This site displays a prototype of a “Web 2.0” version of the daily Federal Register. It is not an official legal edition of the Federal Register, and does not replace the official print version or the official electronic version on GPO’s govinfo.gov.
The documents posted on this site are XML renditions of published Federal Register documents. Each document posted on the site includes a link to the corresponding official PDF file on govinfo.gov. This prototype edition of the daily Federal Register on FederalRegister.gov will remain an unofficial informational resource until the Administrative Committee of the Federal Register (ACFR) issues a regulation granting it official legal status. For complete information about, and access to, our official publications and services, go to About the Federal Register on NARA's archives.gov.
The OFR/GPO partnership is committed to presenting accurate and reliable regulatory information on FederalRegister.gov with the objective of establishing the XML-based Federal Register as an ACFR-sanctioned publication in the future. While every effort has been made to ensure that the material on FederalRegister.gov is accurately displayed, consistent with the official SGML-based PDF version on govinfo.gov, those relying on it for legal research should verify their results against an official edition of the Federal Register. Until the ACFR grants it official status, the XML rendition of the daily Federal Register on FederalRegister.gov does not provide legal notice to the public or judicial notice to the courts.
National Institutes of Health, Public Health Service, HHS.
This is notice, in accordance with 35 U.S.C. 209(c)(1) and 37 CFR 404.7(a)(1)(i), that the National Institutes of Health (NIH), Department of Health and Human Services, is contemplating the grant of an exclusive license to practice the invention embodied in:
(1) U.S. Patent No. 6,387,662, issued May 14, 2002, entitled “Synthesis and Purification of Hepatitis C Virus-Like particles” (E-009-1997/0) (Inventors: T. Jake Liang and Thomas F. Baumert (NIDDK)). This application is a continuation of and claims the benefit of priority of International Application No. PCT/US97/05096 filed on March 25, 1997, which claims priority to U.S. patent application No. 60/030,238, filed November 8, 1996.
(2) PCT/US97/05096 filed March 25, 1997, entitled “Synthesis and Purification of Hepatitis C Virus-Like particles in vitro” (related to E-009-1997/0) (Inventors: T. Jake Liang and Thomas F. Baumert (NIDDK)), National Stage filed in Australia (Patent No. 738585, issued January 03, 2002), the European Union (European Patent Office Patent Application Number 9791652.6), Canada (Patent Application Number 2269097), and in Japan (Patent Application Number 10-522521).
to Virionics Corporation, having a place of business in Odenton, Maryland. The patent rights in this invention have been assigned to the United States of America.
Only written comments and/or application for a license which are received by the NIH Office of Technology Transfer on or before September 8, 2003 will be considered.
Requests for a copy of the patent application, inquiries, comments and other materials relating to the contemplated license should be directed to: Peter Soukas, Office of Technology Transfer, National Institutes of Health, 6011 Executive Boulevard, Suite 325, Rockville, MD 20852-3804; E-mail: email@example.com; Telephone: (301) 435-4646; Facsimile: (301) 402-0220.End Preamble Start Supplemental Information
The technology relates to production of Start Printed Page 41167enveloped RNA virus-like particles in vitro in insect cells using a recombinant baculovirus vector containing a cDNA coding for viral structural proteins. In vitro production and purification of hepatitis C virus (HCV)-like particles containing HCV core protein, E1 protein and E2 protein is described. Sucrose gradient purified HCV-like particles exhibited similar biophysical properties as putative HCV virions. Mice injected with HCV-like particles developed HCV-specific antibodies indicating that the particles are immunogenic. HCV-like particles, purified in large quantities, may be useful in HCV vaccine development or in diagnostic kits.
The prospective exclusive license will be royalty bearing and will comply with the terms and conditions of 35 U.S.C. 209 and 37 CFR 404.7. The prospective exclusive license may be granted unless, within 60 days from the date of this published Notice, NIH receives written evidence and argument that establishes that the grant of the license would not be consistent with the requirements of 35 U.S.C. 209 and 37 CFR 404.7.
The field of use may be limited to vaccine products for prevention and treatment of chronic hepatitis C (HCV) infections.
Properly filed competing applications for a license filed in response to this notice will be treated as objections to the contemplated license. Comments and objections submitted in response to this notice will not be made available for public inspection, and, to the extent permitted by law, will not be released under the Freedom of Information Act, 5 U.S.C. 552.Start Signature
Dated: July 2, 2003.
Steven M. Ferguson,
Acting Director, Division of Technology Development and Transfer, Office of Technology Transfer.
[FR Doc. 03-17405 Filed 7-9-03; 8:45 am]
BILLING CODE 4140-01-P