[Federal Register Volume 78, Number 95 (Thursday, May 16, 2013)]
[Notices]
[Pages 28866-28867]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2013-11693]
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DEPARTMENT OF HOMELAND SECURITY
[Docket No. DHS-2013-0036]
Cooperative Research and Development Agreement (CRADA)
Opportunity With the Department of Homeland Security for the
Development of a Foot-and-Mouth Disease 3ABC ELISA Diagnostic Kit
AGENCY: Science and Technology Directorate, Plum Island Animal Disease
Center, Department of Homeland Security.
ACTION: Notice of intent.
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SUMMARY: The Department of Homeland Security Science and Technology
Directorate (DHS S&T), through its Plum Island Animal Disease Center
(PIADC), is seeking industry collaborators to aid DHS S&T in developing
an ELISA diagnostic test that it capable of obtaining a U.S. regulatory
license to detect antibodies to at least one of the Foot and Mouth
Disease virus (FMDV) non-structural proteins (NSP): 3A, 3B, or 3C. This
new FMDV 3ABC ELISA may be used in the event of a real or suspected
outbreak of Foot-and-Mouth Disease (FMD) in order to differentiate
infected from vaccinated, non-infected animals (DIVA).
The role of the industry collaborator(s) in this CRADA will be to
develop and validate the FMDV 3ABC ELISA assay in collaboration with
DHS S&T and the United States Department of Agriculture Animal and
Plant Health Inspection Service Foreign Animal Disease Diagnostic
Laboratory (USDA APHIS FADDL) at PIADC, and with other U.S.
laboratories that are associated with USDA, such as the National Animal
Health Laboratory Network (NAHLN). Components of a prototype assay,
developed by USDA, Texas Veterinary Medical Diagnostic Laboratory, and
a 3rd party fee-for-service contractor, will be made available to the
industry collaborator(s). The goal of the CRADA is to submit a data
package to USDA APHIS Center for Veterinary Biologics (CVB) in order to
obtain a U.S. regulatory license for use under the direction of USDA
administrators of the FMDV 3ABC ELISA in the U.S. (See CVB Veterinary
Services Memorandum No. 800.73 for ``General Requirements for
Immunodiagnostic Test Kits for the Detection of Antibody or Antigen.'')
The assay must also successfully identify and test a reference panel of
sera provided by OIE (World Organisation for Animal Health) as tested
in a U.S. Reference Laboratory, e.g., USDA APHIS FADDL.
DHS S&T is seeking CRADA collaborators that own or have access to
the technological components for, have the technological expertise in,
and have proven track records of success in the fields of diagnostic
test kit research, development, and the obtaining of USDA licensure for
the detection of antibodies to viral antigen(s). CRADA collaborators
must indicate if they are currently or may be funded by the Federal
government, and, if yes, they must include a discussion of how proposed
CRADA work and Federal government-funded work would not be duplicative.
The proposed term of the CRADA can be up to thirty (30) months.
DATES: Submit comments on or before June 17, 2013.
ADDRESSES: Mail comments and requests to participate to Dr. Angela
Ervin, (ATTN: Angela Ervin, 245 Murray Lane SW., Washington, DC 20528-
0075). Submit electronic comments and other data to
[email protected].
FOR FURTHER INFORMATION CONTACT:
Information on DHS CRADAs: Marlene Owens, (202) 254-6671.
SUPPLEMENTARY INFORMATION:
Assay Requirements
1. Ideally a competitive ELISA (an assay in which a molecule in the
test sample competes against a reagent provided in the kit for binding
to the target) for FMDV NSPs that will differentiate FMDV infected from
FMDV vaccinated animals (DIVA) (specifically cattle) and can be made
commercially by the CRADA partner or by another entity and upon request
by USDA APHIS, be supplied to USDA APHIS FADDL and accredited state
laboratories within the National Animal Health Laboratory Network.
2. The ideal assay will have the following characteristics:
a. Diagnostic sensitivity of at least 96% for all seven major
serotypes of FMDV, including detection of cattle antibodies to FMDV
within 7 to 10 days post-infection.
b. Diagnostic specificity of at least 96%, ideally >99% with
respect to viruses that cause FMDV look-alike clinical signs, such as
Vesicular Stomatitis Virus, Swine Vesicular Disease Virus, Bovine
Rhinovirus, Seneca Valley Virus.
c. Compatibility with serum samples from U.S. national cattle (beef
and dairy) and domestic swine herds, and ideally with other species
that are susceptible to FMDV, e.g., sheep, goats, feral swine, buffalo,
deer, antelope, etc.
[[Page 28867]]
d. Assay time not exceeding 4 hours from start of incubation to
beginning of reading the plate.
e. 96 well modular format.
f. Positive control (produced from non-FMDV infected animals, e.g.,
hyperimmunized with synthetically made FMDV peptides/proteins) and
negative control (produced from na[iuml]ve animals) for each plate.
g. Compatibility with Biosafety Level 2 (BSL-2) laboratory
requirements, i.e., will not contain any reagents considered to be
select agents or potentially contaminated with select agents.
3. Transportability under cold chain (1) to USDA APHIS PIADC, (2)
upon USDA APHIS administrator request approved laboratories within the
National Animal Health Laboratory network, and (3) outside of the US
without special restrictions.
DHS S&T Role (includes but not limited to)
1. As necessary, coordination of development and commercialization
access to critical assay components such as the recombinant 3ABC*
protein (* indicates that the 3C protein has a mutation in the active
site) and a FMDV-specific monoclonal antibody, which may be negotiated
through intellectual property licenses with 3rd parties who control
rights to these assay components. DHS will supply data from testing a
prototype assay, but DHS will not supply historical background or any
proprietary information.
2. Coordination of testing and evaluation of samples from U.S.
cattle and swine vaccinated with FMD molecular vaccines.
3. Coordination of testing and evaluation of true positive samples
from U.S. cattle and swine that were experimentally infected. A maximum
of 500 samples can be tested.
4. If requested, coordination of testing and evaluation of true
positive and true negative samples from other FMDV susceptible U.S.
domestic species.
5. If requested, coordination of testing and evaluation of serum
samples from FMDV susceptible U.S. wildlife species.
6. The actual testing of samples listed above mainly by scientists
in USDA APHIS FADDL or by partners in laboratories that USDA APHIS
FADDL and DHS S&T will identify, e.g., the NAHLN.
Period of Performance
If CRADA collaborator(s) is (are) selected, a comprehensive data
package to obtain a USDA license for the FMDV 3ABC ELISA for use in
cattle should be submitted to USDA APHIS CVB within 30 months of the
CRADA award date. The submission must adhere to the requirements in
USDA APHIS CVB Veterinary Services Memo No. 800.73 and other applicable
CVB 9CFR requirements for diagnostic kits and reagents. The assay must
also successfully identify samples in a reference panel of sera
provided by OIE (World Organisation for Animal Health) as tested in a
U.S. reference laboratory, e.g., USDA APHIS FADDL. Because these
reference panels are provided on a yearly basis to FMD world reference
laboratories, the testing and analysis of results may extend beyond the
30 month Period of Performance. Nevertheless, results should be made
available within 2 months of the availability of reference panels.
Selection Criteria
The Plum Island Animal Disease Center (PIADC) reserves the right to
select CRADA collaborators for all, some, or none of the proposals in
response to this notice. PIADC will provide no funding for
reimbursement of proposal development costs. Proposals (or any other
material) submitted in response to this notice will not be returned.
Proposals submitted are expected to be unclassified.
PIADC will select proposals at its sole discretion on the basis of:
1. How well the proposal communicates the collaborators'
understanding of and ability to meet the CRADAs goals and proposed
timeline.
2. How well the proposal addresses the following criteria:
a. Capability of the collaborator to provide equipment and
materials for proposed testing.
b. Capability of the collaborator to meet the requirements for
development, validation testing and analysis, and submission of
supporting data and documents fulfilling the CVB requirements for
licensure in the U.S.
c. Preliminary data or results which support the assay requirements
outlined above.
Participation in this CRADA does not imply the future purchase of
any materials, equipment, or services from the collaborating entities,
and non-Federal CRADA participants will not be excluded from any future
PIADC procurements based solely on their participation in this CRADA.
Authority: CRADAs are authorized by the Federal Technology
Transfer Act of 1986, as amended and codified by 15 U.S.C. 3710a.
DHS, as an executive agency under 5 U.S.C. 105, is a Federal agency
for the purposes of 15 U.S.C. 3710a and may enter into a CRADA. DHS
delegated the authority to conduct CRADAs to the Science and
Technology Directorate and its laboratories.
Dated: May 9, 2013.
James Johnson,
Director, Office of National Laboratories.
[FR Doc. 2013-11693 Filed 5-15-13; 8:45 am]
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