Government-Owned Inventions; Availability for Licensing, 48997-48998 [2012-20059]
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Federal Register / Vol. 77, No. 158 / Wednesday, August 15, 2012 / Notices
research and testing priorities, and
providing information to regulatory
agencies about alternative methods for
toxicity screening. The NTP welcomes
nominations of scientific experts for
upcoming panels. Scientists interested
in serving on an NTP panel should
provide a current curriculum vitae to
the Contact Person. The authority for
NTP panels is provided by 42 U.S.C.
217a; section 222 of the Public Health
Service (PHS) Act, as amended. The
panel is governed by the Federal
Advisory Committee Act, as amended (5
U.S.C. Appendix 2), which sets forth
standards for the formation and use of
advisory committees.
Dated: August 8, 2012.
John R. Bucher,
Associate Director, National Toxicology
Program.
[FR Doc. 2012–20044 Filed 8–14–12; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Government-Owned Inventions;
Availability for Licensing
National Institutes of Health,
Public Health Service, HHS.
ACTION: Notice.
AGENCY:
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.
FOR FURTHER INFORMATION CONTACT:
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.
srobinson on DSK4SPTVN1PROD with NOTICES
SUMMARY:
Quick2Insight: 3D Biological Tissue
Image Rendering Software
Description of Technology: Available
for licensing for commercialization or
internal use is software providing
automatic visualization of features
VerDate Mar<15>2010
17:49 Aug 14, 2012
Jkt 226001
inside biological image volumes in 3D.
The software provides a simple and
interactive visualization for the
exploration of biological datasets
through dataset-specific transfer
functions and direct volume rendering.
The method employs a K–Means++
clustering algorithm to classify a twodimensional histogram created from the
input volume. The classification process
utilizes spatial and data properties from
the volume. Then using properties
derived from the classified clusters the
software automatically generates color
and opacity transfer functions and
presents the user with a high quality
initial rendering of the volume data.
User input can be incorporated through
the simple yet intuitive interface for
transfer function manipulation included
in our framework. Our new interface
helps users focus on feature space
exploration instead of the usual effort
intensive, low-level widget
manipulation.
Potential Commercial Applications:
• Biological tissue visualization in 3D
• Research uses
Competitive Advantages:
• User friendly
• Intuitive interface
Development Stage: Prototype
Inventors: Yanling Liu, Jack Collins,
Curtis Lisle (all of FCRDC/SAIC)
Publications:
1. Maciejewski R, et al. Structuring feature
space: a non-parametric method for
volumetric transfer function generation. IEEE
Trans Vis Comput Graphics. 2009 Nov–
Dec;15(6):1473–80. [PMID 19834223]
2. Zhou J, Takatsuka M. Automatic transfer
function generation using contour tree
controlled residue flow model and color
harmonics. IEEE Trans Vis Comput Graphics.
2009 Nov–Dec;15(6):1481–8. [PMID
19834224]
¨
3. Rottger S, et al. Spatialized Transfer
Functions. In: Brodlie K, Duke DJ, and Joy KI
(eds.) EuroVis05 Joint Eurographics—IEEE
VGTC Symposium on Visualization 1–3 June
2005, Leeds, United Kingdom, pp. 271–278.
[doi: 10.2312/VisSym/EuroVis05/271–278]
Intellectual Property: HHS Reference
No. E–254–2012/0 — Software Research
Tool. Patent protection is not being
pursued for this technology.
Licensing Contact: Michael
Shmilovich; 301–435–5019;
shmilovm@mail.nih.gov.
Collaborative Research Opportunity:
The National Cancer Institute is seeking
statements of capability or interest from
parties interested in collaborative
research to further develop, evaluate or
commercialize automatic 3D
visualization of biological image
volumes. For collaboration
opportunities, please contact John
Hewes, Ph.D. at hewesj@mail.nih.gov.
PO 00000
Frm 00050
Fmt 4703
Sfmt 4703
48997
Human Renal Epithelial Tubular Cells
for Studies of Cystinosis
Description of Technology: Cystinosis
is a rare lysosomal storage disease,
affecting about 500 people (mostly
children) in the United States and about
2000 people worldwide. It is an
autosomal recessive disorder, wherein
patients have a defect in the CTNS gene,
which codes for the lysosomal cystine
transporter. In this disorder, cystine (an
amino acid) is not properly transported
out of the lysosome and accumulates in
the cells, forming damaging crystals. As
a result, cystinosis slowly destroys
various organs in the body, including
kidneys, liver, muscles, eyes, and brain.
Currently, the only treatment for
cystinosis is cysteamine, a drug that
reduces intracellular cystine levels,
although this treatment requires
frequent dosing.
Available from NHGRI are human
renal epithelial tubular cells isolated
from cystinosis patient samples. These
cells may be useful for studying the
biology of cystinosis, as well as the
metabolic role of the lysosomal cystine
transporter; they may also be useful for
the development of screening assays for
potential therapeutic agents for
cystinosis.
Potential Commercial Applications:
• Use in studies focused on cystinosis
and lysosomal metabolism
• Use in assays for high throughput
screening of potential therapeutic agents
Competitive Advantages: These cell
lines were derived from cystinosis
patient samples, and studies performed
using these cells are expected to
correlate well to the initiation,
progression and treatment of cystinosis
in patients.
Development Stage: Early-stage
Inventor: William A. Gahl (NHGRI)
Intellectual Property: HHS Reference
No. E–204–2012/0—Research Tool.
Patent protection is not being pursued
for this technology.
Licensing Contact: Tara L. Kirby,
Ph.D.; 301–435–4426;
tarak@mail.nih.gov.
Context Aware Mobile Device Software
for Substance Abuse Interventions and
Behavioral Modification
Description of Technology: Available
for licensing for commercial
development is software that provides
personalized feedback for treating drug
dependence and associated risky
behaviors. The tool is designed for both
healthcare providers at the point-of-care
and for self-help. Many people who
could benefit from treatment do not
receive it because of its low availability
and high cost. The available software
E:\FR\FM\15AUN1.SGM
15AUN1
48998
Federal Register / Vol. 77, No. 158 / Wednesday, August 15, 2012 / Notices
‘‘mPAL’’ (Mobile Personalized
Assessment and Learning), combines
mHealth-based educational functions
with the Ecological Momentary
Assessment (EMA) functions of TED
(transactional electronic diary) software.
mPAL allows interchange of data
obtained from EMA and learning system
in order to deliver context-aware
intervention in real time, customized to
the individual needs of participants.
mPAL enables participants to interact
with educational materials at the time
and place of their choosing and receive
personalized feedback when and where
it is most needed. The software
integrates into HuRlS where
comprehensive patient data can be
leveraged alongside the mPAL data to
provide better understanding of the
underlying factors under investigation.
Potential Commercial Applications:
• Substance abuse
• Drug abuse
• Alcoholism
• Behavioral modification
• Smoking cessation
• Pain management
Competitive Advantages:
• Low-cost mobile treatment
mechanism
• Provides personalized feedback to
patients at the time and place they
choose
• Proven usability in prior clinical
studies
Development Stage: Clinical
Inventors: Massoud R. Vahabzadeh,
Mustapha Mezghanni, and Jia-Ling Lin
(all of NIDA)
Publications:
srobinson on DSK4SPTVN1PROD with NOTICES
1. Vahabzadeh M, et al. PGIS: Electronic
diary data integration with GPS data initial
application in substance-abuse patients. In,
Proc. 23rd IEEE International Symposium on
Computer-Based Medical Systems, pp 474–9,
2010. [DOI: 10.1109/CBMS.2010.6042691]
2. Lin JL, et al. A high-level specification
for adaptive ecological momentary
assessment: real-time assessment of drug
craving, use and abstinence. AMIA Annu
Symp Proc. 2005:455–9. [PMID 16779081]
3. Vahabzadeh M, et al. An electronic diary
software for ecological momentary
assessment (EMA) in clinical trials. In, Proc.
17th IEEE International Symposium on
Computer-Based Medical Systems, pp 167–
72, 2004. [DOI: 10.1109/
CBMS.2004.1311709]
Intellectual Property: HHS Reference
No. E–195–2012/0—Software. Patent
protection is not being pursued for this
technology.
Licensing Contact: Michael
Shmilovich; 301–435–5019;
shmilovm@mail.nih.gov.
Collaborative Research Opportunity:
The NIDA, IRP, Biomedical Informatics
Section, is seeking statements of
capability or interest from parties
VerDate Mar<15>2010
17:49 Aug 14, 2012
Jkt 226001
interested in collaborative research to
further develop, evaluate or
commercialize Mobile Personalized
Assessment & Learning for Addiction
Treatment and Behavioral Modification.
For collaboration opportunities, please
contact Vio Conley at
conleyv@mail.nih.gov.
Dated: August 10, 2012.
Richard U. Rodriguez,
Director, Division of Technology Development
and Transfer, Office of Technology Transfer,
National Institutes of Health.
Plasmid Useful in Transplantation
Therapy for Age-Related Eye Disease
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Description of Technology:
Researchers have developed a green
fluorescent protein (GFP) based plasmid
that can be used to detect differentiated
retinal pigment epithelium (RPE) cells.
RPE is a layer of cells located behind the
eye that becomes damaged in agerelated macular degeneration (AMD).
Current cell based therapies for treating
AMD focus on generating RPE cells from
stem cells. This GPF-based plasmid can
be inserted into growing stem cells, and
the fluorescence marker can be used to
detect and purify stem cells
differentiating into RPE cells. This
advancement allows generation of a
purified population of RPE cells for in
vitro and transplantation purposes.
Additionally, cells comprising the
GFP-based construct may be useful in
high-throughput drug screening as a
means to: (1) identify potential
therapeutic targets of RPE degenerative
diseases such as AMD, and (2) evaluate
initial toxicity of candidate drugs in
RPE cells.
Potential Commercial Applications:
• Fluorescence based marker for
detecting and purifying differentiated
RPE cells
• Potential use in high throughput
drug screening
Competitive Advantages: GFP based
marker allows for fast and simple
detection of differentiated RPE cells
from stem cells.
Development Stage:
• Prototype
• In vitro data available
Inventors: Kapil Bharti (NINDS),
Heinz Arnheiter (NINDS), Sheldon
Millier (NEI)
Publication: Bharti K, et al. The new
paradigm: retinal pigment epithelium
cells generated from embryonic or
induced pluripotent stem cells. Pigment
Cell Melanoma Res. 2011 Feb;24(1):21–
34. [PMID 20846177]
Intellectual Property: HHS Reference
No. E–054–2012/0—Research Tool.
Patent protection is not being pursued
for this technology.
Licensing Contact: Lauren NguyenAntczak, Ph.D., J.D.; 301–435–4074;
lauren.nguyen-antczak@nih.gov.
PO 00000
Frm 00051
Fmt 4703
Sfmt 4703
[FR Doc. 2012–20059 Filed 8–14–12; 8:45 am]
BILLING CODE 4140–01–P
National Institutes of Health
National Institute of Mental Health;
Notice of Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of a meeting of the
National Advisory Mental Health
Council.
The meeting will be open to the
public as indicated below, with
attendance limited to space available.
Individuals who plan to attend and
need special assistance, such as sign
language interpretation or other
reasonable accommodations, should
notify the Contact Person listed below
in advance of the 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 Advisory
Mental Health Council.
Date: September 13, 2012.
Open: 8:30 a.m. to 2 p.m.
Agenda: Presentation of NIMH Director’s
report and discussion on NIMH program and
policy issues.
Place: National Institutes of Health
Neuroscience Center, 6001 Executive
Boulevard, Conference Room C/D/E,
Rockville, MD 20852.
Closed: 2:30 p.m. to 5 p.m.
Agenda: To review and evaluate grant
applications
Place: National Institutes of Health
Neuroscience Center, 6001 Executive
Boulevard, Conference Room C/D/E,
Rockville, MD 20852.
Contact Person: Jane A. Steinberg, Ph.D.,
Director, Division of Extramural Activities,
National Institute of Mental Health, NIH,
Neuroscience Center, 6001 Executive Blvd.,
Room 6154, MSC 9609, Bethesda, MD 20892–
9609, 301–443–5047.
Any member of the public interested in
presenting oral comments to the committee
may notify the Contact Person listed on this
E:\FR\FM\15AUN1.SGM
15AUN1
Agencies
[Federal Register Volume 77, Number 158 (Wednesday, August 15, 2012)]
[Notices]
[Pages 48997-48998]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-20059]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Government-Owned Inventions; Availability for Licensing
AGENCY: National Institutes of Health, Public Health Service, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: 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.
FOR FURTHER INFORMATION CONTACT: 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.
Quick2Insight: 3D Biological Tissue Image Rendering Software
Description of Technology: Available for licensing for
commercialization or internal use is software providing automatic
visualization of features inside biological image volumes in 3D. The
software provides a simple and interactive visualization for the
exploration of biological datasets through dataset-specific transfer
functions and direct volume rendering. The method employs a K-Means++
clustering algorithm to classify a two-dimensional histogram created
from the input volume. The classification process utilizes spatial and
data properties from the volume. Then using properties derived from the
classified clusters the software automatically generates color and
opacity transfer functions and presents the user with a high quality
initial rendering of the volume data. User input can be incorporated
through the simple yet intuitive interface for transfer function
manipulation included in our framework. Our new interface helps users
focus on feature space exploration instead of the usual effort
intensive, low-level widget manipulation.
Potential Commercial Applications:
Biological tissue visualization in 3D
Research uses
Competitive Advantages:
User friendly
Intuitive interface
Development Stage: Prototype
Inventors: Yanling Liu, Jack Collins, Curtis Lisle (all of FCRDC/
SAIC)
Publications:
1. Maciejewski R, et al. Structuring feature space: a non-
parametric method for volumetric transfer function generation. IEEE
Trans Vis Comput Graphics. 2009 Nov-Dec;15(6):1473-80. [PMID
19834223]
2. Zhou J, Takatsuka M. Automatic transfer function generation
using contour tree controlled residue flow model and color
harmonics. IEEE Trans Vis Comput Graphics. 2009 Nov-Dec;15(6):1481-
8. [PMID 19834224]
3. R[ouml]ttger S, et al. Spatialized Transfer Functions. In:
Brodlie K, Duke DJ, and Joy KI (eds.) EuroVis05 Joint Eurographics--
IEEE VGTC Symposium on Visualization 1-3 June 2005, Leeds, United
Kingdom, pp. 271-278. [doi: 10.2312/VisSym/EuroVis05/271-278]
Intellectual Property: HHS Reference No. E-254-2012/0 -- Software
Research Tool. Patent protection is not being pursued for this
technology.
Licensing Contact: Michael Shmilovich; 301-435-5019;
shmilovm@mail.nih.gov.
Collaborative Research Opportunity: The National Cancer Institute
is seeking statements of capability or interest from parties interested
in collaborative research to further develop, evaluate or commercialize
automatic 3D visualization of biological image volumes. For
collaboration opportunities, please contact John Hewes, Ph.D. at
hewesj@mail.nih.gov.
Human Renal Epithelial Tubular Cells for Studies of Cystinosis
Description of Technology: Cystinosis is a rare lysosomal storage
disease, affecting about 500 people (mostly children) in the United
States and about 2000 people worldwide. It is an autosomal recessive
disorder, wherein patients have a defect in the CTNS gene, which codes
for the lysosomal cystine transporter. In this disorder, cystine (an
amino acid) is not properly transported out of the lysosome and
accumulates in the cells, forming damaging crystals. As a result,
cystinosis slowly destroys various organs in the body, including
kidneys, liver, muscles, eyes, and brain. Currently, the only treatment
for cystinosis is cysteamine, a drug that reduces intracellular cystine
levels, although this treatment requires frequent dosing.
Available from NHGRI are human renal epithelial tubular cells
isolated from cystinosis patient samples. These cells may be useful for
studying the biology of cystinosis, as well as the metabolic role of
the lysosomal cystine transporter; they may also be useful for the
development of screening assays for potential therapeutic agents for
cystinosis.
Potential Commercial Applications:
Use in studies focused on cystinosis and lysosomal
metabolism
Use in assays for high throughput screening of potential
therapeutic agents
Competitive Advantages: These cell lines were derived from
cystinosis patient samples, and studies performed using these cells are
expected to correlate well to the initiation, progression and treatment
of cystinosis in patients.
Development Stage: Early-stage
Inventor: William A. Gahl (NHGRI)
Intellectual Property: HHS Reference No. E-204-2012/0--Research
Tool. Patent protection is not being pursued for this technology.
Licensing Contact: Tara L. Kirby, Ph.D.; 301-435-4426;
tarak@mail.nih.gov.
Context Aware Mobile Device Software for Substance Abuse Interventions
and Behavioral Modification
Description of Technology: Available for licensing for commercial
development is software that provides personalized feedback for
treating drug dependence and associated risky behaviors. The tool is
designed for both healthcare providers at the point-of-care and for
self-help. Many people who could benefit from treatment do not receive
it because of its low availability and high cost. The available
software
[[Page 48998]]
``mPAL'' (Mobile Personalized Assessment and Learning), combines
mHealth-based educational functions with the Ecological Momentary
Assessment (EMA) functions of TED (transactional electronic diary)
software. mPAL allows interchange of data obtained from EMA and
learning system in order to deliver context-aware intervention in real
time, customized to the individual needs of participants. mPAL enables
participants to interact with educational materials at the time and
place of their choosing and receive personalized feedback when and
where it is most needed. The software integrates into HuRlS where
comprehensive patient data can be leveraged alongside the mPAL data to
provide better understanding of the underlying factors under
investigation.
Potential Commercial Applications:
Substance abuse
Drug abuse
Alcoholism
Behavioral modification
Smoking cessation
Pain management
Competitive Advantages:
Low-cost mobile treatment mechanism
Provides personalized feedback to patients at the time and
place they choose
Proven usability in prior clinical studies
Development Stage: Clinical
Inventors: Massoud R. Vahabzadeh, Mustapha Mezghanni, and Jia-Ling
Lin (all of NIDA)
Publications:
1. Vahabzadeh M, et al. PGIS: Electronic diary data integration
with GPS data initial application in substance-abuse patients. In,
Proc. 23rd IEEE International Symposium on Computer-Based Medical
Systems, pp 474-9, 2010. [DOI: 10.1109/CBMS.2010.6042691]
2. Lin JL, et al. A high-level specification for adaptive
ecological momentary assessment: real-time assessment of drug
craving, use and abstinence. AMIA Annu Symp Proc. 2005:455-9. [PMID
16779081]
3. Vahabzadeh M, et al. An electronic diary software for
ecological momentary assessment (EMA) in clinical trials. In, Proc.
17th IEEE International Symposium on Computer-Based Medical Systems,
pp 167-72, 2004. [DOI: 10.1109/CBMS.2004.1311709]
Intellectual Property: HHS Reference No. E-195-2012/0--Software.
Patent protection is not being pursued for this technology.
Licensing Contact: Michael Shmilovich; 301-435-5019;
shmilovm@mail.nih.gov.
Collaborative Research Opportunity: The NIDA, IRP, Biomedical
Informatics Section, is seeking statements of capability or interest
from parties interested in collaborative research to further develop,
evaluate or commercialize Mobile Personalized Assessment & Learning for
Addiction Treatment and Behavioral Modification. For collaboration
opportunities, please contact Vio Conley at conleyv@mail.nih.gov.
Plasmid Useful in Transplantation Therapy for Age-Related Eye Disease
Description of Technology: Researchers have developed a green
fluorescent protein (GFP) based plasmid that can be used to detect
differentiated retinal pigment epithelium (RPE) cells. RPE is a layer
of cells located behind the eye that becomes damaged in age-related
macular degeneration (AMD). Current cell based therapies for treating
AMD focus on generating RPE cells from stem cells. This GPF-based
plasmid can be inserted into growing stem cells, and the fluorescence
marker can be used to detect and purify stem cells differentiating into
RPE cells. This advancement allows generation of a purified population
of RPE cells for in vitro and transplantation purposes.
Additionally, cells comprising the GFP-based construct may be
useful in high-throughput drug screening as a means to: (1) identify
potential therapeutic targets of RPE degenerative diseases such as AMD,
and (2) evaluate initial toxicity of candidate drugs in RPE cells.
Potential Commercial Applications:
Fluorescence based marker for detecting and purifying
differentiated RPE cells
Potential use in high throughput drug screening
Competitive Advantages: GFP based marker allows for fast and simple
detection of differentiated RPE cells from stem cells.
Development Stage:
Prototype
In vitro data available
Inventors: Kapil Bharti (NINDS), Heinz Arnheiter (NINDS), Sheldon
Millier (NEI)
Publication: Bharti K, et al. The new paradigm: retinal pigment
epithelium cells generated from embryonic or induced pluripotent stem
cells. Pigment Cell Melanoma Res. 2011 Feb;24(1):21-34. [PMID 20846177]
Intellectual Property: HHS Reference No. E-054-2012/0--Research
Tool. Patent protection is not being pursued for this technology.
Licensing Contact: Lauren Nguyen-Antczak, Ph.D., J.D.; 301-435-
4074; lauren.nguyen-antczak@nih.gov.
Dated: August 10, 2012.
Richard U. Rodriguez,
Director, Division of Technology Development and Transfer, Office of
Technology Transfer, National Institutes of Health.
[FR Doc. 2012-20059 Filed 8-14-12; 8:45 am]
BILLING CODE 4140-01-P