Prospective Grant of an Exclusive License: “Vasostatin as Marrow Protectant” and “Use of Calreticulin and Calreticulin Fragments To Inhibit Endothelial Cell Growth and Angiogenesis and Suppress Tumor Growth”, 5351 [E6-1389]

Download as PDF Federal Register / Vol. 71, No. 21 / Wednesday, February 1, 2006 / Notices cchase on PROD1PC60 with NOTICES Scientific Review, National Institutes of Health, 6701 Rockledge Drive, Room 3192, MSC 7848, Bethesda, MD 20892, 301–435– 2309, pluded@csr.nih.gov. Name of Committee: Respiratory Sciences Integrated Review Group, Lung Cellular, Molecular, and Immunobiology Study Section. Date: February 22–23, 2006. Time: 8 a.m. to 6 p.m. Agenda: To review and evaluate grant applications. Place: Wyndham City Center Hotel, 1143 New Hampshire Ave., NW., Washington, DC 20037. Contact Person: George M. Barnas, PhD., Scientific Review Administrator, Center for Scientific Review, National Institutes of Health, 6701 Rockledge Drive, Room 2180, MSC 7818, Bethesda, MD 20892, 301–435– 0696, barnasg@csr.nih.gov. Name of Committee: Oncological Sciences Integrated Review Group, Chemo/Dietary Prevention Study Section. Date: February 22–24, 2006. Time: 5 p.m. to 5 p.m. Agenda: To review and evaluate grant applications. Place: Latham Hotel, 3000 M Street, NW., Washington, DC 20007. Contact Person: Sally A. Mulhern, PhD., Scientific Review Administrator, Center for Scientific Review, National Institutes of Health, 6701 Rockledge Drive, Room 6198, MSC 7804, Bethesda, MD 20892, (301) 435– 5877, mulherns@csr.nih.gov. Name of Committee: Brain Disorders and Clinical Neuroscience Integrated Review Group, Neural Basis of Psychopathology, Addictions and Sleep Disorders Study Section. Date: February 22–24, 2006. Time: 6 p.m. to 2 p.m. Agenda: To review and evaluate grant applications. Place: St. Gregory Hotel, 2033 M Street, NW., Washington, DC 20036. Contact Person: Julius Cinque, MS., Scientific Review Administrator, Center for Scientific Review, National Institutes of Health, 6701 Rockledge Drive, Room 5186, MSC 7846, Bethesda, MD 20892, (301) 435– 1252, cinquej@csr.nih.gov. (Catalogue of Federal Domestic Assistance Program Nos. 93.306, Comparative Medicine; 93.333, Clinical Research, 93.306, 93.333, 93.337, 93.393–93.396, 93.837–93.844, 93.846–93.878, 93.892, 93.893, National Institutes of Health, HHS.) Dated: January 24, 2006. Anna Snouffer, Acting Director, Office of Federal Advisory Committee Policy. [FR Doc. 06–919 Filed 1–31–06; 8:45 am] BILLING CODE 4140–01–M VerDate Aug<31>2005 17:49 Jan 31, 2006 Jkt 208001 DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Prospective Grant of an Exclusive License: ‘‘Vasostatin as Marrow Protectant’’ and ‘‘Use of Calreticulin and Calreticulin Fragments To Inhibit Endothelial Cell Growth and Angiogenesis and Suppress Tumor Growth’’ National Institutes of Health, Public Health Service, HHS. ACTION: Notice. AGENCY: SUMMARY: This notice, in accordance with 35 U.S.C. 209(c)(1) and 37 CFR 404.7(a)(1) (i), announces that the Department of Health and Human Services is contemplating the grant of an exclusive license to practice the inventions embodied in U.S. Patent No. 6,596,690 B2 entitled ‘‘Vasostatin as Marrow Protectant’’ (HHS Reference E– 230–2000/0); U.S. Patent Application No. 09/807,148 filed April 5, 2001, entitled ‘‘Use of Calreticulin and Calreticulin Fragments To Inhibit Endothelial Cell Growth and Angiogenesis and Suppress Tumor Growth’’ (HHS Reference E–082–1998/ 0–US–03); PCT Application No. PCT/ US99/23240 filed October 5, 1999 entitled ‘‘Use of Calreticulin and Calreticulin Fragments To Inhibit Endothelial Cell Growth and Angiogenesis and Suppress Tumor Growth’’ (HHS Reference E–082–1998/ 0–PCT–02); to RxKinetix, Inc. The patent rights in these inventions have been assigned to the United States of America. The prospective exclusive license territory may be worldwide and the field of use may be limited to development and sale of a pharmaceutical product useful in protecting bone marrow stem cells from the toxic effects of chemotherapy and radiotherapy. DATES: Only written comments and/or license applications which are received by the National Institutes of Health on or before April 3, 2006 will be considered. ADDRESSES: Requests for copies of the patent and/or patent applications, inquiries, comments and other materials relating to the contemplated exclusive license should be directed to: Mojdeh Bahar, J.D., Technology Licensing Specialist, Office of Technology Transfer, National Institutes of Health, 6011 Executive Boulevard, Suite 325, Rockville, MD 20852–3804. Telephone: (301) 435–2950; Facsimile: (301) 402– 0220; E-mail: baharm@od.nih.gov. PO 00000 Frm 00120 Fmt 4703 Sfmt 4703 5351 The technology claimed in the aforementioned patents is based on the discovery of the calreticulin N-domain (vasostatin) and the three previously uncharacterized properties of calreticulin. First, calreticulin N-domain is shown to stimulate the proliferation and survival in vitro of hematopoietic cells in the presence of previously identified growth factors. Second, Vasostatin is shown to protect hematopoietic cells in vitro from toxicity induced by a variety of chemotherapeutic agents. Third, Vasostatin is shown to protect a subject from toxicity to the hematopoietic system induced by chemotherapy or irradiation. 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 establish 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. This is a modification to the notice published in 70 FR 96, January 3, 2005. SUPPLEMENTARY INFORMATION: Dated: January 23, 2006. Steven M. Ferguson, Director, Division of Technology Development and Transfer, Office of Technology Transfer, National Institutes of Health. [FR Doc. E6–1389 Filed 1–31–06; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HOMELAND SECURITY Office of the Secretary [Docket No. DHS–2005–0057] Software Assurance Program: Building Better Quality and More Secure Software National Cyber Security Division, DHS. ACTION: Notice of availability. AGENCY: SUMMARY: The purpose of this notice is to inform the public and interested E:\FR\FM\01FEN1.SGM 01FEN1

Agencies

[Federal Register Volume 71, Number 21 (Wednesday, February 1, 2006)]
[Notices]
[Page 5351]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-1389]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Prospective Grant of an Exclusive License: ``Vasostatin as Marrow 
Protectant'' and ``Use of Calreticulin and Calreticulin Fragments To 
Inhibit Endothelial Cell Growth and Angiogenesis and Suppress Tumor 
Growth''

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

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: This notice, in accordance with 35 U.S.C. 209(c)(1) and 37 CFR 
404.7(a)(1) (i), announces that the Department of Health and Human 
Services is contemplating the grant of an exclusive license to practice 
the inventions embodied in U.S. Patent No. 6,596,690 B2 entitled 
``Vasostatin as Marrow Protectant'' (HHS Reference E-230-2000/0); U.S. 
Patent Application No. 09/807,148 filed April 5, 2001, entitled ``Use 
of Calreticulin and Calreticulin Fragments To Inhibit Endothelial Cell 
Growth and Angiogenesis and Suppress Tumor Growth'' (HHS Reference E-
082-1998/0-US-03); PCT Application No. PCT/US99/23240 filed October 5, 
1999 entitled ``Use of Calreticulin and Calreticulin Fragments To 
Inhibit Endothelial Cell Growth and Angiogenesis and Suppress Tumor 
Growth'' (HHS Reference E-082-1998/0-PCT-02); to RxKinetix, Inc. The 
patent rights in these inventions have been assigned to the United 
States of America.
    The prospective exclusive license territory may be worldwide and 
the field of use may be limited to development and sale of a 
pharmaceutical product useful in protecting bone marrow stem cells from 
the toxic effects of chemotherapy and radiotherapy.

DATES: Only written comments and/or license applications which are 
received by the National Institutes of Health on or before April 3, 
2006 will be considered.

ADDRESSES: Requests for copies of the patent and/or patent 
applications, inquiries, comments and other materials relating to the 
contemplated exclusive license should be directed to: Mojdeh Bahar, 
J.D., Technology Licensing Specialist, Office of Technology Transfer, 
National Institutes of Health, 6011 Executive Boulevard, Suite 325, 
Rockville, MD 20852-3804. Telephone: (301) 435-2950; Facsimile: (301) 
402-0220; E-mail: baharm@od.nih.gov.

SUPPLEMENTARY INFORMATION: The technology claimed in the aforementioned 
patents is based on the discovery of the calreticulin N-domain 
(vasostatin) and the three previously uncharacterized properties of 
calreticulin. First, calreticulin N-domain is shown to stimulate the 
proliferation and survival in vitro of hematopoietic cells in the 
presence of previously identified growth factors. Second, Vasostatin is 
shown to protect hematopoietic cells in vitro from toxicity induced by 
a variety of chemotherapeutic agents. Third, Vasostatin is shown to 
protect a subject from toxicity to the hematopoietic system induced by 
chemotherapy or irradiation.
    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 establish 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.
    This is a modification to the notice published in 70 FR 96, January 
3, 2005.

    Dated: January 23, 2006.
Steven M. Ferguson,
Director, Division of Technology Development and Transfer, Office of 
Technology Transfer, National Institutes of Health.
[FR Doc. E6-1389 Filed 1-31-06; 8:45 am]
BILLING CODE 4140-01-P
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.