Proposed Data Collection; Comment Request; California Health Interview Survey 2007, 51833-51834 [06-7328]
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Federal Register / Vol. 71, No. 169 / Thursday, August 31, 2006 / Notices
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Joan E. Ohl,
Commissioner, Administration on Children,
Youth and Families.
[FR Doc. 06–7364 Filed 8–30–06; 8:45 am]
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Dated: August 25, 2006.
Randall W. Lutter,
Associate Commissioner for Policy and
Planning.
[FR Doc. 06–7310 Filed 8–30–06; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
Anti-Infective Drugs Advisory
Committee Meeting; Amendment of
Notice
AGENCY:
BILLING CODE 4160–01–S
Food and Drug Administration,
HHS.
ACTION:
Notice.
erjones on PROD1PC72 with NOTICES
15:29 Aug 30, 2006
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
The Food and Drug
Administration (FDA) is announcing an
amendment to the notice of a meeting of
the Anti-Infective Drugs Advisory
Committee. This meeting was
announced in the Federal Register of
July 25, 2006 (71 FR 42096). The
amendment is being made to reflect a
change in the Date and Time and
Agenda portions of the document. The
meeting scheduled for September 11,
2006, has been cancelled. There are no
other changes.
FOR FURTHER INFORMATION CONTACT:
Sohail Mosaddegh, Center for Drug
Evaluation and Research (HFD–21),
Food and Drug Administration, 5600
Fishers Lane (for express delivery, 5630
Fishers Lane, rm. 1093), Rockville, MD
20857, 301–827–7001, FAX: 301–827–
6776, e-mail:
sohail.mosaddegh@fda.hhs.gov, or FDA
Advisory Committee Information Line,
1–800–741–8138 (301–443–0572 in the
Washington DC area), code 3014512530.
Please call the Information Line for upto-date information on this meeting.
SUPPLEMENTARY INFORMATION: In the
Federal Register of July 25, 2006 (71 FR
42096), FDA announced that a meeting
of the Anti-Infective Drugs would be
held on September 11 and 12, 2006. On
page 42096, in the second column, the
Date and Time portion of the meeting is
amended to read as follows:
Date and Time: The meeting will held
on September 12, 2006, from 8 a.m. to
5 p.m.
On page 42096, third column, the
Agenda portion of the meeting is
amended to read as follows:
Agenda: On September 12, 2006, the
committee will discuss supplemental
SUMMARY:
VerDate Aug<31>2005
new drug application (sNDA) 21–158/S–
006, FACTIVE (gemifloxacin mesylate)
Tablets, submitted by Oscient
Pharmaceuticals Corp., for the proposed
treatment of acute baterial sinusitis.
This notice is issued under the
Federal Advisory Committee Act (5
U.S.C. app. 2) and 21 CFR part 14,
relating to advisory committees.
Jkt 208001
Proposed Data Collection; Comment
Request; California Health Interview
Survey 2007
SUMMARY: 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,
National Cancer Institute (NCI), the
National Institute of Health (NIH) will
publish periodic summaries of proposed
projects to be submitted to the Office of
Management and Budget (OMB) for
review and approval.
The first California Health Interview
Survey (CHIS) Cancer Control Module
(CCM) took place in 2001 (2000 CHIS
CCM, OMB No. 0925–0478, Federal
Register, May 8, 2000, Vol. 65, No. 89,
p. 26620). The second survey took place
in 2003 (2003 CHIS CCM, OMB No.
0925–0518, Federal Register, October 3,
2002, Volume 67, No. 192, pp. 62067–
62068) and the third in 2005 (2005 CHIS
CCM, OMB No. 0925–0000, Federal
Register, Vol. 69, No. 150, Aug. 5, 2004,
pp. 47450–47451, and Federal Register,
Vol. 70, No. 1, Jan. 3, 2005, pp. 93–94).
Proposed Collection
Title: California Health Interview
Survey (CHIS) 2007 Cancer Control
Module (CCM). Type of Information
Collection Request: New. Need and Use
of Information Collection: The NCI has
sponsored three Cancer Control
Modules in the California Health
Interview Survey (CHIS), and will be
sponsoring a fourth to be administered
in 2007.
The CHIS is a telephone survey
designed to provide population-based,
PO 00000
Frm 00037
Fmt 4703
Sfmt 4703
51833
standardized health-related data to
assess California’s progress in meeting
Healthy People 2010 objectives for the
nation and the state. The CHIS sample
is designed to provide statistically
reliable estimates statewide, for
California counties, and for California’s
ethnically and racially diverse
population. Initiated by the UCLA
Center for Health Policy Research, the
California Department of Health
Services, and the California Public
Health Institute, the survey is funded by
a number of public and private sources.
It was first administered in 2001 to
55,428 adults and subsequently in 2003
and 2005 to 42,043 and 43,020 adults
respectively. These adults are a
representative sample of California’s
non-institutionalized population living
in households.
CHIS 2007, the fourth bi-annual
survey, is planned for administration to
55,000 adult Californians. The cancer
control module, which is similar to that
administered in CHIS 2001, CHIS 2003,
and CHIS 2005, will allow NCI to
examine trends in breast cancer
screening and diagnosis, as well as to
study other cancer-related topics such
as diet, physical activity, and obesity.
Because California is the most
populous and the most racially and
ethnically diverse state in the nation,
the CHIS 2007 sample will yield
adequate numbers of respondents in key
ethnic and racial groups, including
African Americans, Latinos, Asians, and
American Indian/Alaska Natives. The
Latino group will include large numbers
of respondents in the Mexican, Central
American, South American, and other
Latino subgroups; the Asian group will
include large numbers of respondents in
the Chinese, Filipino, Japanese,
Vietnamese, and Korean subgroups. NCI
will compare the CHIS and National
Health Interview Survey (NHIS) data in
order to conduct comparative analyses
and better estimate cancer risk factors
and screening among racial/ethnic
minority populations. The CHIS sample
size also permits NCI to create estimates
for ethnic subdomains of the
population, for which NHIS has
insufficient numbers for analysis.
Frequency of Response: One-time.
Affected public: Individuals or
households. Types of Respondents: U.S.
adults (persons 18 years of age and
older).
The annual reporting burden is as
follows.
E:\FR\FM\31AUN1.SGM
31AUN1
51834
Federal Register / Vol. 71, No. 169 / Thursday, August 31, 2006 / Notices
TABLE A.—ANNUALIZED BURDEN ESTIMATES FOR CHIS 2007 DATA COLLECTION
Estimated
number of
respondents
Data collection
Frequency of
response
Average time
per response
Annual hour
burden
(1) Pilot Test Adult Demographics .................................................................
CCM ...............................................................................................................
(2) Full Survey Adult Demographics ..............................................................
CCM ...............................................................................................................
150
150
55,000
55,000
1
1
1
1
.07
.03
.07
.03
11
5
3,850
1,650
Totals ......................................................................................................
55,150
1
.1
5,516
There are no Capital Costs to report. There are no Operating or Maintenance Costs to report.
Request for Comments: Written
comments and/or suggestions from the
public and affected agencies are invited
on one or more of the following points:
(1) Whether the proposed collection of
information is necessary for the
proposed performance of the functions
of the agency, including whether the
information shall have practical utility;
(2) The accuracy of the agency’s
estimate of the burden of the proposed
collection of information including the
validity of the methodology and
assumptions used; (3) Ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4)
Ways to minimize the burden of the
collection of information on those who
are to respond, including the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
To
request more information on the
proposed project or to obtain a copy of
the data collection plans and
instruments, contact Nancy Breen,
Ph.D., Project Officer, National Cancer
Institute, EPN 4005, 6130 Executive
Boulevard MSC 7344, Bethesda,
Maryland 20852–7344, or call non-toll
free number 301–496–8500 or FAX your
request, including your address to
breenn@mail.nih.gov.
Comments Due Date: Comments
regarding this information collection are
best assured of having their full effect if
received within 60 days of this
publication.
FOR FURTHER INFORMATION CONTACT:
erjones on PROD1PC72 with NOTICES
Dated: August 24, 2006.
Rachelle Ragland-Greene,
NCI Project Clearance Liaison, National
Institutes of Health.
[FR Doc. 06–7328 Filed 8–30–06; 8:45 am]
BILLING CODE 4140–01–P
VerDate Aug<31>2005
15:29 Aug 30, 2006
Jkt 208001
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:
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.
ADDRESSES: 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.
Novel Acylthiol Compositions and
Methods of Making and Using Them
Description of Technology: This
invention provides a novel family of
acylthiols and uses thereof. More
specifically, this invention provides
effective inhibitors of HIV that
selectively target its highly conserved
nucleocapsid protein (NCp7) by
interacting with metal chelating
structures of a zinc finger-containing
protein. Because of the mutationally
intolerant nature of NCp7, drug
resistance is much less likely to occur
with compounds attacking this target. In
addition, these drugs should inactivate
all types and strains of HIV and could
also inactivate other retroviruses, since
most retroviruses share one or two
PO 00000
Frm 00038
Fmt 4703
Sfmt 4703
highly conserved zinc fingers that have
the CCHC motif of the HIV Ncp7.
Finally, this invention could be very
useful for the large-scale practical
synthesis of HIV inhibitors, because
these compounds can be prepared by
using inexpensive starting materials and
facile reactions. Thus, it opens the
possibility that an effective drug
treatment for HIV could be made
available to much larger populations.
These thioesters may also be used as an
active component in topical
applications that serve as a barrier to
HIV infection.
Inventors: John K. Inman (NIAID),
Atul Goel (NCI), Ettore Appella (NCI),
James A. Turpin (NIAID), Marco Schito
(NCI).
Publications:
1. ML Schito, A Goel, Y Song, JK
Inman, RJ Fattah, WG Rice, JA Turpin,
A Sher, E Appella. In vitro antiviral
activity of novel human
immunodeficiency virus type 1
nucleocapsid p7 zinc finger inhibitors
in a transgenic murine model. AIDS Res
Hum Retroviruses. 2003 Feb;19(2):91–
101.
2. P Srivastava, M Schito, RJ Fattah,
T Hara, T Hartman, RW Buckheit Jr, JA
Turpin, JK Inman, E Appella.
Optimization of unique, uncharged
thioesters as inhibitors of HIV
replication. Bioorg Med Chem. 2004 Dec
15;12(24):6437–6450.
3. LM Jenkins, JC Byrd, T Hara, P
Srivastava, SJ Mazu, SJ Stahl, JK Inman,
E Appella, JG Omichinski, P Legault.
Studies on the mechanism of
inactivation of the HIV–1 nucleocapsid
protein NCp7 with 2mercaptobenzamide thioesters. J Med
Chem. 2005 Apr 21;48(8):2847–2858.
4. V Basrur, Y Song, SJ Mazur, Y
Higashimoto, JA Turpin, WG Rice, JK
Inman, E Appella. Inactivation of HIV–
1 nucleocapsid protein P7 by
pyridinioalkanoyl thioesters.
Characterization of reaction products
and proposed mechanism of action. J
Biol Chem. 2000 May 19;275(20):14890–
14897.
5. JA Turpin, Y Song, JK Inman, M
Huang, A Wallqvist, A Maynard, DG
E:\FR\FM\31AUN1.SGM
31AUN1
Agencies
[Federal Register Volume 71, Number 169 (Thursday, August 31, 2006)]
[Notices]
[Pages 51833-51834]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 06-7328]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Proposed Data Collection; Comment Request; California Health
Interview Survey 2007
SUMMARY: 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, National Cancer Institute (NCI),
the National Institute of Health (NIH) will publish periodic summaries
of proposed projects to be submitted to the Office of Management and
Budget (OMB) for review and approval.
The first California Health Interview Survey (CHIS) Cancer Control
Module (CCM) took place in 2001 (2000 CHIS CCM, OMB No. 0925-0478,
Federal Register, May 8, 2000, Vol. 65, No. 89, p. 26620). The second
survey took place in 2003 (2003 CHIS CCM, OMB No. 0925-0518, Federal
Register, October 3, 2002, Volume 67, No. 192, pp. 62067-62068) and the
third in 2005 (2005 CHIS CCM, OMB No. 0925-0000, Federal Register, Vol.
69, No. 150, Aug. 5, 2004, pp. 47450-47451, and Federal Register, Vol.
70, No. 1, Jan. 3, 2005, pp. 93-94).
Proposed Collection
Title: California Health Interview Survey (CHIS) 2007 Cancer
Control Module (CCM). Type of Information Collection Request: New. Need
and Use of Information Collection: The NCI has sponsored three Cancer
Control Modules in the California Health Interview Survey (CHIS), and
will be sponsoring a fourth to be administered in 2007.
The CHIS is a telephone survey designed to provide population-
based, standardized health-related data to assess California's progress
in meeting Healthy People 2010 objectives for the nation and the state.
The CHIS sample is designed to provide statistically reliable estimates
statewide, for California counties, and for California's ethnically and
racially diverse population. Initiated by the UCLA Center for Health
Policy Research, the California Department of Health Services, and the
California Public Health Institute, the survey is funded by a number of
public and private sources. It was first administered in 2001 to 55,428
adults and subsequently in 2003 and 2005 to 42,043 and 43,020 adults
respectively. These adults are a representative sample of California's
non-institutionalized population living in households.
CHIS 2007, the fourth bi-annual survey, is planned for
administration to 55,000 adult Californians. The cancer control module,
which is similar to that administered in CHIS 2001, CHIS 2003, and CHIS
2005, will allow NCI to examine trends in breast cancer screening and
diagnosis, as well as to study other cancer-related topics such as
diet, physical activity, and obesity.
Because California is the most populous and the most racially and
ethnically diverse state in the nation, the CHIS 2007 sample will yield
adequate numbers of respondents in key ethnic and racial groups,
including African Americans, Latinos, Asians, and American Indian/
Alaska Natives. The Latino group will include large numbers of
respondents in the Mexican, Central American, South American, and other
Latino subgroups; the Asian group will include large numbers of
respondents in the Chinese, Filipino, Japanese, Vietnamese, and Korean
subgroups. NCI will compare the CHIS and National Health Interview
Survey (NHIS) data in order to conduct comparative analyses and better
estimate cancer risk factors and screening among racial/ethnic minority
populations. The CHIS sample size also permits NCI to create estimates
for ethnic subdomains of the population, for which NHIS has
insufficient numbers for analysis.
Frequency of Response: One-time. Affected public: Individuals or
households. Types of Respondents: U.S. adults (persons 18 years of age
and older).
The annual reporting burden is as follows.
[[Page 51834]]
Table A.--Annualized Burden Estimates for CHIS 2007 Data Collection
----------------------------------------------------------------------------------------------------------------
Estimated
Data collection number of Frequency of Average time Annual hour
respondents response per response burden
----------------------------------------------------------------------------------------------------------------
(1) Pilot Test Adult Demographics............... 150 1 .07 11
CCM............................................. 150 1 .03 5
(2) Full Survey Adult Demographics.............. 55,000 1 .07 3,850
CCM............................................. 55,000 1 .03 1,650
---------------------------------------------------------------
Totals...................................... 55,150 1 .1 5,516
----------------------------------------------------------------------------------------------------------------
There are no Capital Costs to report. There are no Operating or Maintenance Costs to report.
Request for Comments: Written comments and/or suggestions from the
public and affected agencies are invited on one or more of the
following points: (1) Whether the proposed collection of information is
necessary for the proposed performance of the functions of the agency,
including whether the information shall have practical utility; (2) The
accuracy of the agency's estimate of the burden of the proposed
collection of information including the validity of the methodology and
assumptions used; (3) Ways to enhance the quality, utility, and clarity
of the information to be collected; and (4) Ways to minimize the burden
of the collection of information on those who are to respond, including
the use of appropriate automated, electronic, mechanical, or other
technological collection techniques or other forms of information
technology.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the data collection plans and
instruments, contact Nancy Breen, Ph.D., Project Officer, National
Cancer Institute, EPN 4005, 6130 Executive Boulevard MSC 7344,
Bethesda, Maryland 20852-7344, or call non-toll free number 301-496-
8500 or FAX your request, including your address to
breenn@mail.nih.gov.
Comments Due Date: Comments regarding this information collection
are best assured of having their full effect if received within 60 days
of this publication.
Dated: August 24, 2006.
Rachelle Ragland-Greene,
NCI Project Clearance Liaison, National Institutes of Health.
[FR Doc. 06-7328 Filed 8-30-06; 8:45 am]
BILLING CODE 4140-01-P