TY - JOUR
T1 - Human challenge trials in vaccine development, Rockville, MD, USA, September 28–30, 2017
AU - Session chairs at the second Human Challenge Trials meeting
AU - Baay, Marc F.D.
AU - Richie, Thomas L.
AU - Neels, Pieter
AU - Cavaleri, Marco
AU - Chilengi, Roma
AU - Diemert, David
AU - Hoffman, Stephen L.
AU - Johnson, Robert
AU - Kirkpatrick, Beth D.
AU - Knezevic, Ivana
AU - Laurens, Matthew
AU - McShane, Helen
AU - Njuguna, Patricia
AU - Older Aguilar, Anastazia
AU - Pollard, Andrew J.
AU - Riddle, Mark
AU - Sauerwein, Robert
AU - Southern, James
AU - Tribble, David
AU - Wildfire, Adrian
N1 - Publisher Copyright:
© 2018
PY - 2019/9
Y1 - 2019/9
N2 - The International Alliance for Biological Standardization organized the second workshop on human challenge trials (HCT) in Rockville, MD, in September 2017. The objective of this meeting was to examine the use of HCT, in response to the continuing human suffering caused by infectious diseases, preventable by the development of new and improved vaccines. For this, the approach of HCT could be valuable, as HCT can provide key safety, tolerability, immunogenicity, and efficacy data, and can be used to study host-pathogen biology. HCT can generate these data with speed, efficiency and minimal expense, albeit not with the same level of robustness as clinical trials. Incorporated wisely into a clinical development plan, HCT can support optimization or down-selection of new vaccine candidates, assuring that only the worthiest candidates progress to field testing. HCT may also provide pivotal efficacy data in support of licensure, particularly when field efficacy studies are not feasible. Many aspects of HCT were discussed by the participants, including new and existing models, standardization and ethics. A consensus was achieved that HCT, if ethically justified and performed with careful attention to safety and informed consent, should be pursued to promote and accelerate vaccine development.
AB - The International Alliance for Biological Standardization organized the second workshop on human challenge trials (HCT) in Rockville, MD, in September 2017. The objective of this meeting was to examine the use of HCT, in response to the continuing human suffering caused by infectious diseases, preventable by the development of new and improved vaccines. For this, the approach of HCT could be valuable, as HCT can provide key safety, tolerability, immunogenicity, and efficacy data, and can be used to study host-pathogen biology. HCT can generate these data with speed, efficiency and minimal expense, albeit not with the same level of robustness as clinical trials. Incorporated wisely into a clinical development plan, HCT can support optimization or down-selection of new vaccine candidates, assuring that only the worthiest candidates progress to field testing. HCT may also provide pivotal efficacy data in support of licensure, particularly when field efficacy studies are not feasible. Many aspects of HCT were discussed by the participants, including new and existing models, standardization and ethics. A consensus was achieved that HCT, if ethically justified and performed with careful attention to safety and informed consent, should be pursued to promote and accelerate vaccine development.
KW - Efficacy
KW - Ethics
KW - Human challenge
KW - Infection models
KW - Vaccine
UR - http://www.scopus.com/inward/record.url?scp=85044262274&partnerID=8YFLogxK
U2 - 10.1016/j.biologicals.2018.02.002
DO - 10.1016/j.biologicals.2018.02.002
M3 - Article
C2 - 29573967
AN - SCOPUS:85044262274
SN - 1045-1056
VL - 61
SP - 85
EP - 94
JO - Biologicals
JF - Biologicals
ER -