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NCT04232280COMPLETEDanonymous

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

Sponsor

Source record

ModernaTX, Inc.

Phase

Source record

Phase 2

Modality

AI-normalized

RNA therapy

Target

AI-normalized

Cytomegalovirus (CMV) immunogenicity through mRNA technology, targeting the immune response to CMV infections.

Indication / condition

AI-normalized

Cytomegalovirus Infection

Intervention

Source record

mRNA-1647, Placebo

Source & freshness

Source record

NCT ID

NCT04232280

Original source

ClinicalTrials.gov

Source last updated

May 05, 2026

Ingested at

Jun 19, 2026

Internal sync

Jun 19, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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NCT ID

NCT04232280

Title

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

Sponsor

ModernaTX, Inc.

Status

COMPLETED

Phase

Phase 2

Condition raw

Cytomegalovirus Infection

Condition normalized

Cytomegalovirus Infection

Modality raw

RNA therapy

Modality normalized

RNA therapy

Target raw

Cytomegalovirus (CMV) immunogenicity through mRNA technology, targeting the immune response to CMV infections.

Target normalized

Cytomegalovirus (CMV) immunogenicity through mRNA technology, targeting the immune response to CMV infections.

Interventions

mRNA-1647, Placebo

Public preview

Source record

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.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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