Moderna Inc. announced topline results from a Phase 3 pivotal trial evaluating its investigational cytomegalovirus (CMV) vaccine, mRNA-1647. The study did not meet its primary efficacy endpoint of preventing CMV infection in seronegative female participants of childbearing age. As a result, Moderna will discontinue its congenital CMV clinical development program. The company indicated that the majority of the data from this trial is still forthcoming and will be shared with the scientific community in the future. Moderna will continue evaluating mRNA-1647 in an ongoing Phase 2 trial in bone marrow transplant patients. The company stated that these developments do not impact its 2025 financial guidance or its expectation of achieving breakeven in 2028.