Prospective Grant of Exclusive License: Treating and Preventing Inflammatory Bowel Disease (IBD) Involving Interleukin-13 (IL-13) and Natural Killer T (NKT) Cells, 19566 [E9-9856]

Agencies

• DEPARTMENT OF HEALTH AND HUMAN SERVICES
• National Institutes of Health

[Federal Register Volume 74, Number 81 (Wednesday, April 29, 2009)]
[Notices]
[Page 19566]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-9856]



[[Page 19566]]

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DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Prospective Grant of Exclusive License: Treating and Preventing 
Inflammatory Bowel Disease (IBD) Involving Interleukin-13 (IL-13) and 
Natural Killer T (NKT) Cells

AGENCY: National Institutes of Health, Public Health Service, HHS.

ACTION: Notice.

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SUMMARY: This is notice, in accordance with 35 U.S.C. 209(c)(1) and 37 
CFR Part 404.7(a)(1)(i), that the National Institutes of Health, 
Department of Health and Human Services, is contemplating the grant of 
an exclusive patent license to practice the inventions embodied in PCT 
Patent Application No. PCT/US02/18790, filed June 14, 2002, which 
published as WO 2004/001655 on December 31, 2003, now expired, entitled 
``Method of Treating and Preventing Colitis Involving IL-13 and NK-T 
Cells'' [HHS Ref. No. E-131-2002/0-PCT-01];U.S. Patent Application No. 
10/517,898, filed December 13, 2004, which was published as US-2006-
0024306 A1 on February 2, 2006, entitled ``A Method of Treating 
Inflammatory Bowel Disease (IBD)'' [HHS Ref. No. E-131-2002/0-US-02]; 
European Patent Application No. 02742057.9, filed June 14, 2002, which 
published as 1552462 on July 13, 2005, entitled ``Method of Treating 
and Preventing Colitis Involving IL-13 and NK-T Cells'' [HHS Ref. No. 
E-131-2002/0-EP-08]; Australian Patent Application No. 2002315115, 
filed June 14, 2002, entitled ``Method of Treating and Preventing 
Colitis Involving IL-13 and NK-T Cells'' [HHS Ref. No. E-131-2002/0-AU-
05]; Japanese Patent Application No. 2004515561, filed June 14, 2002, 
entitled ``Method of Treating and Preventing Colitis Involving IL-13 
and NK-T Cells'' [HHS Ref. No. E-131-2002/0-JP-04]; New Zealand Patent 
Application No. 537726, filed June 14, 2002, entitled ``Method of 
Treating and Preventing Colitis Involving IL-13 and NK-T Cells'' [HHS 
Ref. No. E-131-2002/0-NZ-06]; Hong Kong Patent Application No. 
05112119.6, filed June 14, 2002, entitled ``Method of Treating and 
Preventing Colitis Involving IL-13 and NK-T Cells'' [HHS Ref. No. E-
131-2002/0-HK-09]; South African Patent Application No. 2005/00375, 
filed June 14, 2002, entitled ``Method of Treating and Preventing 
Colitis Involving IL-13 and NK-T Cells'' [HHS Ref. No. E-131-2002/0-ZA-
07]; Canadian Patent Application No. 2489540, filed June 14, 2002, 
entitled ``Method of Treating and Preventing Colitis Involving IL-13 
and NK-T Cells'' [HHS Ref. No. E-131-2002/0-CA-03]; U.S. Provisional 
Patent Application No. 60/671,624, filed April 15, 2005, now abandoned, 
entitled ``Treatment and prevention of IBD using Mutant and Chimeric 
IL-13 Molecules'' [HHS Ref. No. E-003-2005/0-US-01]; PCT Patent 
Application No. PCT/US06/014393, filed April 14, 2006, now expired, 
entitled ``Methods of Treating and Preventing Inflammatory Bowel 
Disease Involving IL-13 and NKT Cells,'' which published as WO 2006/
113614 on October 20, 2006 [HHS Ref. No. E-003-2005/0-PCT-02]; European 
Patent Application No. 06750435.7, filed November 12, 2007, entitled 
``Methods of Treating and Preventing Inflammatory Bowel Disease 
Involving IL-13 and NKT Cells,'' which published as 1877074 on January 
16, 2008, [HHS Ref. No. E-003-2005/0-EP-04]; and U.S. Patent 
Application No. 11/918,711, filed April 14, 2006, entitled ``Treatment 
and Prevention of Inflammatory Bowel Disease (IBD) Using Mutant and 
Chimeric IL-13 Molecules'' [HHS Ref. No. E-003-2005/0-US-03] to Innate 
Immune, Inc. which has an office in Stanford, California, U.S.A. The 
patent rights in these inventions have been assigned to the United 
States of America and Brigham and Women's Hospital.
    The prospective exclusive license territory may be ``worldwide'', 
and the field of use may be limited to ``the use of agents that 
modulate Natural Killer T cell (NKT cell) activity and/or NKT cell 
number a) by interaction with antigen-presenting cells expressing CD1d 
family of proteins, and/or b) by interaction with NKT cell receptors 
that bind to antigen-presenting cells expressing CD1d family of 
proteins, as therapeutics for the treatment or prevention of 
inflammatory bowel disease (IBD), including ulcerative colitis and 
Crohn's disease.''

DATES: Only written comments and/or applications for a license which 
are received by the NIH Office of Technology Transfer on or before June 
29, 2009 will be considered.

ADDRESSES: Requests for copies of the patent application, inquiries, 
comments, and other materials relating to the contemplated exclusive 
license should be directed to: Suryanarayana (Sury) Vepa, Ph.D., J.D., 
Licensing and Patenting Manager, Office of Technology Transfer, 
National Institutes of Health, 6011 Executive Boulevard, Suite 325, 
Rockville, MD 20852-3804; Telephone: (301) 435-5020; Facsimile: (301) 
402-0220; E-mail: vepas@mail.nih.gov.

SUPPLEMENTARY INFORMATION: The subject technology is directed to 
methods of treating inflammatory bowel disease (IBD), more specifically 
Ulcerative Colitis (UC). The inventors of this technology have used a 
mouse model of experimental colitis (OC) to show that Interleukin (IL)-
13, a Th2 cytokine, is a significant pathologic factor in OC and that 
neutralizing IL-13 in these animals effectively prevents colitis 
(Immunity (2002) 17, 629-638). The subject technology provides for 
methods of treating UC by reducing NKT cell activity. This reduction in 
NKT cell activity can be accomplished by inhibition of the cytokine IL-
13 or its receptor, IL-13R, or through modulation of another NKT cell 
surface receptor, such as the T-cell receptor. The T-cell receptor is 
activated by the glycoprotein, CD1d, which is expressed on the surface 
of antigen-presenting cells.
    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 sixty 
(60) days from the date of this published notice, the 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.
    Applications for a license in the field of use filed in response to 
this notice will be treated as objections to the grant of the 
contemplated exclusive license. Comments and objections submitted 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.

    Dated: April 23, 2009.
Richard U. Rodriguez,
Director, Division of Technology Development and Transfer, Office of 
Technology Transfer, National Institutes of Health.
[FR Doc. E9-9856 Filed 4-28-09; 8:45 am]
BILLING CODE 4140-01-P