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A Phase 2, Randomized, Observer-Blind, Placebo-Controlled, Dose-Finding Trial to Evaluate the Safety and Immunogenicity of Cytomegalovirus Vaccine mRNA-1647 in Healthy Adults
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 19, 2026
NCT ID
NCT04232280
Status
COMPLETED
Phase
Phase 2
Sponsor
ModernaTX, Inc.
Executive brief
Investment-Ready Snapshot
ModernaTX, Inc. is advancing its mRNA-1647 cytomegalovirus vaccine through a Phase 2 clinical trial, focusing on both CMV-seronegative and CMV-seropositive healthy adults aged 18-40. The vaccine's potential to prevent CMV infections, particularly in vulnerable populations such as pregnant women, positions it strategically within the growing vaccine market. Given the increasing prevalence of CMV and the lack of approved vaccines, successful outcomes could lead to significant market opportunities. Competitive analysis indicates that while several companies are exploring CMV vaccines, Moderna's mRNA platform offers a unique technological advantage. Diligence should focus on the trial's safety and immunogenicity data, as well as the regulatory landscape for CMV vaccines.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT04232280
Indication
Cytomegalovirus Infection
Modality
RNA therapy
Target
Cytomegalovirus (CMV) immunogenicity through mRNA technology, targeting the immune response to CMV infections.
Intervention
mRNA-1647, Placebo
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.