National Institutes of Health, Public Health Service, HHS.
The inventions listed below are owned by an agency of the U.S. Government and are available for licensing in the U.S. in accordance with 35 U.S.C. 207 to achieve expeditious commercialization of results of federally-funded research and development. Foreign patent applications are filed on selected inventions to extend market coverage for companies and may also be available for licensing.
Licensing information and copies of the U.S. patent applications listed below may be obtained by writing to the indicated licensing contact at the Office of Technology Transfer, National Institutes of Health, 6011 Executive Boulevard, Suite 325, Rockville, Maryland 20852-3804; telephone: 301/496-7057; fax: 301/402-0220. A signed Confidential Disclosure Agreement will be required to receive copies of the patent applications.
Antibody and Immunotoxin Treatments for Mesothelin-Expressing Cancers
Description of Technology: Mesothelin is a cell surface protein that is highly expressed in aggressive cancers such as malignant mesothelioma, ovarian cancer and pancreatic cancer. As a result, mesothelin is an excellent candidate for tumor targeted immunotherapeutics. However, the antibodies against mesothelin that are available for clinical trials are of murine origin. These antibodies have the potential to elicit immune responses in patients, which may adversely affect the ability to provide patients with repeated doses. Thus, the clinical application of the antibodies may be limited.
In order to address the issue of immunogenicity in patients, NIH inventors have generated anti-mesothelin antibody variable fragments (Fv) of human origin. These antibody fragments (HN1 and HN2) have the ability to efficiently recognize mesothelin on the surface of numerous cancer cells. As a result, these antibody fragments represent an attractive therapeutic alternative to the murine anti-mesothelin antibodies currently being tested in clinical trials.
- Use as an antibody therapeutic for mesotheliomas, pancreatic tumors and ovarian tumors.
- Use in an immunotoxin therapeutic for mesotheliomas, pancreatic tumors and ovarian tumors.
- Diagnostic for the detection of mesothelin positive tumors.
- Research agent for the detection of mesothelin.
- Fully human antibody reduces potential immunogenicity, thereby allowing repeated dosing.
- Antibody specificity improves the therapeutic efficacy of the agent.
Development Status: Preclinical stage of development with some pre-clinical data available.
Inventors: Mitchell Ho et al. (NCI).
Patent Status: U.S. Provisional Application No. 61/162,778, filed 24 Mar 2009 (HHS Reference E-091-2009/0-US-01)
- U.S. Patent 6,083,502 entitled “Mesothelium Antigen and Methods and Kits For Targeting It.”
- PCT Application PCT/US97/0224 entitled “Mesothelium Antigen and Methods and Kits For Targeting It.”
- U.S. Patent 6,809,184 entitled “Antibodies, Including Fv Molecules, and Immunoconjugates Having High Binding Affinity for Mesothelin and Methods for Their Use.”
- PCT Application PCT/US98/25270 entitled “Antibodies, Including Fv Molecules, and Immunoconjugates Having High Binding Affinity for Mesothelin and Methods for Their Use.”
- U.S. Patent 7,081,518 entitled “Anti-mesothelin antibodies having high binding affinity.”
- PCT Application PCT/US00/14829 entitled “Immunoconjugates Having High Binding Affinity Improvement of scFVsr Ab's with Higher Affinity for Mesothelin.”
Licensing Status: Available for licensing.
Licensing Contact: David A. Lambertson, Ph.D.; 301-435-4632; firstname.lastname@example.org.
Collaborative Research Opportunity: The National Cancer Institute Laboratory of Molecular Biology is seeking statements of capability or interest from parties interested in collaborative research to further Start Printed Page 23730develop, evaluate, or commercialize antibody-based treatments of mesothelin-expressing cancers. Please contact John D. Hewes, Ph.D. at 301-435-3121 or email@example.com for more information.
Simple Biosensors Based on Electrical Percolation Biological Semiconductors
Description of Technology: The invention offered for licensing is in the field of biosensors with application in diagnostics and in regulation of implantable biomedical devices. More specifically, it is related to biological semiconductors based on the electrical percolation of single-walled carbon nanotubes (SWNTs). The nanotubes are embedded with biological ligands (e.g., antibodies). The electrical resistance of a semiconducting SWNT is found to dramatically increase upon the actuation by a specific antigen. Measurement of the change in resistance correlates with the concentration of the specific antigen and thus provides for quantitative determination and diagnostics of biological samples. The simple printing fabrication of electrical percolation biological semiconductors (EPBSC) can facilitate assembly of numerous types of gates (e.g., antibodies, DNA, etc.) and print many of such gates on the same chip for the creation of biological CPUs for various biomedical applications, including direct biodetection and regulation of implantable biomedical devices.
(a) Miniaturized biosensors for various biomedical applications, including: (i) Direct biodetection of microbial pathogens and their toxins ii) diagnostics and prognostics of human diseases (e.g., cancer, cardiovascular, or other biomarkers) (iii) detection and analysis of nucleic acids (e.g., DNA, RNA) (iv) detection and analysis of other analytes (carbohydrates, fatty acids, organic or inorganic compounds).
—Point of Care (POC) diagnostics (e.g., Physician's office, home-use)
—Military applications (e.g., remote sensing of biowarfare agents)
(b) Monitor food safety and detection of environmental pollution.
(c) Regulation of implantable biomedical devices such as insulin pumps or artificial hearts.
(d) New generation of personal detectors (e.g., food allergens, cardiovascular event, etc.).
(a) The electrical percolation biological semiconductors (EPBSC) are relatively simple to assemble, and do not require specialized fabrication facilities or experience which may broaden the use of EPBSC in a similar way that PDMS (Polydimethylsiloxane) technology has broadened the use of lab-on-a-chip.
(b) Many EPBSC can be fabricated into the same chip enabling simultaneous detection of many analytes.
(c) Electronic based EPBS detection enable simple digital signal amplification and analysis.
(d) EPBSC can be relatively stable with respect to retention of biological viability and thus can be stored for a long period of time before use.
(e) EPBSC enable device miniaturization.
(f) EPBSC are relatively simple to use and may not require special equipment or a skilled operator. Thus, these biosensors can be utilized in a Physician Office setting, for military applications and for possibly remote sensing for detections of biowarfare materials.
(g) EPBSC devices will offer speed of detection, ease of use, and it will be inexpensive to make.
Development Status: Proof of concept was demonstrated. For example, using anti-Staphylococcal Enterotoxin B (SEB) IgG antibodies as a gate, and the SEB antigen as an actuator, the inventors could detect as little as 0.1 ng/mL of SEB.
Market: According to market research reports from 2003-2004 the global market for biosensors was projected to grow from approximately $7.0 billion in 2004 to approximately $9.5 billion in 2009, an average annual growth of about 7.0%. Ninety-nine percent (99%) of the biosensor's market is dominated by biomedical and life sciences, while only one percent (1.0%) with applications in environmental monitoring.
Because of the unique advantages offered by this technology (i.e., diversity of applications, simplicity of use and low cost), there is a good probability that if technically successful it will become commercially successful and financially rewarding.
Inventors: Avraham Rasooly (NCI) et al.
Patent Status: U.S. Provisional Application No. 61/115,546 filed 18 Nov 2008, entitled “Electrical Percolation Biomedical Semiconductors” (HHS Reference No. E-040-2009/0-US-01).
Licensing Status: Available for licensing.
Collaborative Research Opportunity: The National Cancer Institute, Cancer Diagnostic Program, and the Food and Drug Administration, the Center for Devices and Radiological Health, Office of Science and Engineering Laboratories, is seeking statements of capability or interest from parties interested in collaborative research to further develop, evaluate, or commercialize Electrical Percolation Biological Semiconductors for biodetection. Please contact John D. Hewes, Ph.D. at 301-435-3121 or firstname.lastname@example.org for more information.
C57BL/6J Embryonic Stem Cell Lines Generated Using Serum-Free Media
Description of Technology: NIH investigators have generated Embryonic Stem (ES) cell clones from C57BL/6J mice in a defined medium. These cell lines enable direct genetic alteration of mice in a pure genetic background.
Using a defined media supplement, knockout serum replacement (KSR) with knockout DMEM (KSR-KDMEM), the investigators established ES cell lines from blastocysts of C57BL/6J mice. One specific cell line, HGTC-8 was found to be karyotypically stable and germline competent, both prior to manipulation and after gene targeting. These cell lines transfected more efficiently, and exhibited increased efficiencies of cell cloning and chimera generation, when maintained in KSR-KDMEM.
- Generation of knockout mice without the need to backcross.
- Generation of mice via targeted mutations.
Inventors: Jun Cheng, Lisa Garrett-Beal, and Pamela L. Schwartzberg (NHGRI).
Publication: J Cheng, A Dutra, A Takesono, L Garrett-Beal, PL Schwartzberg. Improved generation of C57BL/6J mouse embryonic stem cells in a defined serum-free media. Genesis. 2004 June; 39(2):100-104.
Patent Status: HHS Reference No. E-038-2009/0—Research Tool. Patent protection is not being pursued for this technology.
Licensing Status: Available for licensing under a Biological Materials License Agreement.
Licensing Contact: Suryanarayana (Sury) Vepa, Ph.D., J.D.; 301-435-5020; email@example.com.
Identification of Renal Cell Carcinoma Biomarkers
Description of Technology: This invention describes the identification of potential renal cancer biomarkers which could be utilized in the development of a renal cancer diagnostics. The invention identified cancer protein biomarkers from clinically relevant samples including peripheral blood and Start Printed Page 23731fresh frozen tissues. Vast availability of fresh frozen tissues and peripheral blood specimens that are easily obtained could lead to clinical tests amenable to therapeutic, prognostic and even early screening tests for renal cell carcinoma and other malignancies.
Applications: Renal cell carcinoma diagnostics, therapeutics and prognostics.
- Cancer is the second leading cause of death in the U.S.A. There is an acute need for cancer biomarkers that can be detected from clinically relevant samples and used for early diagnosis, therapeutic follow-up and prognosis of malignant diseases.
- The incidence of renal cell cancer has been rising steadily. Renal Cell Carcinoma is the most common type of kidney cancer, and the most common type in adults, responsible for approximately 80% of cases.
Inventors: Josip Blonder et al. (NCI).
Patent Status: PCT Application No. PCT/US2009/037855 filed 20 Mar 2009 (HHS Reference No. E-317-2008/0-PCT-01)
Licensing Status: Available for licensing.
Licensing Contact: Betty B. Tong, Ph.D.; 301-594-6565; firstname.lastname@example.org.
Collaborative Research Opportunity: The National Cancer Institute Laboratory of Proteomics and Analytical Technologies is seeking statements of capability or interest from parties interested in collaborative research to further develop, evaluate, or commercialize diagnostic, therapeutic and prognostic cancer biomarkers from clinical specimens. Please contact John D. Hewes, Ph.D. at 301-435-3121 or email@example.com for more information.Start Signature
Dated: May 13, 2009.
Richard U. Rodriguez,
Director, Division of Technology Development and Transfer, Office of Technology Transfer, National Institutes of Health.
[FR Doc. E9-11705 Filed 5-19-09; 8:45 am]
BILLING CODE 4140-01-P