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GenVec Reports Fourth Quarter And 2012 Year-End Financial Results
Date:3/22/2013

Protective Immune Responses" was published online in PloS ONE.

Animal Health

  • The Company's foot-and-mouth disease (FMD) vaccine for use in cattle received a conditional license from the U.S. Department of Agriculture's Animal and Plant Health Inspection Service (APHIS), which provides that the product may be distributed as authorized by Federal emergency management officials within USDA, should the need for the product arise.  This is GenVec's first approved product and also the first FMD vaccine licensed by the USDA Center for Veterinary Biologics. 
  • 2012 Financial ResultsRevenue decreased 47% to $9.4 million in 2012 from $17.7 million in 2011.  The decrease in 2012 is primarily due to decreased revenue of $5.6 million, $1.5 million, and $1.2 million generated by our hearing loss and balance disorders, HIV, and foot and mouth disease programs, respectively, over the prior year.  We entered into a collaboration agreement with Novartis in January 2010, which accounted for $0.9 million and $3.8 million of revenue in 2012 and 2011, respectively, and a development agreement related to the supply of clinical trial material related to activities under the collaboration agreement in August 2010, which accounted for $3.5 million and $6.0 million in revenue in 2012 and 2011, respectively.  A reduced work scope as we near completion of our development work under the two Novartis agreements resulted in decreased revenue in 2012 as compared to 2011.  Decreased revenue associated with our foot and mouth disease program is due mainly to a decrease in work scope and the successful completion of field safety studies under our agreements with the Department of Homeland Security (DHS).  Decreased revenue associated with our HIV program as compared to the prior year is due to reduced work scope.

    Operating expenses for 2012 decreased 7% to $23.5 million from $25.2 million in 2011.  Research and development expense
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