96-22485. Advisory Committee; Notice of Meeting  

  • [Federal Register Volume 61, Number 172 (Wednesday, September 4, 1996)]
    [Notices]
    [Pages 46652-46653]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 96-22485]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
    
    Advisory Committee; Notice of Meeting
    
    AGENCY: Food and Drug Administration, HHS.
    
    ACTION: Notice.
    
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    SUMMARY: This notice announces a forthcoming meeting of a public 
    advisory committee of the Food and Drug Administration (FDA). This 
    notice also summarizes the procedures for the meeting 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.
    
    MEETING: The following advisory committee meeting is announced:
    
    
    Antiviral Drugs Advisory Committee
    
        Date, time, and place. September 26, 1996, 1 p.m. and September 27, 
    1996, 8:30 a.m., Holiday Inn--Gaithersburg, Goshen Ballroom, Two 
    Montgomery Village Ave., Gaithersburg, MD.
        Type of meeting and contact person. Open committee discussion, 
    September 26, 1996, 1 p.m. to 3 p.m.; open public hearing, 3 p.m. to 
    3:30 p.m., unless public participation does not last that long; open 
    committee discussion, 3:30 p.m. to 5 p.m.; open committee discussion, 
    September 27, 1996, 8:30 a.m. to 11 a.m.; open public hearing, 11 a.m. 
    to 12 m., unless public participation does not last that long; open 
    committee discussion, 12 m. to 4:30 p.m.; Rhonda W. Stover, Center for
    
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    Drug Evaluation and Research (HFD-21), Food and Drug Administration, 
    5600 Fishers Lane, Rockville, MD 20857, 301-443-5455, or FDA Advisory 
    Committee Information Hotline, 1-800-741-8138 (301-443-0572 in the 
    Washington, DC area), Antiviral Drugs Advisory Committee, code 12531. 
    Please call the hotline for information concerning any possible 
    changes.
        General functions of the committee. The committee reviews and 
    evaluates available data concerning the safety and effectiveness of 
    marketed and investigational human drug products for use in the 
    treatment of acquired immune deficiency syndrome (AIDS), AIDS-related 
    complex (ARC), and other viral, fungal, and mycobacterial infections.
        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 September 20, 1996, 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 September 26, 1996, the committee 
    will discuss data relevant to the approved drug, saquinavir 
    (InviraseTM, Hoffmann-La Roche), for use in combination with 
    nucleoside analogues for the treatment of human immunodeficiency virus 
    (HIV) infection. On September 27, 1996, the committee will discuss data 
    relevant to new drug application 20-705, delavirdine 
    (Rescriptor, Pharmacia and Upjohn Co.) for use in the 
    treatment of HIV infection.
        FDA public advisory committee meetings 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. 
    There are no closed portions for the meetings announced in this notice. 
    The dates and times reserved for the open 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, 5600 Fishers Lane, rm. 12A-16, 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, 12420 Parklawn Dr., rm. 1-23, 
    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.
        This notice is issued under section 10(a)(1) and (a)(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: August 27, 1996.
    Michael A. Friedman,
    Deputy Commissioner for Operations.
    [FR Doc. 96-22485 Filed 9-3-96; 8:45 am]
    BILLING CODE 4160-01-F
    
    
    

Document Information

Published:
09/04/1996
Department:
Health and Human Services Department
Entry Type:
Notice
Action:
Notice.
Document Number:
96-22485
Pages:
46652-46653 (2 pages)
PDF File:
96-22485.pdf