[Federal Register Volume 60, Number 100 (Wednesday, May 24, 1995)]
[Notices]
[Pages 27530-27532]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 95-12661]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
Advisory Committees; Notice of Meetings
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces forthcoming meetings of public advisory
committees of the Food and Drug Administration (FDA). This notice also
summarizes the procedures for the meetings and methods by which
interested persons may participate in open public hearings before FDA's
advisory committees.
FDA has established an Advisory Committee Information Hotline (the
hotline) using a voice-mail telephone system. The hotline provides the
public with access to the most current information on FDA advisory
committee meetings. The advisory committee hotline, which will
disseminate current information and information updates, can be
accessed by dialing 1-800-741-8138 or 301-443-0572. Each advisory
committee is assigned a 5-digit number. This 5-digit number will appear
in each individual notice of meeting. The hotline will enable the
public to obtain information about a particular advisory committee by
using the committee's 5-digit number. Information in the hotline is
preliminary and may change before a meeting is actually held. The
hotline will be updated when such changes are made.
MEETINGS: The following advisory committee meetings are announced:
Oncologic Drugs Advisory Committee
Date, time, and place. June 8 and 9, 1995, 8 a.m., Parklawn Bldg.,
conference rooms D and E, 5600 Fishers Lane, Rockville, MD.
Type of meeting and contact person. Open public hearing, June 8,
1995, 8 a.m. to 9 a.m., unless public participation does not last that
long; open committee discussion, 9 a.m. to 5 p.m.; open committee
discussion, June 9, 1995, 8 a.m. to 11:30 a.m.; closed committee
deliberations, 11:30 a.m. to 4 p.m.; Adele S. Seifried, Center for Drug
Evaluation and Research (HFD-9), Food and Drug Administration, 5600
Fishers Lane, Rockville, MD 20857, 301-443-4695, or FDA Advisory
Committee Information Hotline, 1-800-741-8138 (301-443-0572 in the
Washington, DC area), Oncologic Drugs Advisory Committee, code 12542.
General function of the committee. The committee reviews and
evaluates data on the safety and effectiveness of marketed and
investigational human drugs for use in treatment of cancer.
Agenda--Open public hearing. Interested persons may present data,
information, or views, orally or in writing, on issues pending before
the committee. Those desiring to make formal presentations should
notify the contact person before June 5, 1995, 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 required to make their comments.
Open committee discussion. On June 8, 1995, the committee will
discuss: (1) New drug application (NDA) 50-704, Daunoxome
Injection (liposomal daunorubicin, Vestar, Inc.) ``as the primary
therapy for the palliative management of advanced, HIV-associated
Kaposi's Sarcoma,'' and (2) NDA 20-449, Taxotere (docetaxel,
Rhone-Poulenc Rorer), for treatment of ``patients with locally advanced
or metastatic breast carcinoma in whom previous therapy has failed;
prior therapy should have included an anthracycline unless clinically
contraindicated.'' On June 9, 1995, the committee will discuss NDA 20-
221, Ethyol (amifostine injection, U.S. Bioscience, Inc.) ``as a
cytoprotective agent against the cumulative renal toxicities associated
with cisplatin and the cumulative hematologic toxicity associated with
cyclophosphamide and cisplatin in patients with advanced solid tumors
of non-germ cell origin.''
Closed committee deliberations. On June 9, 1995, the committee will
discuss trade secret and/or confidential commercial information
relevant to investigational new drugs (IND's) and pending NDA's. This
portion of the meeting will be closed to permit discussion of this
information (5 U.S.C. 552b(c)(4)).
Orthopedic and Rehabilitation Devices Panel of the Medical Devices
Advisory Committee
Date, time, and place. June 12, 1995, 8:30 a.m., Holiday Inn--
Gaithersburg, Ballroom, Two Montgomery Village Ave., Gaithersburg, MD.
A limited number of overnight accommodations have been reserved at the
Holiday Inn--Gaithersburg. Attendees requiring overnight accommodations
may contact the hotel at 301-948-8900 and reference the FDA panel
meeting block. Reservations will be confirmed at the group rate based
on availability.
Type of meeting and contact person. Open public hearing, 8:30 a.m.
to 9 a.m., unless public participation does not last that long; open
committee discussion, 9 a.m. to 12 m.; closed committee deliberations,
12 m. to 1:30 p.m.; open public hearing, 1:30 p.m. to 2 p.m., unless
public participation does not last that long; open committee
discussion, 2 p.m. to 5 p.m.; Paula J. Wilkerson, [[Page 27531]] Center
for Devices and Radiological Health (HFZ-410), Food and Drug
Administration, 9200 Corporate Blvd., Rockville, MD 20850, 301-594-
2036, or FDA Advisory Committee Information Hotline, 1-800-741-8138
(301-443-0572 in the Washington, DC area), Orthopedic and
Rehabilitation Panel, code 12521.
General function of the committee. The committee reviews and
evaluates data on the safety and effectiveness of marketed and
investigational devices and makes recommendations for their regulation.
Agenda--Open public hearing. Interested persons may present data,
information, or views, orally or in writing, on issues pending before
the committee. Those desiring to make formal presentations should
notify the contact person before June 1, 1995, 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 required to make their comments.
Open committee discussion. The committee will discuss general
issues relating to a premarket approval application for a total knee
replacement device. The committee will also hear an FDA presentation on
conditions of approval and the gathering of long-term data. The
afternoon session will include presentations and committee discussion
on hip replacement systems. Speakers will examine components of
clinical protocol design including: Medical and clinical aspects,
rating systems, patient selection, controls, and statistical
considerations.
Closed committee deliberations. The committee will discuss trade
secret and/or confidential commercial information relating to
orthopedic devices. This portion of the meeting will be closed to
permit discussion of this information (5 U.S.C. 552b(c)(4)).
Blood Products Advisory Committee
Date, time, and place. June 23, 1995, 8 a.m., Marriott--Bethesda,
Congressional Salons I, II, and III, 5151 Pooks Hill Rd., Bethesda, MD.
Type of meeting and contact person. Open committee discussion, 8
a.m. to 10:45 a.m.; open public hearing, 10:45 a.m. to 11:45 a.m.,
unless public participation does not last that long; open committee
discussion, 11:45 a.m. to 3 p.m.; closed committee deliberations, 3
p.m. to 3:30 p.m.; Linda A. Smallwood, Center for Biologics Evaluation
and Research (HFM-350), Food and Drug Administration, 1401 Rockville
Pike, Rockville, MD 20852-1448, 301-594-6700, or FDA Advisory Committee
Information Hotline, 1-800-741-8138 (301-443-0572 in the Washington, DC
area), Blood Products Advisory Committee, code 12388.
General function of the committee. The committee reviews and
evaluates data on the safety and effectiveness, and appropriate use of
blood products intended for use in the diagnosis, prevention, or
treatment of human diseases.
Agenda--Open public hearing. Interested persons may present data,
information, or views, orally or in writing, on issues pending before
the committee. Those desiring to make formal presentations should
notify the contact person before June 12, 1995, 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 required to make their comments.
Open committee discussion. In the morning, the committee will
discuss and provide recommendations on human immunodeficiency virus
(HIV) antigen screening of blood donors. In the afternoon, the
committee will discuss and review the report of the intramural research
site visit of the Laboratory of Cellular Hematology, Division of
Hematology, Office of Blood Research and Review, Center for Biologics
Evaluation and Research.
Closed committee deliberations. The committee will discuss the
intramural scientific program. This portion of the meeting will be
closed to prevent disclosure of personal information concerning
individuals associated with the research program, a disclosure of which
would constitute a clearly unwarranted invasion of personal privacy (5
U.S.C. 552b(c)(6)).
Each public advisory committee meeting listed above may have as
many as four separable portions: (1) An open public hearing, (2) an
open committee discussion, (3) a closed presentation of data, and (4) a
closed committee deliberation. Every advisory committee meeting shall
have an open public hearing portion. Whether or not it also includes
any of the other three portions will depend upon the specific meeting
involved. The dates and times reserved for the separate portions of
each committee meeting are listed above.
The open public hearing portion of each meeting shall be at least 1
hour long unless public participation does not last that long. It is
emphasized, however, that the 1 hour time limit for an open public
hearing represents a minimum rather than a maximum time for public
participation, and an open public hearing may last for whatever longer
period the committee chairperson determines will facilitate the
committee's work.
Public hearings are subject to FDA's guideline (subpart C of 21 CFR
part 10) concerning the policy and procedures for electronic media
coverage of FDA's public administrative proceedings, including hearings
before public advisory committees under 21 CFR part 14. Under 21 CFR
10.205, representatives of the electronic media may be permitted,
subject to certain limitations, to videotape, film, or otherwise record
FDA's public administrative proceedings, including presentations by
participants.
Meetings of advisory committees shall be conducted, insofar as is
practical, in accordance with the agenda published in this Federal
Register notice. Changes in the agenda will be announced at the
beginning of the open portion of a meeting.
Any interested person who wishes to be assured of the right to make
an oral presentation at the open public hearing portion of a meeting
shall inform the contact person listed above, either orally or in
writing, prior to the meeting. Any person attending the hearing who
does not in advance of the meeting request an opportunity to speak will
be allowed to make an oral presentation at the hearing's conclusion, if
time permits, at the chairperson's discretion.
The agenda, the questions to be addressed by the committee, and a
current list of committee members will be available at the meeting
location on the day of the meeting.
Transcripts of the open portion of the meeting may be requested in
writing from the Freedom of Information Office (HFI-35), Food and Drug
Administration, rm. 12A-16, 5600 Fishers Lane, Rockville, MD 20857,
approximately 15 working days after the meeting, at a cost of 10 cents
per page. The transcript may be viewed at the Dockets Management Branch
(HFA-305), Food and Drug Administration, rm. 1-23, 12420 Parklawn Dr.,
Rockville, MD 20857, approximately 15 working days after the meeting,
between the hours of 9 a.m. and 4 p.m., Monday through Friday. Summary
minutes of the open portion of the meeting may be requested in writing
from the Freedom of Information Office (address above) beginning
approximately 90 days after the meeting.
The Commissioner has determined for the reasons stated that those
portions of the advisory committee meetings so designated in this
notice shall be closed. The Federal Advisory Committee Act (FACA) (5
U.S.C. app. 2, 10(d)), permits [[Page 27532]] such closed advisory
committee meetings in certain circumstances. Those portions of a
meeting designated as closed, however, shall be closed for the shortest
possible time, consistent with the intent of the cited statutes.
The FACA, as amended, provides that a portion of a meeting may be
closed where the matter for discussion involves a trade secret;
commercial or financial information that is privileged or confidential;
information of a personal nature, disclosure of which would be a
clearly unwarranted invasion of personal privacy; investigatory files
compiled for law enforcement purposes; information the premature
disclosure of which would be likely to significantly frustrate
implementation of a proposed agency action; and information in certain
other instances not generally relevant to FDA matters.
Examples of portions of FDA advisory committee meetings that
ordinarily may be closed, where necessary and in accordance with FACA
criteria, include the review, discussion, and evaluation of drafts of
regulations or guidelines or similar preexisting internal agency
documents, but only if their premature disclosure is likely to
significantly frustrate implementation of proposed agency action;
review of trade secrets and confidential commercial or financial
information submitted to the agency; consideration of matters involving
investigatory files compiled for law enforcement purposes; and review
of matters, such as personnel records or individual patient records,
where disclosure would constitute a clearly unwarranted invasion of
personal privacy.
Examples of portions of FDA advisory committee meetings that
ordinarily shall not be closed include the review, discussion, and
evaluation of general preclinical and clinical test protocols and
procedures for a class of drugs or devices; consideration of labeling
requirements for a class of marketed drugs or devices; review of data
and information on specific investigational or marketed drugs and
devices that have previously been made public; presentation of any
other data or information that is not exempt from public disclosure
pursuant to the FACA, as amended; and, deliberation to formulate advice
and recommendations to the agency on matters that do not independently
justify closing.
This notice is issued under section 10(a)(1) and (2) of the Federal
Advisory Committee Act (5 U.S.C. app. 2), and FDA's regulations (21 CFR
part 14) on advisory committees.
Dated: May 17, 1995.
Linda A. Suydam,
Interim Deputy Commissioner for Operations.
[FR Doc. 95-12661 Filed 5-23-95; 8:45 am]
BILLING CODE 4160-01-F
