Government-Owned Inventions; Availability for Licensing, 22820-22822 [2014-09354]
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22820
Federal Register / Vol. 79, No. 79 / Thursday, April 24, 2014 / Notices
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[FR Doc. 2014–09344 Filed 4–23–14; 8:45 am]
BILLING CODE 4184–35–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Government-Owned Inventions;
Availability for Licensing
AGENCY:
National Institutes of Health,
HHS.
ACTION:
Notice.
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. 209 and 37 CFR Part 404 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.
pmangrum on DSK3VPTVN1PROD with NOTICES
SUMMARY:
Use of Antihistamine Compounds for
the Treatment of Hepatitis C Virus
Description of Technology: The vast
majority of people infected with
Hepatitis C Virus (HCV) will have
chronic infection. Over decades, this
can lead to liver disease and liver
cancer. In fact, HCV infection is the
leading cause of liver transplants in the
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14:19 Apr 23, 2014
Jkt 232001
U.S. Several new drugs have recently
come into the market that will likely
change the HCV treatment paradigm.
However, the effectiveness of these new
drugs can vary depending on the HCV
genotype. Thus, there is still the need
for additional new therapeutics against
HCV.
The subject technology are small
molecule compounds identified using a
novel cell-based high throughput assay
of HCV infection. The compounds are
antihistamines that show potent
antiviral properties against HCV. One
advantage of these compounds is that
they are already on the market for the
treatment of allergic reactions and, thus,
have been used extensively in humans
and have excellent safety profiles with
known pharmaceutical properties. The
subject technology can also potentially
be used in combination with other HCV
therapeutics.
Potential Commercial Applications:
Prevention or treatment of HCV
infection.
Competitive Advantages: These
compounds are already on the market
and, thus, have known safety profiles
and pharmaceutical properties.
Development Stage
• Early-stage
• In vitro data available
Inventors: Jake Tsanyang Liang
(NIDDK), Juan Jose Marugan (NCATS),
Noel Terrance Southhall (NCATS), Xin
Hu (NCATS), Jingbo Xiao (NCATS),
Shanshan He (NIDDK), Marc Ferrer
(NCATS), Zongyi Hu (NIDDK), Wei
Zhang (NCATS)
Intellectual Property: HHS Reference
No. E–011–2014/0—US Provisional
Patent Application No. 61/909,414 filed
27 Nov 2013
Licensing Contact: Kevin W. Chang,
Ph.D.; 301–435–5018; changke@
mail.nih.gov
Intranasal Nebulizer With Disposable
Drug Cartridge for Improved Delivery
of Vaccines and Therapeutics
Description of Technology: Intranasal
delivery is a simple, inexpensive and
needle-free route for administration of
vaccines and therapeutics. This
intranasal delivery technology,
developed with Creare LLC, includes
low-cost, disposable drug cartridges
(DDCs) that mate with a durable handheld device. The rechargeable-batterypowered device transmits ultrasonic
energy to the DDC to aerosolize the drug
and is capable of performing for eight
hours at 120 vaccinations per hour.
Potential applications for this platform
technology include intranasal
vaccination (e.g. seasonal or pandemic
influenza vaccines) and intranasal
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Fmt 4703
Sfmt 4703
delivery of locally active (e.g.
antihistamines, steroids) or systemically
active (e.g. pain medications, sedatives)
pharmaceuticals.
The DDCs themselves offer two
unique benefits. First, all components
that contact the active agent or the
patient may be easily disposed of,
which reduces the risk of patient crosscontamination and minimizes cleaning
and maintenance requirements of the
hand-held device. Second, DDCs
provide a low-cost and simple method
to package and distribute individual
doses.
This technology also allows for
significant dose-sparing. Preliminary
studies have shown robust immune
responses when this technology is used
to delivery significantly reduced doses
of Live Attenuated Influenza Vaccine in
animal models. The intranasal nebulizer
produces droplets sized for optimum
depositioning in the nasal airway. The
small nebulizer droplets essentially
‘‘spray paint’’ the internal nasal airway,
resulting in an increased tissue surface
coverage that may enable a significant
dose reduction. In contrast, currently
available nasal delivery devices, such as
nasal sprays and droppers, do not
provide efficient intranasal delivery in
humans because the large droplets they
generate fail to coat a significant portion
of the nasal airway. Large droplets also
tend to drip out of the nose or down the
throat, which can be unpleasant for the
patient in addition to wasting a sizable
portion of the active agent.
Potential Commercial Applications
• Intranasal delivery of vaccines and
therapeutics
• Childhood vaccination programs,
mass immunization campaigns, or
response to epidemics
Competitive Advantages
• Safe, needle-less delivery
• No patient-to-patient contamination
• Long-life, rechargeable battery
• Consistent delivery and dose-sparing
• Nasal delivery of live-attenuated
vaccines may be more effective than
traditional injected vaccines
• Cost-effective
• Reduces biohazard waste
• May be administered by personnel
with minimal medical training
• Easy means of delivery to children
with fear of needles
Development Stage
• Prototype
• In vitro data available
• In vivo data available (animal)
Inventors: Mark J. Papania (CDC), et
al.
Publication: Smith JH, et al.
Nebulized live-attenuated influenza
E:\FR\FM\24APN1.SGM
24APN1
Federal Register / Vol. 79, No. 79 / Thursday, April 24, 2014 / Notices
vaccine provides protection in ferrets at
a reduced dose. Vaccine. 2012 Apr
19;30(19):3026–33. [PMID 22075083]
Intellectual Property
• HHS Reference No. E–308–2013/0—
—PCT Application No. PCT/US2011/
039020 filed on 03 Jun 2011, which
published as WO 2011/153406 on 08
Dec 2011
—US Patent Application No. 13/701,992
filed 04 Dec 2012
—Various international pending patents
• HHS Reference No. E–323–2013/0—
—PCT Application No. PCT/US2002/
007973 filed 13 Mar 2002, which
published as WO 2002/074372 on 26
Sep 2002
—US Patent No. 7,225,807 issued 05 Jun
2007
—US Patent No. 8,544,462 issued 01 Oct
2013
—Various international issued patents
• HHS Reference No. E–324–2013/0—
—PCT Application No. PCT/US2005/
011086 filed 01 Apr 2005, which
published as WO 2006/006963 on 19
Jan 2006
—US Patent No. 7,954,486 issued 07 Jun
2011
—US Patent No. 8,656,908 issued 25
Feb 2014
—Various international issued patents
• HHS Reference No. E–564–2013/0—
US Provisional Application No. 61/
808,547 filed 04 Apr 2013
Licensing Contact: Whitney Blair, J.D.,
M.P.H.; 301–435–4937; whitney.blair@
nih.gov
pmangrum on DSK3VPTVN1PROD with NOTICES
Silica Exposure Safety: Mini-Baghouse
Systems and Methods for Controlling
Particulate Release From Large Sand
Transfer Equipment
Description of Technology: CDC/
NIOSH scientists have developed an
effective point-source control for silicacontaining dusts that can be generated
from machinery on sites where
hydraulic fracturing is occurring. The
CDC/NIOSH mini-baghouse retrofit
assembly is a bolt-on control designed
to contain silica-containing respirable
dusts generated during refill operations
of sand movers during hydraulic
fracturing.
In the U.S., most new oil and gas
wells are hydraulically fractured to
enhance well production. Most
hydraulic fracturing operations have 2–
5 sand movers on-site which transfer
thousands to millions of pounds of
silica sand during each stage of
fracturing. While a variety of passive
and active controls are currently
available (or have been proposed) to
limit release of silica-containing dusts,
the CDC/NIOSH mini-baghouse retrofit
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14:19 Apr 23, 2014
Jkt 232001
assembly was designed to fill a unique
need for a control. The retrofit to
equipment can be made in the field,
uses existing energy inherent in the
system and is relatively simple and
effective. CDC/NIOSH field research has
shown that risks for exposure to
respirable silica arise from at least 8
points of dust generation and that a
variety of controls (engineering,
administrative and personal protective
equipment) are needed to control
exposures. Use of the mini-baghouse
retrofit technology is intended to limit
release of respirable silica from thief
hatches on top of the sand movers,
enhancing workplace health and safety.
Potential Commercial Applications
• Controlling occupational exposure to
respirable crystalline silica,
particularly during work involving
transfer of sand into sand movers on
hydraulic fracturing sites
• In-field retrofits of currently operating
heavy equipment (e.g., sand movers)
• Limiting visible dust emissions from
sand moving equipment
• Reducing respirable crystalline silica
dust emissions to enhance
compliance with OSHA PEL for silica
Competitive Advantages
• Designed for in-field retrofitting ‘‘thief
hatches’’ of existing machinery
• Uses energy inherent in the
pneumatic transfer of sand
• Provides a passive sand-movermounted control for silica release at
hydraulic fracturing operations
Development Stage
• In situ data available (on-site)
• Prototype
Inventors: Eric J. Esswein, Michael
Breitenstein, John E. Snawder, Michael
G. Gressel, Jerry L. Kratzer (all of CDC)
Publication: Esswein EJ, et al.
Occupational exposures to respirable
crystalline silica during hydraulic
fracturing. JJ Occup Environ Hyg.
2013;10(7):347–56. [PMID 23679563]
Intellectual Property: HHS Reference
No. E–291–2013/0—US Application No.
13/802,265 filed 13 Mar 2013
Licensing Contact: Whitney Blair, J.D.,
M.P.H.; 301–435–4937; whitney.blair@
nih.gov
Viral Like Particles Based Chikungunya
Vaccines
Description of Technology:
Chikungunya virus (CHIKV) is
mosquito-borne alphavirus endemic in
Africa, India, and Southeast Asia. In
2013 CHIKV infection has also emerged
in the Caribbean and a pandemic of
CHIKV has re-emerged in the
Philippines following Typhoon Haiyan.
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22821
Currently, there is no vaccine available
for the prevention of CHIKV infection
and no specific therapy exists to treat
the illness. Researchers at the Vaccine
Research Center (VRC) of the National
Institute of Allergy and Infectious
Diseases (NIAID) have developed a
CHIKV Viral Like Particle (CHIKV VLP)
vaccine based on plasmid expression
vectors encoding structural proteins of
the CHIKV virus, which gave rise to
CHIKV VLPs in transfected cells. The
CHIKV VLPs consist of the core, E1 and
E2 proteins and are similar in buoyant
density and morphology to replicationcompetent CHIKV virus. Immunization
with CHIKV VLPs elicited neutralizing
antibodies against envelope proteins
from different CHIKV strains in mouse
and nonhuman primate (NHP) models.
Monkeys immunized with CHIKV VLPs
produced high titer neutralizing
antibodies that protected against
viremia after high dose challenge. The
selected CHIKV VLP vaccine candidate,
VRC–CHKVLP059–00–VP, composed of
the E1, E2, and capsid proteins from the
CHIKV strain 37997, was recently
evaluated by the VRC at the NIH
Clinical Center for safety, tolerability
and immunogenicity in the clinical
protocol VRC 311 (ClinicalTrials.gov #
NCT01489358), a Phase I, open-label,
dose escalation clinical trial. The VRC–
CHKVLP059–00–VP vaccine was highly
immunogenic, safe, and well-tolerated.
VRC researchers have also developed
the transient transfection manufacturing
process for CHIKV and other
alphaviruses, such as Western, Eastern
and Venezuelan Equine Encephalitis
(WEVEE) viruses. Pre-clinical in vivo
mouse and NHP data, Phase 1 clinical
trial data and manufacturing data are
available.
Potential Commercial Applications:
Chikungunya vaccines based on viral
like particles.
Competitive Advantages
• There is currently no CHIKV vaccine
on the market.
• VRC–CHKVLP059–00–VP vaccine
candidate is highly immunogenic,
safe, and well-tolerated.
• Minimal containment requirements
for CHIKV VLP manufacturing
because live virus production is not
required.
Development Stage
• In vitro data available
• In vivo data available (animal)
• In vivo data available (human)
Inventors: Gary J. Nabel, Wataru
Akahata, Srinivas S. Rao (all of VRC/
NIAID)
E:\FR\FM\24APN1.SGM
24APN1
22822
Federal Register / Vol. 79, No. 79 / Thursday, April 24, 2014 / Notices
Publications
1. Akahata W, et al. A virus-like particle
vaccine for epidemic Chikungunya
virus protects non-human primates
against infection. Nat Med. 2010
Mar;16(3):334–8. [PMID 20111039]
2. Akahata W, Nabel GJ. A specific
domain of the Chikungunya virus
E2 protein regulates particle
formation in human cells:
implications for alphavirus vaccine
design. J Virol. 2012
Aug;86(16):8879–83. [PMID
22647698]
3. Chang et al. Chikungunya Virus-Like
Particle Vaccine Elicits Neutralizing
Antibodies in Healthy Adults in a
Phase I Clinical Trial; manuscript
submitted.
Intellectual Property
• HHS Reference Nos. E–004–2009/0/1/
2—
—US Provisional Application No. 61/
118,206 filed 26 Nov 2008
—US Provisional Application No. 61/
201,118 filed 05 Dec 2008
—International Application No. PCT/
US2009/006294 (WO 2010/062396)
filed 24 Nov 2009
—and corresponding filings in the US,
Europe, China, Australia, Brazil,
India, Malaysia, South Africa,
Singapore, Indonesia, Philippines and
Vietnam
• HHS Reference No. E–057–2011/0/1/
2—
—US Provisional Application No. 61/
438,236 filed 31 Jan 2011
—International Application No. PCT/
US2012/023361 (WO 2012/106356)
filed 31 Jan 2012
—and corresponding filings in the US
and India
Licensing Contact: Cristina
Thalhammer-Reyero, Ph.D., MBA; 301–
435–4507; ThalhamC@mail.nih.gov
Dated: April 21, 2014.
Richard U. Rodriguez,
Director, Division of Technology Development
and Transfer, Office of Technology Transfer,
National Institutes of Health.
[FR Doc. 2014–09354 Filed 4–23–14; 8:45 am]
BILLING CODE 4140–01–P
pmangrum on DSK3VPTVN1PROD with NOTICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Center for Scientific Review; Notice of
Closed Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meetings.
VerDate Mar<15>2010
14:19 Apr 23, 2014
Jkt 232001
The meetings 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: Center for Scientific
Review Special Emphasis Panel; PAR13–137:
Light at Night.
Date: May 20, 2014.
Time: 8:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Virtual Meeting).
Contact Person: Michael Selmanoff, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 5164,
MSC 7844, Bethesda, MD 20892, 301–435–
1119, selmanom@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Member
conflict: Drugs, Alcohol and Heavy Metals.
Date: May 21–22, 2014.
Time: 8:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892,
(Virtual Meeting).
Contact Person: Michael Selmanoff, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 5164,
MSC 7844, Bethesda, MD 20892, 301–435–
1119, selmanom@csr.nih.gov.
Name of Committee: Genes, Genomes, and
Genetics Integrated Review Group; Molecular
Genetics B Study Section.
Date: May 28–29, 2014.
Time: 5:00 p.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Admiral Fell Inn, 888 South
Broadway, Baltimore, MD 21231.
Contact Person: Richard A. Currie, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 5128,
MSC 7840, Bethesda, MD 20892, (301) 435–
1219, currieri@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; PAR Panel:
Genome x Environment.
Date: May 29–30, 2014.
Time: 8:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Time: Bethesda Marriott Suites, 6711
Democracy Boulevard, Bethesda, MD 20817.
Contact Person: Melinda Jenkins, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 3156,
PO 00000
Frm 00035
Fmt 4703
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MSC 7770, Bethesda, MD 20892, 301–437–
7872, jenkinsml2@mail.nih.gov.
Name of Committee: Immunology
Integrated Review Group; Cellular and
Molecular Immunology—B Study Section.
Date: May 29–30, 2014.
Time: 8:00 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Residence Inn Bethesda, 7335
Wisconsin Avenue, Bethesda, MD 20814.
Contact Person: Betty Hayden, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 4206,
MSC 7812, Bethesda, MD 20892, 301–435–
1223, haydenb@csr.nih.gov.
Name of Committee: Population Sciences
and Epidemiology Integrated Review Group;
Social Sciences and Population Studies A
Study Section.
Date: May 29, 2014.
Time: 8:30 a.m. to 6:30 p.m.
Agenda: To review and evaluate grant
applications.
Place: Pier 5 Hotel, 711 Eastern Avenue,
Baltimore, MD 21202.
Contact Person: Suzanne Ryan, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 3139,
MSC 7770, Bethesda, MD 20892, (301) 435–
1712, ryansj@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: April 21, 2014.
Melanie J. Gray,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2014–09353 Filed 4–23–14; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of Biomedical
Imaging and Bioengineering; Notice of
Closed Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), 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.
E:\FR\FM\24APN1.SGM
24APN1
Agencies
[Federal Register Volume 79, Number 79 (Thursday, April 24, 2014)]
[Notices]
[Pages 22820-22822]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-09354]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Government-Owned Inventions; Availability for Licensing
AGENCY: National Institutes of Health, 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. 209 and 37 CFR Part 404 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.
Use of Antihistamine Compounds for the Treatment of Hepatitis C Virus
Description of Technology: The vast majority of people infected
with Hepatitis C Virus (HCV) will have chronic infection. Over decades,
this can lead to liver disease and liver cancer. In fact, HCV infection
is the leading cause of liver transplants in the U.S. Several new drugs
have recently come into the market that will likely change the HCV
treatment paradigm. However, the effectiveness of these new drugs can
vary depending on the HCV genotype. Thus, there is still the need for
additional new therapeutics against HCV.
The subject technology are small molecule compounds identified
using a novel cell-based high throughput assay of HCV infection. The
compounds are antihistamines that show potent antiviral properties
against HCV. One advantage of these compounds is that they are already
on the market for the treatment of allergic reactions and, thus, have
been used extensively in humans and have excellent safety profiles with
known pharmaceutical properties. The subject technology can also
potentially be used in combination with other HCV therapeutics.
Potential Commercial Applications: Prevention or treatment of HCV
infection.
Competitive Advantages: These compounds are already on the market
and, thus, have known safety profiles and pharmaceutical properties.
Development Stage
Early-stage
In vitro data available
Inventors: Jake Tsanyang Liang (NIDDK), Juan Jose Marugan (NCATS),
Noel Terrance Southhall (NCATS), Xin Hu (NCATS), Jingbo Xiao (NCATS),
Shanshan He (NIDDK), Marc Ferrer (NCATS), Zongyi Hu (NIDDK), Wei Zhang
(NCATS)
Intellectual Property: HHS Reference No. E-011-2014/0--US
Provisional Patent Application No. 61/909,414 filed 27 Nov 2013
Licensing Contact: Kevin W. Chang, Ph.D.; 301-435-5018;
changke@mail.nih.gov
Intranasal Nebulizer With Disposable Drug Cartridge for Improved
Delivery of Vaccines and Therapeutics
Description of Technology: Intranasal delivery is a simple,
inexpensive and needle-free route for administration of vaccines and
therapeutics. This intranasal delivery technology, developed with
Creare LLC, includes low-cost, disposable drug cartridges (DDCs) that
mate with a durable hand-held device. The rechargeable-battery-powered
device transmits ultrasonic energy to the DDC to aerosolize the drug
and is capable of performing for eight hours at 120 vaccinations per
hour. Potential applications for this platform technology include
intranasal vaccination (e.g. seasonal or pandemic influenza vaccines)
and intranasal delivery of locally active (e.g. antihistamines,
steroids) or systemically active (e.g. pain medications, sedatives)
pharmaceuticals.
The DDCs themselves offer two unique benefits. First, all
components that contact the active agent or the patient may be easily
disposed of, which reduces the risk of patient cross-contamination and
minimizes cleaning and maintenance requirements of the hand-held
device. Second, DDCs provide a low-cost and simple method to package
and distribute individual doses.
This technology also allows for significant dose-sparing.
Preliminary studies have shown robust immune responses when this
technology is used to delivery significantly reduced doses of Live
Attenuated Influenza Vaccine in animal models. The intranasal nebulizer
produces droplets sized for optimum depositioning in the nasal airway.
The small nebulizer droplets essentially ``spray paint'' the internal
nasal airway, resulting in an increased tissue surface coverage that
may enable a significant dose reduction. In contrast, currently
available nasal delivery devices, such as nasal sprays and droppers, do
not provide efficient intranasal delivery in humans because the large
droplets they generate fail to coat a significant portion of the nasal
airway. Large droplets also tend to drip out of the nose or down the
throat, which can be unpleasant for the patient in addition to wasting
a sizable portion of the active agent.
Potential Commercial Applications
Intranasal delivery of vaccines and therapeutics
Childhood vaccination programs, mass immunization campaigns,
or response to epidemics
Competitive Advantages
Safe, needle-less delivery
No patient-to-patient contamination
Long-life, rechargeable battery
Consistent delivery and dose-sparing
Nasal delivery of live-attenuated vaccines may be more
effective than traditional injected vaccines
Cost-effective
Reduces biohazard waste
May be administered by personnel with minimal medical training
Easy means of delivery to children with fear of needles
Development Stage
Prototype
In vitro data available
In vivo data available (animal)
Inventors: Mark J. Papania (CDC), et al.
Publication: Smith JH, et al. Nebulized live-attenuated influenza
[[Page 22821]]
vaccine provides protection in ferrets at a reduced dose. Vaccine. 2012
Apr 19;30(19):3026-33. [PMID 22075083]
Intellectual Property
HHS Reference No. E-308-2013/0--
--PCT Application No. PCT/US2011/039020 filed on 03 Jun 2011, which
published as WO 2011/153406 on 08 Dec 2011
--US Patent Application No. 13/701,992 filed 04 Dec 2012
--Various international pending patents
HHS Reference No. E-323-2013/0--
--PCT Application No. PCT/US2002/007973 filed 13 Mar 2002, which
published as WO 2002/074372 on 26 Sep 2002
--US Patent No. 7,225,807 issued 05 Jun 2007
--US Patent No. 8,544,462 issued 01 Oct 2013
--Various international issued patents
HHS Reference No. E-324-2013/0--
--PCT Application No. PCT/US2005/011086 filed 01 Apr 2005, which
published as WO 2006/006963 on 19 Jan 2006
--US Patent No. 7,954,486 issued 07 Jun 2011
--US Patent No. 8,656,908 issued 25 Feb 2014
--Various international issued patents
HHS Reference No. E-564-2013/0--US Provisional Application No.
61/808,547 filed 04 Apr 2013
Licensing Contact: Whitney Blair, J.D., M.P.H.; 301-435-4937;
whitney.blair@nih.gov
Silica Exposure Safety: Mini-Baghouse Systems and Methods for
Controlling Particulate Release From Large Sand Transfer Equipment
Description of Technology: CDC/NIOSH scientists have developed an
effective point-source control for silica-containing dusts that can be
generated from machinery on sites where hydraulic fracturing is
occurring. The CDC/NIOSH mini-baghouse retrofit assembly is a bolt-on
control designed to contain silica-containing respirable dusts
generated during refill operations of sand movers during hydraulic
fracturing.
In the U.S., most new oil and gas wells are hydraulically fractured
to enhance well production. Most hydraulic fracturing operations have
2-5 sand movers on-site which transfer thousands to millions of pounds
of silica sand during each stage of fracturing. While a variety of
passive and active controls are currently available (or have been
proposed) to limit release of silica-containing dusts, the CDC/NIOSH
mini-baghouse retrofit assembly was designed to fill a unique need for
a control. The retrofit to equipment can be made in the field, uses
existing energy inherent in the system and is relatively simple and
effective. CDC/NIOSH field research has shown that risks for exposure
to respirable silica arise from at least 8 points of dust generation
and that a variety of controls (engineering, administrative and
personal protective equipment) are needed to control exposures. Use of
the mini-baghouse retrofit technology is intended to limit release of
respirable silica from thief hatches on top of the sand movers,
enhancing workplace health and safety.
Potential Commercial Applications
Controlling occupational exposure to respirable crystalline
silica, particularly during work involving transfer of sand into sand
movers on hydraulic fracturing sites
In-field retrofits of currently operating heavy equipment
(e.g., sand movers)
Limiting visible dust emissions from sand moving equipment
Reducing respirable crystalline silica dust emissions to
enhance compliance with OSHA PEL for silica
Competitive Advantages
Designed for in-field retrofitting ``thief hatches'' of
existing machinery
Uses energy inherent in the pneumatic transfer of sand
Provides a passive sand-mover-mounted control for silica
release at hydraulic fracturing operations
Development Stage
In situ data available (on-site)
Prototype
Inventors: Eric J. Esswein, Michael Breitenstein, John E. Snawder,
Michael G. Gressel, Jerry L. Kratzer (all of CDC)
Publication: Esswein EJ, et al. Occupational exposures to
respirable crystalline silica during hydraulic fracturing. JJ Occup
Environ Hyg. 2013;10(7):347-56. [PMID 23679563]
Intellectual Property: HHS Reference No. E-291-2013/0--US
Application No. 13/802,265 filed 13 Mar 2013
Licensing Contact: Whitney Blair, J.D., M.P.H.; 301-435-4937;
whitney.blair@nih.gov
Viral Like Particles Based Chikungunya Vaccines
Description of Technology: Chikungunya virus (CHIKV) is mosquito-
borne alphavirus endemic in Africa, India, and Southeast Asia. In 2013
CHIKV infection has also emerged in the Caribbean and a pandemic of
CHIKV has re-emerged in the Philippines following Typhoon Haiyan.
Currently, there is no vaccine available for the prevention of CHIKV
infection and no specific therapy exists to treat the illness.
Researchers at the Vaccine Research Center (VRC) of the National
Institute of Allergy and Infectious Diseases (NIAID) have developed a
CHIKV Viral Like Particle (CHIKV VLP) vaccine based on plasmid
expression vectors encoding structural proteins of the CHIKV virus,
which gave rise to CHIKV VLPs in transfected cells. The CHIKV VLPs
consist of the core, E1 and E2 proteins and are similar in buoyant
density and morphology to replication-competent CHIKV virus.
Immunization with CHIKV VLPs elicited neutralizing antibodies against
envelope proteins from different CHIKV strains in mouse and nonhuman
primate (NHP) models. Monkeys immunized with CHIKV VLPs produced high
titer neutralizing antibodies that protected against viremia after high
dose challenge. The selected CHIKV VLP vaccine candidate, VRC-
CHKVLP059-00-VP, composed of the E1, E2, and capsid proteins from the
CHIKV strain 37997, was recently evaluated by the VRC at the NIH
Clinical Center for safety, tolerability and immunogenicity in the
clinical protocol VRC 311 (ClinicalTrials.gov NCT01489358), a
Phase I, open-label, dose escalation clinical trial. The VRC-CHKVLP059-
00-VP vaccine was highly immunogenic, safe, and well-tolerated. VRC
researchers have also developed the transient transfection
manufacturing process for CHIKV and other alphaviruses, such as
Western, Eastern and Venezuelan Equine Encephalitis (WEVEE) viruses.
Pre-clinical in vivo mouse and NHP data, Phase 1 clinical trial data
and manufacturing data are available.
Potential Commercial Applications: Chikungunya vaccines based on
viral like particles.
Competitive Advantages
There is currently no CHIKV vaccine on the market.
VRC-CHKVLP059-00-VP vaccine candidate is highly immunogenic,
safe, and well-tolerated.
Minimal containment requirements for CHIKV VLP manufacturing
because live virus production is not required.
Development Stage
In vitro data available
In vivo data available (animal)
In vivo data available (human)
Inventors: Gary J. Nabel, Wataru Akahata, Srinivas S. Rao (all of
VRC/NIAID)
[[Page 22822]]
Publications
1. Akahata W, et al. A virus-like particle vaccine for epidemic
Chikungunya virus protects non-human primates against infection. Nat
Med. 2010 Mar;16(3):334-8. [PMID 20111039]
2. Akahata W, Nabel GJ. A specific domain of the Chikungunya virus E2
protein regulates particle formation in human cells: implications for
alphavirus vaccine design. J Virol. 2012 Aug;86(16):8879-83. [PMID
22647698]
3. Chang et al. Chikungunya Virus-Like Particle Vaccine Elicits
Neutralizing Antibodies in Healthy Adults in a Phase I Clinical Trial;
manuscript submitted.
Intellectual Property
HHS Reference Nos. E-004-2009/0/1/2--
--US Provisional Application No. 61/118,206 filed 26 Nov 2008
--US Provisional Application No. 61/201,118 filed 05 Dec 2008
--International Application No. PCT/US2009/006294 (WO 2010/062396)
filed 24 Nov 2009
--and corresponding filings in the US, Europe, China, Australia,
Brazil, India, Malaysia, South Africa, Singapore, Indonesia,
Philippines and Vietnam
HHS Reference No. E-057-2011/0/1/2--
--US Provisional Application No. 61/438,236 filed 31 Jan 2011
--International Application No. PCT/US2012/023361 (WO 2012/106356)
filed 31 Jan 2012
--and corresponding filings in the US and India
Licensing Contact: Cristina Thalhammer-Reyero, Ph.D., MBA; 301-435-
4507; ThalhamC@mail.nih.gov
Dated: April 21, 2014.
Richard U. Rodriguez,
Director, Division of Technology Development and Transfer, Office of
Technology Transfer, National Institutes of Health.
[FR Doc. 2014-09354 Filed 4-23-14; 8:45 am]
BILLING CODE 4140-01-P