leader in the discovery and development of bacteriophage-based therapies to treat drug resistant bacterial infections announced today a Collaborative Research and Development Agreement (CRADA) with the United States Army Medical Research and Materiel Command (USAMRMC) and the Walter Reed Army Institute of Research (WRAIR).
The CRADA will focus on developing and commercializing bacteriophage therapeutics to treat Staphylococcus aureus Escherichia coli and Pseudomonas aeruginosa infections. The increasing prevalence of antibiotic-resistant bacteria poses a serious threat to public health and military personnel and is a major problem in hospitals and clinics around the world. The initial indication will be wounds and skin infections from S aureus which is the leading pathogen in healthcare-associated infections in the United States as a whole accounting for 30.4% of surgical site infections.
AmpliPhi will retain global regulatory ownership and commercial rights to all products developed as a result of the agreement. USAMRMC will gain access rights to any products developed. WRAIR will be responsible for cGMP production of the lead Staphylococcus product AmpliPhage-002 for Phase 1 and 2 clinical trials at its Bioproduction Facility. Further details of the agreement including financial terms were not disclosed.
Philip J. Young CEO of AmpliPhi said: “This collaboration is a significant partnership for our company. It combines AmpliPhi’s expertise in the discovery and development of bacteriophage-based therapies with the US Army’s scientific and clinical research for the development of phage therapies for treatment of bacterial infections. It will serve to expedite the development testing and approval of new treatment modalities. Working together I believe we will be able to improve the care of patients with these serious often life threatening infections.”
Dr Kenneth A. Bertram Principle Assistant for Acquisition at USAMRMC said: “Multidrug resistant bacterial infections are a significant challenge for US military as they are for the rest of the world. The Army has had a long standing interest in the potential of innovative therapies to address this challenge. This bacteriophage collaboration is an important step in the battle to find much needed alternative therapies to treat these infections.”
If initial development activities are successful the scope of the collaboration could expand to research and developbacteriophage therapies against other diseases of mutual interest.
About AmpliPhi BioSciences
AmpliPhi BioSciences Corporation [OTCBB:APHB] is a biotechnology company focused on the development and commercialization of novel bacteriophage-based therapeutics for human and animal applications. The Company’s product development programs are targeting Gram-negative infections that are often resistant to existing antibiotic treatments. AmpliPhi was created in 2011 through the merger of BioControl Ltd with Targeted Genetics Inc. and subsequent combination with Special Phage Services in 2012. The Company is US-headquartered in Richmond Virginia and has operations in Colworth UK and Sydney Australia. For more information visit www.ampliphibio.com
Bacteriophages are naturally occurring viruses that are highly specific for the bacterial hosts they infect. They can rapidly kill their host amplifying themselves in the process. Bacteriophages are unaffected by antibiotic resistance and are able to disrupt bacterial biofilms. Such biofilms are a major line of defence for bacteria contributing to antibiotic resistance. Bacteriophages are able to penetrate biofilms and replicate locally to high levels to produce strong local therapeutic effects.
Forward Looking Statements
Statements in this press release about the potential use of bacteriophages to treat bacterial infections and the development of bacteriophage-based therapies are forward looking statements subject to risks and uncertainties including without limitation the risk that such therapies may not be successfully developed will require extensive and expensive pre-clinical and clinical testing may not be safe or efficacious and may not be approved for marketing by the United States Food and Drug Administration or any foreign regulatory agency.Business Wire
Last updated on: 01/07/2013
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