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Clinical trial intelligence report
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 20, 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 seropositive healthy adults aged 18-40. The successful development of this vaccine could address a significant unmet need in CMV prevention, particularly in congenital infections. The market potential is substantial, given the prevalence of CMV and the lack of approved vaccines. Competitive landscape includes other vaccine candidates in development, but Moderna's established mRNA technology platform provides a competitive edge. Diligence should focus on safety data and immunogenicity results, as these will be critical for advancing to Phase 3 trials and eventual commercialization.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT04232280
Indication
Cytomegalovirus Infection
Modality
RNA therapy
Target
Cytomegalovirus (CMV) vaccine targeting immune response through mRNA technology.
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.