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62 FR (04/21/1997) » 97-10201. Availability of Non-Exclusive, Exclusive, or Partially Exclusive Licensing of U.S. Patent Application Concerning Recombinant F1-V Plague Vaccine
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