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U.S. Department of Health and Human Services

Advisory Committees

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December 8, 2009: Meeting of the Pediatric Advisory Committee Meeting Announcement (Amended as of October 30)

CenterDateTimeLocation
OCDecember 8, 2009
 
8:00 a.m. - 6:00 p.m.
 
Hilton, WashingtonDC/Rockville Executive Meeting Center, 1750 Rockville Pike, Rockville, Maryland, 20852

Agenda

On December 8, 2009, the Pediatric Advisory Committee will meet to discuss pediatric-focused safety reviews, as mandated by the Best Pharmaceuticals for Children Act and the Pediatric Research Equity Act, for Abilify (aripiprazole), Argatroban (argatroban), Orencia (abatacept), Humira (adalimumab), Cancidas (caspofungin acetate), Evicel - fibrin sealant (human), Artiss - fibrin sealant (human), Voluven - 6% hydroxyethyl starch 130/0.4 in 0.9% sodium chloride injection, Reyataz (atazanavir sulfate), Kaletra (lopinavir/ ritonavir), Aptivus (tipranavir), Zetia (ezetimibe), Vytorin (ezetimibe/simvastatin), Ventolin HFA (albuterol sulfate). An update to address some of the committee’s questions from the November 18th, 2008 Pediatric Advisory Committee meeting on atypical antipsychotic drugs will be provided. In addition to Abilify (aripiprazole), Risperidal (risperidone), Zyprexa (olanzapine), Geodon (ziprasidone), and Seroquel (quetiapine) will be included.


 

Meeting Materials

FDA intends to make the complete 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.


 

 

Public Participation and Sponsor Information Interested persons and Sponsors (representatives from industry) 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 24, 2009. Comments received on or before December 5, 2009, will be provided to
  • Oral presentations from the public (excluding Sponsors) will be scheduled between approximately 1 p.m. and 2 p.m on December 8, 2009. 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 16, 2009. 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 17, 2009.

 

Contact Information

  • Doreen Kezer, MSN
    Office of Science and Public Health
    Office of the Commissioner (HF–33)
    Food and Drug Administration
    5600 Fishers Lane (for express delivery, rm. 14–65)
    Rockville, MD 20857
    Phone: 301–827–1249
    Fax: 301-827-3042
    E-mail: doreen.kezer@fda.hhs.gov
  • FDA Advisory Committee Information Line 1-800-741-8138
    (301-443-0572 in the Washington DC area) Code:8732310001
    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.

 

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.

 

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 require special accommodations due to a disability, please contact Doreen Kezer, MSN at (301) 827-1249 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 http://www.fda.gov/AdvisoryCommittees/AboutAdvisoryCommittees
/ucm111462.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).