Single Administration of GenVec's Vaccine Provides Protective Immunity Against  HSV in Pre-clinical Animal Models 
  GAITHERSBURG, Md., Dec. 17, 2012 /PRNewswire via COMTEX/ -- GenVec, Inc. (GNVC)  announced today that data were presented on its HSV vaccine program at the  Keystone Symposia meeting on Immunological Mechanisms of Vaccination, which is  taking place in Ottawa, Ontario from December 13 to December 18, 2012. 
  The company disclosed that a single administration of its genetic vaccine was  effective against HSV2 in two industry-accepted HSV disease models. Specifically,  immunization was shown to reduce viral shedding, and the recurrence and severity  of lesions. 
  GenVec's HSV vaccine candidate generated effective immune responses in animal  models; and is composed of two novel antigens, as well as a proprietary,  non-human adenoviral vector. 
  "We have substantial evidence that HSV infection can be controlled by inducing an  appropriate T-cell response," said Dr. Lisa Wei, Senior Director of Research and  head of GenVec's HSV program. "The data presented at this symposium demonstrate  the progress we are making towards the goal of creating a vaccine for treatment  and potentially prophylaxis of HSV infection." 
  Research reported in this release was supported by the National Institute of  Allergy and Infectious Diseases of the National Institutes of Health under grant  number 5R43AIO77147-02. The content is solely the responsibility of the authors  and does not necessarily represent the official views of the National Institutes  of Health. 
  About Herpes Simplex Virus (HSV) 
  In the United States, approximately 40 million people are currently infected with  HSV2, which is responsible for most cases of genital herpes, and 1.6 million new  infections occur each year. About 25% of those infected with the virus suffer  clinical symptoms. Even higher infection rates are evident in developing  countries. HSV2 infection is associated with increased HIV infection and  transmission; and further complications of HSV are also often seen in those  co-infected with HIV. HSV infections are permanent, and result in periodic virus  shedding. Although antiviral regimens have become a standard of care, their  inconvenience, cumulative cost and potential for drug resistance further  underscore the need for safe, new approaches to reduce HSV lesions, virus  shedding, and transmission. Estimated costs of treating HSV in the United States  alone are close to $1 billion, primarily for drugs and outpatient medical care.  There is no FDA-approved vaccine for HSV. 
  About GenVec 
  GenVec is a biopharmaceutical company using differentiated, proprietary  technologies to create superior therapeutics and vaccines. A key component of our  strategy is to develop and commercialize our product candidates through  collaborations. GenVec is working with leading companies and organizations such  as Novartis, Merial, and the U.S. Government to support a portfolio of product  programs that address the prevention and treatment of a number of significant  human and animal health concerns. GenVec's development programs address  therapeutic areas such as hearing loss and balance disorders; as well as vaccines  against infectious diseases including respiratory syncytial virus (RSV), herpes  simplex virus (HSV), dengue fever, malaria, and human immunodeficiency virus  (HIV). In the area of animal health we are developing vaccines against  foot-and-mouth disease (FMD). Additional information about GenVec is available at  genvec.com and in the Company's filings with the U.S. Securities and  Exchange Commission. 
  Statements herein relating to future financial or business performance,  conditions or strategies and other financial and business matters, including  expectations regarding funding, grants, collaborations, revenues, cash burn  rates, the development of products and the success of the Company's  collaborations, including with Novartis and Merial, are forward-looking  statements within the meaning of the Private Securities Litigation Reform Act.  GenVec cautions that these forward-looking statements are subject to numerous  assumptions, risks and uncertainties, which change over time. Factors that may  cause actual results to differ materially from the results discussed in the  forward-looking statements or historical experience include risks and  uncertainties, including the failure by GenVec to secure and maintain  relationships with collaborators; risks relating to the early stage of GenVec's  product candidates under development; uncertainties relating to research and  development activities; risks relating to the commercialization, if any, of  GenVec's proposed product candidates; dependence on the efforts of collaborators  and third parties; dependence on intellectual property; currently unanticipated  expenses, and risks that we may lack the financial resources and access to  capital to fund our operations. Further information on the factors and risks that  could affect GenVec's business, financial conditions and results of operations,  are contained in GenVec's filings with the U.S. Securities and Exchange  Commission (SEC), which are available at sec.gov. These  forward-looking statements speak only as of the date of this press release, and  GenVec assumes no duty to update forward-looking statements.  Retail Investor and Media Contact Institutional Investor Contact  GenVec, Inc.S.A. Noonan Communications  Douglas J. SwirskySusan A. Noonan  (240) 632-5510(212) 966-3650  dswirsky@genvec.comsusan@sanoonan.com  |