Public Teleconference Regarding Licensing and Collaborative Research Opportunities for: Methods and Compositions Relating to Detecting Dihydropyrimidine Dehydrogenase (DPD), 38233 [E8-15182]

Download as PDF Federal Register / Vol. 73, No. 129 / Thursday, July 3, 2008 / Notices analysis. Please contact Dr. Robert Lipsky at 301/402–5591 or rlipsky@mail.nih.gov for more information. Dated: June 26, 2008. Richard U. Rodriguez, Director, Division of Technology Development and Transfer, Office of Technology Transfer, National Institutes of Health. [FR Doc. E8–15201 Filed 7–2–08; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Public Teleconference Regarding Licensing and Collaborative Research Opportunities for: Methods and Compositions Relating to Detecting Dihydropyrimidine Dehydrogenase (DPD) National Institutes of Health, Public Health Service, HHS. ACTION: Notice. AGENCY: mstockstill on PROD1PC66 with NOTICES Technology Summary This technology relates to a method of detecting DPD Splicing Mutations. Technology Description Scientists at the National Cancer Institute have discovered a method detecting DPD Splicing Mutations. This method can identify patients with such mutations, and thereby alert the health care provider that the patient will have an adverse reaction to the chemotherapeutic agent, 5–Fluorouracil. The invention relates to methods and compositions that are useful for detecting deficiencies in DPD levels in mammals including humans. Cancer patients having a DPD deficiency are at risk of a severe toxic reaction to the commonly used anticancer agent 5fluorouracil (5–FU). The technology encompasses DPD genes from human and pig, methods for detecting the level of nucleic acids that encode DPD in a patient, and nucleic acids that are useful as probes for this purpose. Novel applications of the methods include: • Screening of patients prior to the administration of the chemotherapeutic agent, 5–Fluorouracil. • Diminishing and potentially eliminating the severe side effects of 5– Fluorauracil in patients. Competitive Advantage of Our Technology 5–Fluorouracil (5–FU) is a therapeutic for the treatment of multiple cancers, including breast and colon cancers. In VerDate Aug<31>2005 16:46 Jul 02, 2008 Jkt 214001 the United States, approximately 275,000 cancer patients receive 5–FU annually. It is estimated that three percent (3%) of those patients develop some degree of toxic reaction. Patients suffering toxic reactions are difficult and expensive to treat further. Approximately, 15% of those developing toxic reaction, will die as a result of exposure to 5–FU. Death is typically caused by cardiotoxicity. More than 1,300 patients in the United States die each year as a result of 5–FU toxicity. These deaths are all potentially avoidable if patients that are likely to get adverse reaction with 5–FU treatment are detected prior to treatment. Patent Estate This technology consists of the following patents and patent applications: I. United States Patent Number 5,856,454 entitled ‘‘cDNA for Human and Pig Dihydropyrimidine Dehydrogenase,’’ issued January 5, 1999 (HHS Ref. No. E–157–1994/0–US–01); II. United States Patent Number 6,015,673 entitled ‘‘Cloning and Expression of cDNA for Human Dihydropyrimidine Dehydrogenase,’’ issued January 18, 2000 (HHS Ref. No. E–157–1994/0–US–03); III. United States Patent Number 6,787,306 entitled ‘‘Methods and Compositions for Detecting Dihydropyrimidine Dehydrogenase Splicing Mutations,’’ issued September 7, 2004 (HHS Ref. No. E–157–1994/1– US–01); IV. United States Pre-Grant Publication number 2005/0136433A1 corresponding to application serial number 10/911237 entitled ‘‘Methods and Compositions for Detecting Dihydropyrimidine Dehydrogenase Splicing Mutations,’’ published June 23, 2005 (HHS Ref. No. E–157–1994/1–US– 19) and all issued and pending counterparts in Europe, Canada, and Australia. Next Step: Teleconference There will be a teleconference where the principal investigator will explain this technology. Licensing and collaborative research opportunities will also be discussed. If you are interested in participating in this teleconference please call or e-mail Mojdeh Bahar; (301) 435–2950; baharm@mail.nih.gov. OTT will then e-mail you the date, time and number for the teleconference. PO 00000 Frm 00062 Fmt 4703 Sfmt 4703 38233 Dated: June 26, 2008. Richard U. Rodriguez, Director, Division of Technology Development and Transfer, Office of Technology Transfer. National Institutes of Health. [FR Doc. E8–15182 Filed 7–2–08; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Institute on Alcohol Abuse and Alcoholism; Notice of Closed Meeting Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. Appendix 2), notice is hereby given of the following meeting. The meeting will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: National Institute on Alcohol Abuse and Alcoholism Special Emphasis Panel; Deferred AA3 Applications. Date: July 16, 2008. Time: 1 to 3 p.m. Agenda: To review and evaluate grant applications. Place: National Institutes of Health, 5635 Fishers Lane, Room 3042, Rockville, MD 20852 (Telephone Conference Call). Contact Person: Katrina L. Foster, PhD, Scientific Review Officer, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, 5635 Fishers Lane, Room 3042, Rockville, MD 20852, 301–443–4032, katrina@mail.nih.gov. The applications being reviewed in EEO2 were initially assigned to panel AA3. The appropriate expertise was not available in AA3; thus, these applications were removed and are being reviewed in a SEP meeting. (Catalogue of Federal Domestic Assistance Program Nos. 93.271, Alcohol Research Career Development Awards for Scientists and Clinicians; 93.272, Alcohol National Research Service Awards for Research Training; 93.273, Alcohol Research Programs; 93.891, Alcohol Research Center Grants, National Institutes of Health, HHS) Dated: June 25, 2008. Jennifer Spaeth, Director, Office of Federal Advisory Committee Policy. [FR Doc. E8–14924 Filed 7–2–08; 8:45 am] BILLING CODE 4140–01–M E:\FR\FM\03JYN1.SGM 03JYN1

Agencies

[Federal Register Volume 73, Number 129 (Thursday, July 3, 2008)]
[Notices]
[Page 38233]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-15182]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Public Teleconference Regarding Licensing and Collaborative 
Research Opportunities for: Methods and Compositions Relating to 
Detecting Dihydropyrimidine Dehydrogenase (DPD)

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

ACTION: Notice.

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

Technology Summary

    This technology relates to a method of detecting DPD Splicing 
Mutations.

Technology Description

    Scientists at the National Cancer Institute have discovered a 
method detecting DPD Splicing Mutations. This method can identify 
patients with such mutations, and thereby alert the health care 
provider that the patient will have an adverse reaction to the 
chemotherapeutic agent, 5-Fluorouracil.
    The invention relates to methods and compositions that are useful 
for detecting deficiencies in DPD levels in mammals including humans. 
Cancer patients having a DPD deficiency are at risk of a severe toxic 
reaction to the commonly used anticancer agent 5-fluorouracil (5-FU). 
The technology encompasses DPD genes from human and pig, methods for 
detecting the level of nucleic acids that encode DPD in a patient, and 
nucleic acids that are useful as probes for this purpose.
    Novel applications of the methods include:
     Screening of patients prior to the administration of the 
chemotherapeutic agent, 5-Fluorouracil.
     Diminishing and potentially eliminating the severe side 
effects of 5-Fluorauracil in patients.

Competitive Advantage of Our Technology

    5-Fluorouracil (5-FU) is a therapeutic for the treatment of 
multiple cancers, including breast and colon cancers. In the United 
States, approximately 275,000 cancer patients receive 5-FU annually. It 
is estimated that three percent (3%) of those patients develop some 
degree of toxic reaction. Patients suffering toxic reactions are 
difficult and expensive to treat further. Approximately, 15% of those 
developing toxic reaction, will die as a result of exposure to 5-FU. 
Death is typically caused by cardiotoxicity. More than 1,300 patients 
in the United States die each year as a result of 5-FU toxicity. These 
deaths are all potentially avoidable if patients that are likely to get 
adverse reaction with 5-FU treatment are detected prior to treatment.

Patent Estate

    This technology consists of the following patents and patent 
applications:
    I. United States Patent Number 5,856,454 entitled ``cDNA for Human 
and Pig Dihydropyrimidine Dehydrogenase,'' issued January 5, 1999 (HHS 
Ref. No. E-157-1994/0-US-01);
    II. United States Patent Number 6,015,673 entitled ``Cloning and 
Expression of cDNA for Human Dihydropyrimidine Dehydrogenase,'' issued 
January 18, 2000 (HHS Ref. No. E-157-1994/0-US-03);
    III. United States Patent Number 6,787,306 entitled ``Methods and 
Compositions for Detecting Dihydropyrimidine Dehydrogenase Splicing 
Mutations,'' issued September 7, 2004 (HHS Ref. No. E-157-1994/1-US-
01);
    IV. United States Pre-Grant Publication number 2005/0136433A1 
corresponding to application serial number 10/911237 entitled ``Methods 
and Compositions for Detecting Dihydropyrimidine Dehydrogenase Splicing 
Mutations,'' published June 23, 2005 (HHS Ref. No. E-157-1994/1-US-19) 
and all issued and pending counterparts in Europe, Canada, and 
Australia.

Next Step: Teleconference

    There will be a teleconference where the principal investigator 
will explain this technology. Licensing and collaborative research 
opportunities will also be discussed. If you are interested in 
participating in this teleconference please call or e-mail Mojdeh 
Bahar; (301) 435-2950; baharm@mail.nih.gov. OTT will then e-mail you 
the date, time and number for the teleconference.

    Dated: June 26, 2008.
Richard U. Rodriguez,
Director, Division of Technology Development and Transfer, Office of 
Technology Transfer. National Institutes of Health.
[FR Doc. E8-15182 Filed 7-2-08; 8:45 am]
BILLING CODE 4140-01-P
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