V160-001-002: A Phase I Randomized, Double-Blind, Placebo-Controlled, Dose-Escalation Study to Evaluate the Safety, Tolerability and Immunogenicity of the Human Cytomegalovirus Vaccine (V160) in Healthy Adults

Project: Research project

Project Details

StatusFinished
Effective start/end date6/27/146/26/18

Funding

  • Merck Sharp and Cohme Corporation: $269,872.00