Oncologic Drugs Advisory Committee; Notice of Meeting, 62482-62483 [E7-21630]
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62482
Federal Register / Vol. 72, No. 213 / Monday, November 5, 2007 / Notices
directed toward adolescent age groups;
and
• Discuss other potential future
actions to promote safe and effective use
of OTC drugs by adolescents.
IV. Workshop Attendance and
Registration
The Natcher Conference Center is a
Federal facility with security procedures
for entrance. Workshop attendees will
be required to show proper
identification and are asked to allow
ample time to enter the NIH campus.
There is no fee to attend the
workshop, and attendees who do not
wish to make an oral presentation do
not need to register. Seating will be on
a first-come, first-served basis.
If you would like to make an oral
presentation during the workshop, you
must register by close of business on
November 21, 2007. You must provide
your name, title, business affiliation (if
applicable), address, and type of
organization you represent (e.g.,
industry, consumer organization) to Lee
Lemley or Faith Dugan at 301–594–6779
(see FOR FURTHER INFORMATION CONTACT).
Persons registered to make an oral
presentation should check in before the
workshop.
If you need special accommodations
because of disability, please contact Lee
Lemley (see FOR FURTHER INFORMATION
CONTACT) at least 7 days before the
workshop.
V. Comments
Interested persons may submit to the
Division of Dockets Management (see
ADDRESSES) written or electronic
comments regarding the issues and
questions presented in this document.
Submit a single copy of electronic
comments or two paper copies of any
mailed comments, except that
individuals may submit one paper copy.
Comments are to be identified with the
docket number found in brackets in the
heading of this document. Received
comments may be seen in the Division
of Dockets Management between 9 a.m.
and 4 p.m., Monday through Friday.
ycherry on PRODPC74 with NOTICES
VI. Workshop Transcripts
We will prepare a transcript of the
workshop. The transcript will be
available for review approximately 30
days after the workshop at the Division
of Dockets Management (see ADDRESSES)
between 9 a.m. and 4 p.m., Monday
through Friday. The transcript will also
be available on the Internet at https://
www.fda.gov/ohrms/dockets.
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Dated: October 30, 2007.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E7–21713 Filed 11–2–07; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
Oncologic Drugs Advisory Committee;
Notice of Meeting
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
This notice announces a forthcoming
meeting of a public advisory committee
of the Food and Drug Administration
(FDA). At least one portion of the
meeting will be closed to the public.
Name of Committee: Oncologic Drugs
Advisory Committee.
General Function of the Committee:
To provide advice and
recommendations to the agency on
FDA’s regulatory issues.
Date and Time: The meeting will be
held on December 5, 2007, from 8 a.m.
to 5 p.m.
Location: Hilton Washington DC
North/Gaithersburg, The Ballrooms, 620
Perry Pkwy., Gaithersburg, MD. The
hotel phone number is 301–977–8900.
Contact Person: Nicole Vesely, 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, 301–827–6793, FAX: 301–
827–6776, e-mail:
nicole.vesely@fda.hhs.gov, or FDA
Advisory Committee Information Line,
1–800–741–8138 (301–443–0572 in the
Washington, DC area), code
3014512542. Please call the Information
Line for up-to-date information on this
meeting. A notice in the Federal
Register about last minute modifications
that impact a previously announced
advisory committee meeting cannot
always be published quickly enough to
provide timely notice. Therefore, you
should always check the agency’s Web
site and call the appropriate advisory
committee hot line/phone line to learn
about possible modifications before
coming to the meeting.
Agenda: On December 5, 2007, from
8 a.m. to 3 p.m., the committee will
discuss supplemental biologics license
application (sBLA) 125085/91,
AVASTIN (bevacizumab), Genentech,
Inc., proposed indication, in
combination with paclitaxel, for the
treatment of patients who have not
PO 00000
Frm 00055
Fmt 4703
Sfmt 4703
received chemotherapy for their locally
recurrent or metastatic, HER2 negative
breast cancer. From 3:30 p.m. to 5 p.m.,
the committee will meet in closed
session.
FDA intends to make background
material available to the public no later
than 2 business days before the meeting.
If FDA is unable to post the background
material on its Web site prior to the
meeting, the background material will
be made publicly available at the
location of the advisory committee
meeting, and the background material
will be posted on FDA’s Web site after
the meeting. Background material is
available at https://www.fda.gov/ohrms/
dockets/ac/acmenu.htm, click on the
year 2007 and scroll down to the
appropriate advisory committee link.
Procedure: On December 5, 2007,
from 8 a.m. to 3 p.m., the meeting is
open to the public. Interested persons
may present data, information, or views,
orally or in writing, on issues pending
before the committee. Written
submissions may be made to the contact
person on or before November 21, 2007.
Oral presentations from the public will
be scheduled between approximately 11
a.m. and 12 noon. Those desiring to
make formal oral presentations should
notify the contact person and submit a
brief statement of the general nature of
the evidence or arguments they wish to
present, the names and addresses of
proposed participants, and an
indication of the approximate time
requested to make their presentation on
or before November 13, 2007. Time
allotted for each presentation may be
limited. If the number of registrants
requesting to speak is greater than can
be reasonably accommodated during the
scheduled open public hearing session,
FDA may conduct a lottery to determine
the speakers for the scheduled open
public hearing session. The contact
person will notify interested persons
regarding their request to speak by
November 14, 2007.
Closed Committee Deliberations: On
December 5, 2007, from 3:30 p.m. to 5
p.m., the meeting will be closed to
permit discussion and review of trade
secret and/or confidential information
(5 U.S.C. 552b(c)(4)). During this
session, the committee will be briefed
on recent and upcoming applications
within the Office of Oncology Products.
Persons attending FDA’s advisory
committee meetings are advised that the
agency is not responsible for providing
access to electrical outlets.
FDA welcomes the attendance of the
public at its advisory committee
meetings and will make every effort to
accommodate persons with physical
disabilities or special needs. If you
E:\FR\FM\05NON1.SGM
05NON1
Federal Register / Vol. 72, No. 213 / Monday, November 5, 2007 / Notices
require special accommodations due to
a disability, please contact Nicole
Vesely at least 7 days in advance of the
meeting.
FDA is committed to the orderly
conduct of its advisory committee
meetings. Please visit our Web site at
https://www.fda.gov/oc/advisory/
default.htm for procedures on public
conduct during advisory committee
meetings.
Notice of this meeting is given under
the Federal Advisory Committee Act (5
U.S.C. app. 2).
Dated: October 24, 2007.
Randall W. Lutter,
Deputy Commissioner for Policy.
[FR Doc. E7–21630 Filed 11–2–07; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Cooperative Agreement for Poison
Prevention Education; CFDA #93.253
Health Resources and Services
Administration (HRSA), HHS.
ACTION: Notice of Single Source Award.
AGENCY:
Stabilization and Enhancement Grant
Program.
Project Period: The period of the
award is from September 1, 2007,
through April 1, 2008.
Justification for the Exception to
Competition
This project will be implemented
through a single source cooperative
agreement because the HSC is uniquely
positioned to immediately undertake
and complete the activities within the
seven month time frame. HSC is
currently developing low literacy
poison prevention materials, and this
project will enhance the existing
package of materials. The HSC has
existing organizational knowledge and
experience in developing materials for
the low literacy population through its
Home Safety Literacy Project, of which
this project will be a component. The
HSC has an existing relationship with
key stakeholders in place for reaching
this vulnerable population, and the HSC
project director has extensive expertise
in poison prevention education.
Dated: October 26, 2007.
Dennis P. Williams,
Deputy Administrator.
[FR Doc. E7–21677 Filed 11–2–07; 8:45 am]
HRSA will be enhancing the
partnership with the Home Safety
Council (HSC) to collaborate on
reaching America’s low literacy
population. Through this project,
additional poison prevention training
materials targeting the low literacy
population will be developed and
distributed to the public, poison centers,
safety and injury prevention
professionals, health educators, and first
responders. HRSA first announced the
partnership with the HSC in the Federal
Register, Vol. 71, No. 146, July 31, 2006.
FOR FURTHER INFORMATION CONTACT: Lori
Roche, Director, Poison Control
Program, Healthcare Systems Bureau,
Room 11C–06, 5600 Fishers Lane,
Rockville, MD 20857; Telephone: 301–
443–0652; E-mail: lroche@hrsa.gov.
SUPPLEMENTARY INFORMATION:
Intended Recipient of the Award:
Home Safety Council.
Amount of the Award: $75,000.
BILLING CODE 4165–15–P
Authority: Section 1271 et seq. of the
Public Health Service Act, 42 U.S.C. 300d–
71 et seq. as amended by the Poison Center
The National Survey on Drug Use and
Health (NSDUH), formerly the National
Household Survey on Drug Abuse
ycherry on PRODPC74 with NOTICES
SUMMARY:
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Substance Abuse and Mental Health
Services Administration
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Periodically, the Substance Abuse and
Mental Health Services Administration
(SAMHSA) will publish a summary of
information collection requests under
OMB review, in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
documents, call the SAMHSA Reports
Clearance Officer on (240) 276–1243.
Project: 2008–2010 National Survey on
Drug Use and Health: Methodological
Field Tests—NEW
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62483
(NHSDA), is a survey of the civilian,
non-institutionalized population of the
United States 12 years old and older.
The data are used to determine the
prevalence of use of tobacco products,
alcohol, illicit substances, and illicit use
of prescription drugs. The results are
used by SAMHSA, ONDCP, Federal
government agencies, and other
organizations and researchers to
establish policy, direct program
activities, and better allocate resources.
This will be a request for generic
approval for information collection for
NSDUH methodological field tests
designed to examine the feasibility,
quality, and efficiency of new
procedures of revisions to the existing
survey protocol. These field tests will
examine ways to increase data quality,
lower operating costs, and gain a better
understanding of various sources of
nonsampling error. If these tests provide
successful results, current procedures
may be revised and incorporated into
the main study (e.g., questionnaire
changes). Particular attention will be
given to minimizing the impact of
design changes so that survey data
continue to remain comparable over
time.
Field test activities are expected to
include improving response rates among
persons residing in controlled access
communities (locked apartment
buildings, gated communities, college
dormitories, etc.), and conducting a
nonresponse follow-up study. Cognitive
laboratory testing will be conducted
prior to the implementation of
significant questionnaire modifications.
These questionnaire modifications will
also be pre-tested and the feasibility of
text-to-speech software determined. To
understand the effectiveness of current
monetary incentive, a new incentive
study will be conducted with varying
incentive amounts. The relationship
between incentives and veracity of
reporting will also be examined. Tests
will also be designed to determine the
feasibility of alternative sample designs
and modes of data collection. Lastly, a
customer satisfaction survey of NSDUH
data users will be conducted to improve
the utility of the NSDUH data. Some of
the above studies may be combined to
introduce survey efficiencies.
The average annual burden associated
with these activities over a three-year
period is summarized below:
E:\FR\FM\05NON1.SGM
05NON1
Agencies
[Federal Register Volume 72, Number 213 (Monday, November 5, 2007)]
[Notices]
[Pages 62482-62483]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-21630]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
Oncologic Drugs Advisory Committee; Notice of Meeting
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
This notice announces a forthcoming meeting of a public advisory
committee of the Food and Drug Administration (FDA). At least one
portion of the meeting will be closed to the public.
Name of Committee: Oncologic Drugs Advisory Committee.
General Function of the Committee: To provide advice and
recommendations to the agency on FDA's regulatory issues.
Date and Time: The meeting will be held on December 5, 2007, from 8
a.m. to 5 p.m.
Location: Hilton Washington DC North/Gaithersburg, The Ballrooms,
620 Perry Pkwy., Gaithersburg, MD. The hotel phone number is 301-977-
8900.
Contact Person: Nicole Vesely, 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, 301-827-6793, FAX: 301-827-6776, e-mail:
nicole.vesely@fda.hhs.gov, or FDA Advisory Committee Information Line,
1-800-741-8138 (301-443-0572 in the Washington, DC area), code
3014512542. Please call the Information Line for up-to-date information
on this meeting. A notice in the Federal Register about last minute
modifications that impact a previously announced advisory committee
meeting cannot always be published quickly enough to provide timely
notice. Therefore, you should always check the agency's Web site and
call the appropriate advisory committee hot line/phone line to learn
about possible modifications before coming to the meeting.
Agenda: On December 5, 2007, from 8 a.m. to 3 p.m., the committee
will discuss supplemental biologics license application (sBLA) 125085/
91, AVASTIN (bevacizumab), Genentech, Inc., proposed indication, in
combination with paclitaxel, for the treatment of patients who have not
received chemotherapy for their locally recurrent or metastatic, HER2
negative breast cancer. From 3:30 p.m. to 5 p.m., the committee will
meet in closed session.
FDA intends to make background material available to the public no
later than 2 business days before the meeting. If FDA is unable to post
the background material on its Web site prior to the meeting, the
background material will be made publicly available at the location of
the advisory committee meeting, and the background material will be
posted on FDA's Web site after the meeting. Background material is
available at https://www.fda.gov/ohrms/dockets/ac/acmenu.htm, click on
the year 2007 and scroll down to the appropriate advisory committee
link.
Procedure: On December 5, 2007, from 8 a.m. to 3 p.m., the meeting
is open to the public. Interested persons may present data,
information, or views, orally or in writing, on issues pending before
the committee. Written submissions may be made to the contact person on
or before November 21, 2007. Oral presentations from the public will be
scheduled between approximately 11 a.m. and 12 noon. Those desiring to
make formal oral presentations should notify the contact person and
submit a brief statement of the general nature of the evidence or
arguments they wish to present, the names and addresses of proposed
participants, and an indication of the approximate time requested to
make their presentation on or before November 13, 2007. Time allotted
for each presentation may be limited. If the number of registrants
requesting to speak is greater than can be reasonably accommodated
during the scheduled open public hearing session, FDA may conduct a
lottery to determine the speakers for the scheduled open public hearing
session. The contact person will notify interested persons regarding
their request to speak by November 14, 2007.
Closed Committee Deliberations: On December 5, 2007, from 3:30 p.m.
to 5 p.m., the meeting will be closed to permit discussion and review
of trade secret and/or confidential information (5 U.S.C. 552b(c)(4)).
During this session, the committee will be briefed on recent and
upcoming applications within the Office of Oncology Products.
Persons attending FDA's advisory committee meetings are advised
that the agency is not responsible for providing access to electrical
outlets.
FDA welcomes the attendance of the public at its advisory committee
meetings and will make every effort to accommodate persons with
physical disabilities or special needs. If you
[[Page 62483]]
require special accommodations due to a disability, please contact
Nicole Vesely at least 7 days in advance of the meeting.
FDA is committed to the orderly conduct of its advisory committee
meetings. Please visit our Web site at https://www.fda.gov/oc/advisory/
default.htm for procedures on public conduct during advisory committee
meetings.
Notice of this meeting is given under the Federal Advisory
Committee Act (5 U.S.C. app. 2).
Dated: October 24, 2007.
Randall W. Lutter,
Deputy Commissioner for Policy.
[FR Doc. E7-21630 Filed 11-2-07; 8:45 am]
BILLING CODE 4160-01-S