Interagency Coordinating Committee on the Validation of Alternative Methods Biennial Progress Report: 2016-2017; Availability of Report, 38717-38718 [2018-16837]
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hindered both its characterization and
its use as a vaccine antigen.
Researchers at the Vaccine Research
Center (VRC) of the National Institute of
Allergy and Infectious Diseases have
overcome technical obstacles to produce
a homogeneous, soluble RSV F
glycoprotein vaccine which is stabilized
in the prefusion conformation and has
improved stability and immunogenicity
compared to the native protein.
Additionally, several modifications
were introduced to remove the
requirement for furin during
production, resulting in an increase in
expression levels of the immunogen.
Stability of the immunogen was
increased 20-fold as compared to DS–
CAV1 (a prefusion-stabilized RSV F
glycoprotein vaccine candidate that is
currently being assessed in clinical
trials) upon incubation at 60 °C. In mice,
these immunogens elicited
neutralization titers that were 2 to 5-fold
higher than DS–CAV1.
This technology is available for
licensing for commercial development
in accordance with 35 U.S.C. 209 and 37
CFR part 404, as well as for further
development and evaluation under a
research collaboration.
Potential Commercial Applications:
• Vaccine: RSV vaccine for human
use.
• Probe: B cell-sorting probe to isolate
potent neutralizing monoclonal
antibodies.
• Diagnostics: To assess the titer of
prefusion-specific antibodies in sera.
Competitive Advantages:
• Increased stability compared to the
current leading RSV vaccine candidate
(DS-Cav1).
• Elicits increased neutralization
titers in mice.
Development Stage:
• In vivo testing (mice).
Inventors: Peter D. Kwong (NIAID), M.
Gordon Joyce (NIAID), Baoshan Zhang
(NIAID), Man Chen (NIAID), Barney S.
Graham (NIAID), John R. Mascola
(NIAID), Aliaksandr A. Druz (NIAID),
Wing-Pui Kong (NIAID), Ivelin Georgiev
(NIAID), Yaroslav Tsybovsky (Leidos
Biomedical Research), Paul V. Thomas
(NIAID), Marie L. Pancera (NIAID),
Mallika Sastry (NIAID), Cinque Soto
(NIAID), Guillaume B.E. Stewart-Jones
(NIAID), Yongping Yang (NIAID), Li Ou
(NIAID), Ulrich Baxa (NCI), Emily
Rundlet (NIAID), Joseph Van Galen
(NIAID).
Publications: Joyce, M. Gordon, et al.,
Nature structural & molecular biology,
23.9 (2016): 811; PMID: 27478931.
Intellectual Property: HHS Reference
Number E–064–2016: U.S. Patent
Application No. 62/314,946 filed 03/29/
2016; PCT Application Number PCT/
VerDate Sep<11>2014
16:54 Aug 06, 2018
Jkt 244001
US2017/024714 filed 03/29/2017
(pending).
Related Intellectual Property: HHS
Reference Number E–081–2013.
Licensing Contact: Vince Contreras,
Ph.D., 240–669–2823; vince.contreras@
nih.gov.
Dated: July 20, 2018.
Suzanne M. Frisbie,
Deputy Director, Technology Transfer and
Intellectual Property Office, National Institute
of Allergy and Infectious Diseases.
[FR Doc. 2018–16835 Filed 8–6–18; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Interagency Coordinating Committee
on the Validation of Alternative
Methods Biennial Progress Report:
2016–2017; Availability of Report
AGENCY:
National Institutes of Health,
HHS.
ACTION:
Notice.
The National Toxicology
Program (NTP) Interagency Center for
the Evaluation of Alternative
Toxicological Methods (NICEATM)
announces availability of the
Interagency Coordinating Committee on
the Validation of Alternative Methods
(ICCVAM) Biennial Progress Report:
2016–2017. This report, prepared in
accordance with requirements of the
ICCVAM Authorization Act of 2000,
describes activities and
accomplishments from January 2016
through December 2017.
ADDRESSES: The report is available at
https://ntp.niehs.nih.gov/iccvamreport/
2017/.
FOR FURTHER INFORMATION CONTACT: Dr.
Warren Casey, Director, NICEATM;
email: warren.casey@nih.gov; telephone:
(984) 287–3118.
SUPPLEMENTARY INFORMATION:
Background: The ICCVAM
Authorization Act of 2000 established
ICCVAM as a permanent interagency
committee of the National Institute of
Environmental Health Sciences (NIEHS)
under NICEATM. ICCVAM’s mission is
to facilitate development, validation,
and regulatory acceptance of new and
revised regulatory test methods that
reduce, refine, or replace the use of
animals in testing while maintaining
and promoting scientific quality and the
protection of human health, animal
health, and the environment.
A provision of the ICCVAM
Authorization Act states that ICCVAM
shall prepare ‘‘reports to be made
SUMMARY:
PO 00000
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Fmt 4703
Sfmt 4703
38717
available to the public on its progress
under this Act.’’ The eighth ICCVAM
biennial progress report describing
ICCVAM activities and
accomplishments from January 2016
through December 2017 is now
available.
Summary of Report Contents: Key
ICCVAM, ICCVAM agency, and
NICEATM accomplishments
summarized in the report include:
• Development of a strategic roadmap
for incorporating new approaches into
safety testing of chemicals and medical
products in the United States.
• Publication of two guidance
documents by the U.S. Environmental
Protection Agency (EPA) in 2016. One
included a policy statement to waive all
acute dermal lethality studies for
pesticide formulations. The other
described a transparent, stepwise
process for evaluating and
implementing alternative methods for
six-pack studies, which test for acute
systemic toxicity by the oral, dermal,
and inhalation routes; skin and eye
irritation; and skin sensitization.
• Publication of notices permitting
removal of back-titration hamsters for
potency testing of vaccines containing
Leptospira pomona and Leptospira
grippotyphosa by the U.S. Department
of Agriculture, further reducing the
number of hamsters required for
leptospirosis vaccine potency testing.
• Publication by the U.S. Food and
Drug Administration of the Predictive
Toxicology Roadmap for integrating
predictive toxicology methods into
safety and risk assessments.
• Development by NICEATM and
EPA scientists of a defined approach
that combines data from 11 highthroughput screening assays with a
computational model to identify
chemicals with the potential to interact
with the androgen receptor pathway.
• Development by NICEATM and
ICCVAM scientists of a defined
approach that uses non-animal
approaches to predict murine local
lymph node assay outcomes and human
skin sensitization hazard and potency.
• Submission of a proposal to
develop a performance-based test
guideline for defined approaches to skin
sensitization testing and assessment to
the Organisation for Economic Cooperation and Development (OECD) by
partners in the International
Cooperation on Alternative Test
Methods in 2016. The proposal was
approved as part of the OECD workplan
in 2017.
• Launch of the Integrated Chemical
Environment, a publicly accessible
online resource developed to provide
high-quality curated data and
E:\FR\FM\07AUN1.SGM
07AUN1
38718
Federal Register / Vol. 83, No. 152 / Tuesday, August 7, 2018 / Notices
daltland on DSKBBV9HB2PROD with NOTICES
computational workflows to facilitate
chemical safety assessment, by
NICEATM.
Availability of Report: The report is
available at https://ntp.niehs.nih.gov/
iccvamreport/2017/. Links to
this report and all past ICCVAM annual
and biennial reports are available at
https://ntp.niehs.nih.gov/go/iccvam-bien.
Background Information on ICCVAM
and NICEATM: ICCVAM is an
interagency committee composed of
representatives from 16 federal
regulatory and research agencies that
require, use, generate, or disseminate
toxicological and safety testing
information. ICCVAM conducts
technical evaluations of new, revised,
and alternative safety testing methods
and integrated testing strategies with
regulatory applicability. ICCVAM also
promotes the scientific validation and
regulatory acceptance of testing
methods that more accurately assess the
safety and hazards of chemicals and
products and replace, reduce, or refine
(enhance animal well-being and lessen
or avoid pain and distress) animal use.
The ICCVAM Authorization Act of
2000 (42 U.S.C. 285l–3) establishes
ICCVAM as a permanent interagency
committee of NIEHS and provides the
authority for ICCVAM involvement in
activities relevant to the development of
alternative test methods. Additional
information about ICCVAM can be
found at https://ntp.niehs.nih.gov/go/
iccvam.
NICEATM administers ICCVAM,
provides scientific and operational
support for ICCVAM-related activities,
and conducts and publishes analyses
and evaluations of data from new,
revised, and alternative testing
approaches. NICEATM and ICCVAM
work collaboratively to evaluate new
and improved testing approaches
applicable to the needs of U.S. federal
agencies. NICEATM and ICCVAM
welcome the public nomination of new,
revised, and alternative testing
approaches for validation studies and
technical evaluations. Additional
information about NICEATM can be
found at https://ntp.niehs.nih.gov/go/
niceatm.
Dated: July 24, 2018.
Brian R. Berridge,
Associate Director, National Toxicology
Program.
[FR Doc. 2018–16837 Filed 8–6–18; 8:45 am]
BILLING CODE 4140–01–P
VerDate Sep<11>2014
16:54 Aug 06, 2018
Jkt 244001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of Diabetes and
Digestive and Kidney Diseases Notice
of Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended, notice is hereby given of
meetings of the National Diabetes and
Digestive and Kidney Diseases Advisory
Council.
The meetings 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 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: National Diabetes and
Digestive and Kidney Diseases Advisory
Council.
Date: September 7, 2018.
Open: 8:30 a.m. to 12:00 p.m.
Agenda: To present the Director’s Report
and other scientific presentations.
Place: National Institutes of Health,
Building 31, C Wing, 6th Floor, Conference
Room 10, 31 Center Drive, Bethesda, MD
20892.
Closed: 1:00 p.m. to 4:30 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health,
Building 31, C Wing, 6th Floor, Conference
Room 10, 31 Center Drive, Bethesda, MD
20892.
Contact Person: Karl F. Malik, Ph.D.,
Acting Director, Division of Extramural
Activities, National Institutes of Diabetes and
Digestive and Kidney Diseases, 6707
Democracy Blvd., Room 7329, MSC 5452,
Bethesda, MD 20892, (301) 594–4757,
malikk@niddk.nih.gov.
Name of Committee: National Diabetes and
Digestive and Kidney Diseases Advisory
Council; Kidney, Urologic and Hematologic
Diseases Subcommittee.
Date: September 7, 2018.
Open: 1:00 p.m. to 2:45 p.m.
Agenda: To review the Division’s scientific
and planning activities.
Place: National Institutes of Health,
Building 31, C Wing, 6th Floor, Conference
PO 00000
Frm 00042
Fmt 4703
Sfmt 4703
Room 7, 31 Center Drive, Bethesda, MD
20892.
Closed: 2:45 p.m. to 3:15 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health,
Building 31, C Wing, 6th Floor, Conference
Room 7, 31 Center Drive, Bethesda, MD
20892.
Contact Person: Karl F. Malik, Ph.D.,
Acting Director, Division Of Extramural
Activities, National Institutes of Diabetes and
Digestive and Kidney Diseases, 6707
Democracy Blvd., Room 7329, MSC 5452,
Bethesda, MD 20892, (301) 594–4757,
malikk@niddk.nih.gov.
Name of Committee: National Diabetes and
Digestive and Kidney Diseases Advisory
Council; Diabetes, Endocrinology, and
Metabolic Diseases Subcommittee.
Date: September 7, 2018.
Open: 1:00 p.m. to 2:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health,
Building 31, C Wing, 6th Floor, Conference
Room 10, 31 Center Drive, Bethesda, MD
20892.
Closed: 2:00 p.m. to 3:15 p.m.
Agenda: To review the Division’s scientific
and planning activities.
Place: National Institutes of Health,
Building 31, C Wing, 6th Floor, Conference
Room 10, 31 Center Drive, Bethesda, MD
20892.
Contact Person: Karl F. Malik, Ph.D.,
Acting Director, Division Of Extramural
Activities, National Institutes of Diabetes and
Digestive and Kidney Diseases, 6707
Democracy Blvd., Room 7329, MSC 5452,
Bethesda, MD 20892, (301) 594–4757,
malikk@niddk.nih.gov.
Name of Committee: National Diabetes and
Digestive and Kidney Diseases Advisory
Council; Digestive Diseases and Nutrition
Subcommittee.
Date: September 7, 2018.
Open: 1:00 p.m. to 2:00 p.m.
Agenda: To review the Division’s scientific
and planning activities.
Place: National Institutes of Health,
Building 31, C Wing, 6th Floor, Conference
Room 6, 31 Center Drive, Bethesda, MD
20892.
Closed: 2:15 p.m. to 3:15 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health,
Building 31, C Wing, 6th Floor, Conference
Room 6, 31 Center Drive, Bethesda, MD
20892.
Contact Person: Karl F. Malik, Ph.D.,
Acting Director, Division of Extramural
Activities, National Institutes of Diabetes and
Digestive and Kidney Diseases, 6707
Democracy Blvd., Room 7329, MSC 5452,
Bethesda, MD 20892, (301) 594–4757,
malikk@niddk.nih.gov.
Any interested person may file written
comments with the committee by forwarding
the statement to the Contact Person listed on
this notice. The statement should include the
name, address, telephone number and when
applicable, the business or professional
affiliation of the interested person.
E:\FR\FM\07AUN1.SGM
07AUN1
Agencies
[Federal Register Volume 83, Number 152 (Tuesday, August 7, 2018)]
[Notices]
[Pages 38717-38718]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-16837]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Interagency Coordinating Committee on the Validation of
Alternative Methods Biennial Progress Report: 2016-2017; Availability
of Report
AGENCY: National Institutes of Health, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The National Toxicology Program (NTP) Interagency Center for
the Evaluation of Alternative Toxicological Methods (NICEATM) announces
availability of the Interagency Coordinating Committee on the
Validation of Alternative Methods (ICCVAM) Biennial Progress Report:
2016-2017. This report, prepared in accordance with requirements of the
ICCVAM Authorization Act of 2000, describes activities and
accomplishments from January 2016 through December 2017.
ADDRESSES: The report is available at https://ntp.niehs.nih.gov/iccvamreport/2017/.
FOR FURTHER INFORMATION CONTACT: Dr. Warren Casey, Director, NICEATM;
email: [email protected]; telephone: (984) 287-3118.
SUPPLEMENTARY INFORMATION:
Background: The ICCVAM Authorization Act of 2000 established ICCVAM
as a permanent interagency committee of the National Institute of
Environmental Health Sciences (NIEHS) under NICEATM. ICCVAM's mission
is to facilitate development, validation, and regulatory acceptance of
new and revised regulatory test methods that reduce, refine, or replace
the use of animals in testing while maintaining and promoting
scientific quality and the protection of human health, animal health,
and the environment.
A provision of the ICCVAM Authorization Act states that ICCVAM
shall prepare ``reports to be made available to the public on its
progress under this Act.'' The eighth ICCVAM biennial progress report
describing ICCVAM activities and accomplishments from January 2016
through December 2017 is now available.
Summary of Report Contents: Key ICCVAM, ICCVAM agency, and NICEATM
accomplishments summarized in the report include:
Development of a strategic roadmap for incorporating new
approaches into safety testing of chemicals and medical products in the
United States.
Publication of two guidance documents by the U.S.
Environmental Protection Agency (EPA) in 2016. One included a policy
statement to waive all acute dermal lethality studies for pesticide
formulations. The other described a transparent, stepwise process for
evaluating and implementing alternative methods for six-pack studies,
which test for acute systemic toxicity by the oral, dermal, and
inhalation routes; skin and eye irritation; and skin sensitization.
Publication of notices permitting removal of back-
titration hamsters for potency testing of vaccines containing
Leptospira pomona and Leptospira grippotyphosa by the U.S. Department
of Agriculture, further reducing the number of hamsters required for
leptospirosis vaccine potency testing.
Publication by the U.S. Food and Drug Administration of
the Predictive Toxicology Roadmap for integrating predictive toxicology
methods into safety and risk assessments.
Development by NICEATM and EPA scientists of a defined
approach that combines data from 11 high-throughput screening assays
with a computational model to identify chemicals with the potential to
interact with the androgen receptor pathway.
Development by NICEATM and ICCVAM scientists of a defined
approach that uses non-animal approaches to predict murine local lymph
node assay outcomes and human skin sensitization hazard and potency.
Submission of a proposal to develop a performance-based
test guideline for defined approaches to skin sensitization testing and
assessment to the Organisation for Economic Co-operation and
Development (OECD) by partners in the International Cooperation on
Alternative Test Methods in 2016. The proposal was approved as part of
the OECD workplan in 2017.
Launch of the Integrated Chemical Environment, a publicly
accessible online resource developed to provide high-quality curated
data and
[[Page 38718]]
computational workflows to facilitate chemical safety assessment, by
NICEATM.
Availability of Report: The report is available at https://ntp.niehs.nih.gov/iccvamreport/2017/. Links to this report
and all past ICCVAM annual and biennial reports are available at https://ntp.niehs.nih.gov/go/iccvam-bien.
Background Information on ICCVAM and NICEATM: ICCVAM is an
interagency committee composed of representatives from 16 federal
regulatory and research agencies that require, use, generate, or
disseminate toxicological and safety testing information. ICCVAM
conducts technical evaluations of new, revised, and alternative safety
testing methods and integrated testing strategies with regulatory
applicability. ICCVAM also promotes the scientific validation and
regulatory acceptance of testing methods that more accurately assess
the safety and hazards of chemicals and products and replace, reduce,
or refine (enhance animal well-being and lessen or avoid pain and
distress) animal use.
The ICCVAM Authorization Act of 2000 (42 U.S.C. 285l-3) establishes
ICCVAM as a permanent interagency committee of NIEHS and provides the
authority for ICCVAM involvement in activities relevant to the
development of alternative test methods. Additional information about
ICCVAM can be found at https://ntp.niehs.nih.gov/go/iccvam.
NICEATM administers ICCVAM, provides scientific and operational
support for ICCVAM-related activities, and conducts and publishes
analyses and evaluations of data from new, revised, and alternative
testing approaches. NICEATM and ICCVAM work collaboratively to evaluate
new and improved testing approaches applicable to the needs of U.S.
federal agencies. NICEATM and ICCVAM welcome the public nomination of
new, revised, and alternative testing approaches for validation studies
and technical evaluations. Additional information about NICEATM can be
found at https://ntp.niehs.nih.gov/go/niceatm.
Dated: July 24, 2018.
Brian R. Berridge,
Associate Director, National Toxicology Program.
[FR Doc. 2018-16837 Filed 8-6-18; 8:45 am]
BILLING CODE 4140-01-P