Walter A. Orenstein, M.D. Professor of Medicine and Pediatrics Director, Emory Vaccine Policy and Development Associate Director, Emory Vaccine Center

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Could Vaccines be a Possible Model For Pediatric Drug Development? June 13, 2006 Walter A. Orenstein, M.D. Professor of Medicine and Pediatrics Director, Emory Vaccine Policy and Development Associate Director, Emory Vaccine Center

Comparison of 20 th Century Annual Morbidity and Current Morbidity, Vaccine-Preventable Diseases Disease Smallpox 20th Century Annual Morbidity 48,164 2005** 0 Percent Decrease 100* Diphtheria 175,885 0 100* Measles 503,282 62 99.99 Mumps 152,209 265 99.83 Pertussis 147,271 21,003 85.74 Polio (paralytic) 16,316 1 99.99 Rubella 47,745 16 99.97 Congenital Rubella Syndrome 823 1 99.88 Tetanus 1,314 20 98.48* H. influenzae, type b and unknown (<5 yrs 20,000 199 99.01 Record lows ** Provisional Email: Barry Sirotkin 2/14/06

Diseases Prevented by Vaccination of Children 1986 2006 Diphtheria Tetanus Pertussis Polio Measles Mumps Rubella Hib Diphtheria Tetanus Pertussis Polio Measles Mumps Rubella Hib Hepatitis B Varicella Pneumococcal Disease Influenza Meningococcal Disease Rotavirus Hepatitis A Human Papillomavirus

Major New Vaccines Licensed for Universal Vaccination of Children Between 2000 and May 24, 2006 Vaccine HPV Rotavirus MMRV Tdap MCV4 LAIV DTaP-HepB HepB-IPV PCV7 Year 2006 2006 2005 2005 2005 2003 2002 2000 Manufacturers Merck Merck Merck GSK, sanofi sanofi MedImmune GSK Wyeth Excludes labeling changes, newer versions of same products, and new licenses for similar products already licensed. Source: www.fda.gov/cber/products.htm

Factors that May Influence Development of Vaccines for Children - I Large population covered universal vaccination recommendation includes at least one birth cohort annually Recommending bodies, Advisory Committee on Immunization Practices (ACIP) and American Academy of Pediatrics Committee on Infectious Diseases set standard of care Vaccines are folded into routine well clinic visits

From: http://www.cdc.gov/nip/recs/child-schedule-image1-ppt.jpg

Factors that May Influence Development of Vaccines for Children - II Vaccinations often offer protection to individual and through herd immunity to community as well Many vaccines are eventually mandated through school and/or day care laws National Vaccine Injury Compensation Program Funded by excise tax Table-related injuries Proof of causation for others There are no manufacturers of generic vaccines

Immunization Coverage Among Children 19-35 months of age, United States, 2004 Vaccines DTP-3 DTP-4 Polio-3 MMR-1 Hib-3 HepB-3 Var-1 PCV-3 Combined Series excluding PCV-3 Median age 27 months. Children Born February 2001-May2003 Coverage (%) 95.9% 85.5% 91.6% 93.0% 93.5% 92.4% 87.5% 73.2% 76.0% Source: http://www.cdc.gov/nip/coverage/nis/04/tab03_antigen_state.xls. Accessed 5/24/06

Safety Monitoring for Vaccines - I Vaccine Adverse Event Reporting System (VAERS) Passive reporting Certain adverse events required by law to be reported Stimulated through Vaccine Information Statements mandated by law for vaccines in Injury Compensation Program Maintained by FDA and CDC De-identified data available to public

Safety Monitoring for Vaccines - II Vaccine Safety Datalink (VSD) 7 HMO s; 8 plans Allows calculation of rates of adverse events Allows calculation of expected rates in absence of vaccination Allows calculation of expected rates at reference intervals before or after vaccination

Similarities Between Drug and Vaccine Development Both covered by the Pediatric Research Equity Act Requirements for licensure similar Vaccines and drugs often tested first in adults usually in Phase I settings before doing evaluations in children. Children are a vulnerable population and cannot give their own informed consent Testing in adults may provide some evidence of benefit and safety

Example of the Use of the Pediatric Research Equity Act (PREA) with Vaccines Letter from Norman W. Baylor, PhD, Director, Office of Vaccine Research and Review, 8/31/05 to GlaxoSmithKline Biologicals on Approval of Fluarix All applications for new active ingredients, new dosage forms, new indications, new routes of administration, and new dosing regimens are required to contain an assessment of the safety and effectiveness of the product in pediatric patients unless this requirement is waived or deferred. We have reviewed your submission dated May 25, 2005 and agree that a deferral of your pediatric studies for Fluarix in children <18 years of age is justified as you are pursuing with due diligence a pediatric indication for Fluarix. Source: http://www.fda.gov/cber/approvltr/inflgla083105l.htm. Accessed 5/24/06

Differences Between Drug and Vaccine Development Exclusivity has not been important in vaccine development Limited numbers of children impacted by many drugs in contrast to relatively large number of children impacted by a vaccine recommendation Vaccines often developed with childhood indication in mind. Many of the infectious diseases occur primarily in children Vaccines usually given to well children in contrast to drugs

Acknowledgments Michael Katz, March of Dimes Therese Cvetkovich,, FDA Karen Goldenthal,, FDA