TrialSignal
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
Aug 04, 2026
Report code
NCT04232280-Aug 04, 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 successful development of this vaccine could address a significant unmet need in CMV prevention, particularly in populations at risk of congenital CMV infection. The market potential is substantial, given the prevalence of CMV and the lack of approved vaccines. Competitive analysis indicates that while several companies are exploring CMV vaccines, Moderna's mRNA platform provides a technological edge, potentially leading to faster development timelines and robust immune responses. Diligence should focus on safety data, immunogenicity results, and the regulatory pathway as the trial progresses towards pivotal Phase 3 studies.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT04232280
Indication
Cytomegalovirus Infection
Modality
RNA therapy
Target
Cytomegalovirus (CMV) antigens, specifically 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.