Moreover, CVD-Mali and the Ministry of Health propose to

quantify the impact of RV vaccine introduction on the burden of RV disease. This research study was funded by PATH’s Rotavirus Vaccine Program under a grant from the GAVI Alliance, and was co-sponsored by Merck & Co., Inc. The study was designed by scientists from Merck & Co., Inc, with substantial input from PATH staff and site investigators. PATH staff independently monitored study execution in Mali and participated in pharmacovigilance and data analyses. We also acknowledge the sincere effort of all our study staffs in Mali at CVD-Mali, Centre National d’Appui à la lute contre la Maladie (CNAM), the Ministry of Health of Mali, the Direction de la Pharmacie et du Medicament (DPM), The CHU-Hopital Gabriel Touré (CHU-HGT),

CSCOMs Akt inhibitor ASACODA, ADASCO, ASACONIA, ANIASCO; traditional healers, religious and socio-cultural leaders; and the support of the community members throughout the study area without which this study would ever have been materialized. Special thank to study personnel at Center for Vaccine Developpment (CVD), University SAR405838 clinical trial of Maryland: Karen S Ball, and to personnel at CVD-Mali: Kindia Camara. Conflict of interest statement: SOS received Merck funding as a member of the Advisory Board for Pediatric Vaccines and Vaccine New Products; MC was an employee of Merck when the clinical trial was conducted and owned equity in the company. MML is a paid advisory board member for NIH Vaccine Center, Center for Clinical Vaccinology and Tropical Medicine at Oxford University, AlphaVax, International Vaccine Institute, Centre de Recerca en Salut Internacional de Barcelona, AfriChol, and the Pasteur Institute STOPENTERICS program, and has received consultancies from Novartis

and Merck. No other conflicts of interest are declared. “
“Annually, rotavirus gastroenteritis (RVGE) kills more than Ketanserin 453,000 children around the world [1] and [2]. The highest mortality rates are experienced by children less than 1 year of age in developing countries, particularly in Africa and Asia. Since 2006, children born in the United States and many countries in Latin America and Europe have benefited from life-saving rotavirus vaccines but, without demonstrated efficacy in Africa and Asia, the WHO Strategic Advisory Group of Experts (SAGE) on Immunization recommended that clinical trials be conducted in these areas of the world [3] to demonstrate their immunogenicity and efficacy. Over the last several years, these studies have been performed with both Rotarix® and Rotateq®, the two rotavirus vaccines that are currently on the market [4], [5] and [6].