1 / 5

Update from the Office of Vaccines Research and Review, CBER/FDA

Update from the Office of Vaccines Research and Review, CBER/FDA. NVAC Meeting Washington, D.C. February 4-5, 2003. New Approvals since October 2002 NVAC Meeting. FDA licensed a new combination vaccine containing DTaP, hepatitis B, and IPV in 12/02 Marketed as Pediarix â„¢ by GSK

sonel
Download Presentation

Update from the Office of Vaccines Research and Review, CBER/FDA

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Update from the Office of Vaccines Research and Review, CBER/FDA NVAC Meeting Washington, D.C. February 4-5, 2003

  2. New Approvals since October 2002 NVAC Meeting • FDA licensed a new combination vaccine containing DTaP, hepatitis B, and IPV in 12/02 • Marketed as Pediarix™ by GSK • DTaP and hepatitis B components from GSK previously licensed, but not the IPV • Indicated for active immunization against diphtheria, tetanus, pertussis, hepatitis B, and polio types 1-3 in infants born to HB-sAg negative mothers

  3. New Approvals since October 2002 (cont.) • Pediarix™ recommended for administration at 2, 4, and 6 months of age • Induced immune responses comparable to those induced by separately administered licensed vaccines • Most frequent adverse reactions: injection site reactions, fever, and fussiness • Fever occurred more frequently after administration of Pediarix™, compared with separately administered vaccines

  4. New Approvals since October 2002 (cont.) • October 2002: supplement to Wyeth’s BLA for Dryvax smallpox vaccine approved • Provides for 100-dose kit with new source of diluent and needles • January 2003: supplement to Aventis Pasteur Inc.’s BLA for DT vaccine approved • Provides for trace-thimerosal formulation

  5. VRBPAC Update • BLA for FluMist, MedImmune’s live, influenza virus vaccine discussed at Dec. 2002 VRBPAC • Majority of the committee voted that the data were adequate to support safety and effectiveness in healthy individuals 5-49 years of age • Review ongoing • Next VRBPAC meeting Feb. 20, 2003 to discuss the influenza virus strains to be included in 2003-2004 vaccine formulation

More Related