97-10201. Availability of Non-Exclusive, Exclusive, or Partially Exclusive Licensing of U.S. Patent Application Concerning Recombinant F1-V Plague Vaccine  

  • [Federal Register Volume 62, Number 76 (Monday, April 21, 1997)]
    [Notices]
    [Page 19314]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 97-10201]
    
    
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    DEPARTMENT OF DEFENSE
    
    Department of the Army
    
    
    Availability of Non-Exclusive, Exclusive, or Partially Exclusive 
    Licensing of U.S. Patent Application Concerning Recombinant F1-V Plague 
    Vaccine
    
    AGENCY: U.S. Army Medical Research and Materiel Command, DOD.
    
    ACTION: Notice.
    
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    SUMMARY: In accordance with 38 CFR 404.6, announcement is made of the 
    availability of U.S. Patent Application SN 08/699,716 entitled 
    ``Recombinant F1-V Plague Vaccine,'' filed December 18, 1996. This 
    patent has been assigned to the United States Government as represented 
    by the Secretary of the Army.
    
    ADDRESSES: Commander, U.S. Army Medical Research and Materiel Command, 
    Command Judge Advocate, ATTN: MCMR-JA, 504 Scott Street, Fort Detrick, 
    MD 21702-5012.
    
    FOR FURTHER INFORMATION CONTACT: Mr. John F. Moran, Patent Attorney, 
    301-619-7807, Fax 301-619-5034.
    
    SUPPLEMENTARY INFORMATION: A recombinant plague vaccine (F1-V) based on 
    a fusion protein composed of the entire capsule protein (F1) and V 
    protein of Yersinia pestis has been developed. Initial preclinical 
    studies in mice have shown this fusion protein when combined with an 
    adjuvant to be efficicacious against fully virulent wild-type and F-1 
    strains of Yersinia pestis. The vaccine has been tested against both 
    subcutaneous and aerosol challenges, which should mimic the bubonic and 
    pneumonic form of plague. This F1-V vaccine has been shown to be 
    superior to the licensed, whole cell, Plague Vaccine USP in a mouse 
    model. It also offers the advantage of being a defined product which 
    may be less reactogenic than the poorly defined whole cell vaccine. The 
    use of fusion protein offfers advantages of producing and purifying a 
    single protein, instead of two separate components, which may result in 
    lower manufacturing costs.
    Gregory D. Showalter,
    Army Federal Register Liaison Officer.
    [FR Doc. 97-10201 Filed 4-18-97; 8:45 am]
    BILLING CODE 3710-08-M
    
    
    

Document Information

Published:
04/21/1997
Department:
Army Department
Entry Type:
Notice
Action:
Notice.
Document Number:
97-10201
Pages:
19314-19314 (1 pages)
PDF File:
97-10201.pdf