Vanderbilt University Medical to Recruit Up to 1,000 COVID-19 Vaccine Trial Volunteers

In late July, Vanderbilt University Medical Center (VUMC) will begin recruiting up to 1,000 volunteers in a late-stage study of an experimental COVID-19 vaccine developed by Moderna Inc. in collaboration with the Vaccine Research Center of the National Institute of Allergy and Infectious Diseases (NIAID) of the National Institutes of Health.

The randomized, placebo-controlled Phase 3 trial will be open to people 18 years old and older. They will receive two shots of either the vaccine or an inactive placebo and will be followed for two years.

The goals of the study are to determine how effective the vaccine is in protecting against COVID-19 and how long the protection lasts. For more information, contact [email protected] or [email protected]

“Vaccine development around COVID-19 is moving at an unprecedented pace due to the remarkable partnerships between academic institutions, the NIH and pharmaceutical industry leaders,” said Buddy Creech, MD, MPH, principal investigator of the NIH-funded Vanderbilt Vaccine and Treatment Evaluation Unit (VTEU).

“We are pressing full speed ahead to provide an answer to this pandemic, while also taking the necessary steps to ensure that new vaccines and therapeutic drugs are both safe and effective,” said Creech, also associate professor of Pediatric Infectious Diseases and director of the Vanderbilt Vaccine Research Program.

VUMC is one of several U.S. centers participating in the nationwide Phase 3 trial, which will enroll 30,000 volunteers over the next two months, officials said.

VTEU and HVTN sites are part of the NIAID-supported COVID-19 Prevention Network (CoVPN), which will harness the resources and expertise of national research networks to rapidly evaluate COVID-19 prevention strategies.

VUMC researchers provided laboratory support of a Phase 1 trial of the vaccine in 45 healthy adults. According to a report published Tuesday in The New England Journal of Medicine, the vaccine had no safety concerns and induced anti-SARS-CoV-2 immune responses in all participants.