Attach 2 60 day FRN

72206

Federal Register / Vol. 76, No. 225 / Tuesday, November 22, 2011 / Notices

1. Samuel T. Sicard, individually and
as trustee of the Samuel M. Sicard
Living Trust, Fort Smith, Arkansas; to
retain ownership of First Bank Corp.,
and thereby indirectly retain ownership
of The First National Bank of Fort
Smith, both in Fort Smith, Arkansas.
Board of Governors of the Federal Reserve
System, November 17, 2011.
Robert deV. Frierson,
Deputy Secretary of the Board.

Board of Governors of the Federal Reserve
System, November 17, 2011.
Robert deV. Frierson,
Deputy Secretary of the Board.

[FR Doc. 2011–30106 Filed 11–21–11; 8:45 am]
BILLING CODE 6210–01–P

FEDERAL RESERVE SYSTEM

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Omni Bank, National Association,
Alhambra, California.
In connection with this application,
Applicants also have applied to retain
5.9 percent interest of the voting shares
of First PacTrust Bancorp, Inc., and
thereby indirectly retain Pacific Trust
Bank, both in Chula Vista, California,
and engage in operating as savings and
loan association, pursuant to section
225.28(b)(4)(ii) of Regulation Y.

[FR Doc. 2011–30105 Filed 11–21–11; 8:45 am]

Formations of, Acquisitions by, and
Mergers of Bank Holding Companies

BILLING CODE 6210–01–P

The companies listed in this notice
have applied to the Board for approval,
pursuant to the Bank Holding Company
Act of 1956 (12 U.S.C. 1841 et seq.)
(BHC Act), Regulation Y (12 CFR Part
225), and all other applicable statutes
and regulations to become a bank
holding company and/or to acquire the
assets or the ownership of, control of, or
the power to vote shares of a bank or
bank holding company and all of the
banks and nonbanking companies
owned by the bank holding company,
including the companies listed below.
The applications listed below, as well
as other related filings required by the
Board, are available for immediate
inspection at the Federal Reserve Bank
indicated. The application also will be
available for inspection at the offices of
the Board of Governors. Interested
persons may express their views in
writing on the standards enumerated in
the BHC Act (12 U.S.C. 1842(c)). If the
proposal also involves the acquisition of
a nonbanking company, the review also
includes whether the acquisition of the
nonbanking company complies with the
standards in section 4 of the BHC Act
(12 U.S.C. 1843). Unless otherwise
noted, nonbanking activities will be
conducted throughout the United States.
Unless otherwise noted, comments
regarding each of these applications
must be received at the Reserve Bank
indicated or the offices of the Board of
Governors not later than December 16,
2011.
A. Federal Reserve Bank of San
Francisco (Kenneth Binning, Vice
President, Applications and
Enforcement) 101 Market Street, San
Francisco, California 94105–1579:
1. American Start-Up Financial
Institutions Investments, I, L.P., and
CKH Capital, Inc., both in Monterey
Park, California; to become bank
holding companies by acquiring up to
62 percent of the voting shares of New

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

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Centers for Disease Control and
Prevention
[60Day–12–12AM]

Proposed Data Collections Submitted
for Public Comment and
Recommendations
In compliance with the requirement
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for
opportunity for public comment on
proposed data collection projects, the
Centers for Disease Control and
Prevention (CDC) will publish periodic
summaries of proposed projects. To
request more information on the
proposed projects or to obtain a copy of
the data collection plans and
instruments, call (404) 639–5960 and
send comments to Daniel Holcomb, CDC
Reports Clearance Officer, 1600 Clifton
Road, MS–D74, Atlanta, GA 30333 or
send an email to [email protected].
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; and (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology. Written comments should
be received within 60 days of this
notice.
Proposed Project
Prospective Birth Cohort Study
Involving Environmental Uranium

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Exposure in the Navajo Nation (U01)—
New—National Center for
Environmental Health (NCEH) and
Agency for Toxic Substances and
Disease Registry (ATSDR), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The Navajo Nation includes 16
million acres of New Mexico, Utah and
Arizona. It is the largest Alaska Native/
American Indian Reservation in the
United States. From 1948 to 1986, many
uranium mining and milling operations
took place in the Navajo Nation, leaving
a large amount of uranium
contamination on the reservation.
Several studies have reported that
uranium mostly damages the kidneys
and urinary system. However, there is
not much research data on uranium
exposure and poor birth and
reproductive health outcomes. Research
involving prenatal exposure to uranium
may help to understand and prevent
some unfavorable child and maternal
health outcomes.
There are important health differences
concerning birth outcomes and prenatal
care in the Navajo Nation. According to
the Indian Health Service Regional
Differences in Indian Health 2002–2003
Edition, the infant death rate among the
Navajo people is 8.5 deaths per 1000
live births, compared to 6.9 deaths per
1000 live births among all races. Only
61% of Navajo mothers with live births
received prenatal care in the first
trimester as compared to 83% of all U.S.
mothers. Early and regular prenatal care
is a major predicator of positive birth
outcomes. Due to the health differences
in birth outcomes and the chance for
environmental uranium exposure in the
Navajo Nation, ATSDR decided that the
upcoming study must include education
of women and their families about the
importance of prenatal care and the
potential poor health risks associated
with exposure to uranium.
The House Committee on Oversight
and Government Reform requested that
federal agencies develop a plan to
address health and environmental
impacts of uranium contamination in
the Navajo Nation. As a result of this
request, ATSDR awarded a research
cooperative agreement to University of
New Mexico Community Environmental
Health Program (UNM–CEHP) entitled
‘‘A Prospective Birth Cohort Study
Involving Environmental Uranium
Exposure in the Navajo Nation (U01),’’
in August 2010. ATSDR and UNM–
CEHP are working with the Navajo Area
Indian Health Service (NAIHS), Navajo
Nation Division of Health (NNDOH),
Navajo Nation Environmental Protection
Agency (NNEPA), and Navajo culture

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72207

Federal Register / Vol. 76, No. 225 / Tuesday, November 22, 2011 / Notices
and language specialists to carry out the
study. The study will examine
reproductive outcomes in pregnant
women, follow and assess their children
from birth to 1 year of age, and create
a system to follow up the infants
through childhood up to 6 years of age
to evaluate the impact of uranium
exposure on biological and psychosocial
endpoints. Biological sample analysis,
surveys, and developmental screenings
will be performed during this research
period for each participant.
In addition to investigating the role of
uranium and other chemicals in the
environment on birth outcomes and
development, the prospective study may
aid in understanding causes and
prevention measures of chronic
conditions. Several research studies
have shown that exposure to chemicals
in the environment during prenatal and
postnatal periods can affect the
development of adult chronic diseases.
The study will also provide broad
public health benefits for Navajo
communities through outreach and
education on environmental prenatal
risks and early assessment. Referrals
will also be provided for known
developmental delays.

enrollment survey for fathers who agree
to participate will also be administered.
Community Health and Environmental
Research Specialists (CHERS) will
administer surveys using a CDCapproved electronic data entry system.
Survey instruments were designed to
collect demographic information, assess
potential environmental health risks,
and mother-child interactions. The
survey instruments were developed
based on previous surveys conducted by
Dine’ Network for Environmental Health
(DiNEH) Project, the National Children’s
Study, and by other birth cohort studies
that have been conducted among other
indigenous populations. The final
format of the survey instruments was
modified based on review and input
from the Navajo Nation community
liaison group and associated Navajo
staff to address issues such as cultural
sensitivity, comprehension and
language translation.
There is no cost to the respondents
other than their time to participate in
the study. The total estimated annual
burden hours equals 3550.
Estimated Annualized Burden Hours

Number of respondents

Number of responses per
respondent

550
500

1
4

2
15/60

1100
500

500
500
500

1
1
4

15/60
1
15/60

125
500
500

Father ...........................................

Enrollment Survey .................................
Ages and Stages Questionnaire (2,6,9
12 months).
Mullen Stages of Early Development ....
Postpartum Survey (0 months) .............
Post-partum Survey (2, 6, 9, 12
months).
Enrollment Survey .................................

550

1

90/60

825

Total ......................................

................................................................

........................

........................

........................

3550

Type of respondent

Form name

Mother ..........................................

Dated: November 16, 2011.
Daniel Holcomb,
Reports Clearance Officer, Centers for Disease
Control and Prevention.
[FR Doc. 2011–30103 Filed 11–21–11; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

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

SUMMARY:

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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.
ADDRESSES:

National Institutes of Health

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Participants will include Native
American mothers from age 14 to 45
with verification of pregnancy who have
lived in the study area for at least 5
years. Also, participants must consent to
receive prenatal care and deliver at one
of the healthcare facilities that are
taking part in the study (Northern
Navajo Medical Center, Chinle
Comprehensive Health Care Facility,
Gallup Indian Medical Center, Tuba
City Regional Health-Care Corporation,
or Tse´hootsooı´ Medical Center). Fathers
will be included in the study with
consent regardless of age or residence.
We estimate that 550 pregnant women
and fathers per year must be enrolled in
the study to obtain adequate statistical
power. A 10% pregnancy loss will be
assumed, which would result in 500
live births per year. Therefore, the total
anticipated sample size is 1,500 motherinfant pairs over the three years of the
study.
The survey instruments for pregnant
mothers include the following:
Enrollment Survey, Nutritional
Assessment/Food Intake Questionnaire,
Ages and Stages Questionnaire (ASQ–I),
Mullen Stages of Early Development
(MSEL), and Postpartum Surveys. An

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Average burden response
(hours)

Total burden
(hours)

Medical Device for Intraocular
Injection of Therapeutics and Fluid
Sampling
Description of Technology: The
National Institutes of Health seeks
research collaboration and
commercialization partners for a
medical device for administering
therapeutics into the eye to treat a
variety of ocular diseases including
diabetic retinopathy, retinal vein
occlusion, and macular degeneration.
The device is a dual function needle
that can both inject and sample ocular
fluid at the same injection site. The
needle includes a hub portion in
communication with a needle portion
through a lumen that may be used as a
conduit to inject a therapeutic into an
injection site. A sample chamber, with
an optional absorbent material, is

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