mRNA Vaccine for Cytomegalovirus (CMV)

Enrolling by invitation at 5 trial locations
Age: 18 - 65
Sex: Any
Trial Phase: Phase 2
Sponsor: ModernaTX, Inc.
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests an mRNA vaccine designed to protect against cytomegalovirus (CMV), a virus many people carry unknowingly. The goal is to determine how long the immune response lasts and whether a booster shot enhances it. Participants from the earlier phase of the study who received the vaccine (not a placebo) can join. It suits those who are either CMV-positive or CMV-negative and have previously participated in the initial study. As a Phase 2 trial, this research measures the treatment's effectiveness in a smaller group, allowing participants to contribute to important findings.

Do I need to stop my current medications for this trial?

The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial team or your doctor.

Is there any evidence suggesting that the mRNA-1647 vaccine is likely to be safe for humans?

Previous studies have shown that mRNA-1647 is generally safe and well-tolerated. Research demonstrated that at all dose levels, it triggered immune responses specific to the substances causing an immune reaction. An independent data safety monitoring board reviewed the vaccine, conducting a thorough safety check and finding no major issues. Overall, the evidence suggests that mRNA-1647 is safe for use in humans.12345

Why do researchers think this study treatment might be promising?

Researchers are excited about the mRNA-1647 vaccine for cytomegalovirus (CMV) because it uses cutting-edge mRNA technology to train the immune system to recognize and combat the virus. Unlike traditional treatments that often involve antiviral medications, mRNA-1647 aims to prevent CMV infection by prompting the body to produce proteins that trigger an immune response against the virus. This approach is innovative because it not only targets the virus directly but also offers a preventative strategy, potentially reducing the risk of CMV-related complications in vulnerable populations.

What evidence suggests that the mRNA-1647 vaccine could be effective for cytomegalovirus?

Research has shown that the mRNA-1647 vaccine can help the body combat CMV, a virus affecting adults. Early studies found the vaccine to be generally safe. These studies also demonstrated that the vaccine could prevent CMV infection in 6% to 23% of cases, depending on the measurement of effectiveness. While these results are promising, further research is needed to fully understand the vaccine's efficacy. In this trial, participants may receive a booster dose of the mRNA-1647 vaccine to evaluate the duration of its protection and its safety, particularly with the booster dose.13678

Are You a Good Fit for This Trial?

This trial is for adults who participated in a prior CMV vaccine study (mRNA-1647-P202) and received the mRNA-1647 vaccine, not placebo. They must have completed that study, be in good health as judged by the investigator, understand and agree to follow trial procedures, and provide written consent. Those previously vaccinated with any CMV vaccine other than mRNA-1647 or with conditions affecting safety assessments or adherence to procedures cannot join.

Inclusion Criteria

Understands and agrees to comply with the trial procedures and provides written informed consent.
According to the assessment of the Investigator, is in good general health and is capable of complying with trial procedures.
I was CMV negative at my initial and final study visits.
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Exclusion Criteria

Diagnosis or condition that, in the judgment of the Investigator, may affect participant safety, assessment of safety endpoints, assessment of immune response, or adherence to trial procedures, including any medical, psychiatric, or occupational condition that, in the opinion of the Investigator, might pose additional risk due to participation in the study or could interfere with the interpretation of study results.
I have not received any CMV vaccine except for mRNA-1647.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Primary Extension Phase

Participants who completed Study mRNA-1647-P202 will be followed every 6 months for 3 years to evaluate long-term immune persistence and safety.

3 years
Every 6 months

Optional Booster Phase

Participants may opt to receive a single booster dose of the mRNA-1647 vaccine or be followed without receiving the booster.

12 months
Followed until BP Month 12

Follow-up

Participants are monitored for safety and effectiveness after the optional booster phase.

6 months

What Are the Treatments Tested in This Trial?

Interventions

  • mRNA-1647
Trial Overview The focus of this extension study is on evaluating how long the immune response lasts from the mRNA-1647 vaccine given to both CMV-seronegative and CMV-seropositive adults. It's a continuation for participants who were part of an earlier phase where they received this experimental vaccine against Cytomegalovirus.
How Is the Trial Designed?
3Treatment groups
Experimental Treatment
Group I: Primary Extension PhaseExperimental Treatment1 Intervention
Group II: Optional Booster Phase - Observational GroupExperimental Treatment1 Intervention
Group III: Optional Booster Phase - BD RecipientsExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

ModernaTX, Inc.

Lead Sponsor

Trials
127
Recruited
66,790,000+

Dr. Stephen Hoge

ModernaTX, Inc.

Chief Medical Officer

MD from Harvard Medical School

Stéphane Bancel profile image

Stéphane Bancel

ModernaTX, Inc.

Chief Executive Officer since 2011

MBA from Harvard Business School, MSc in Engineering from École Centrale Paris

Published Research Related to This Trial

Congenital cytomegalovirus (CMV) infection is the leading infectious cause of disability in newborns, highlighting the urgent need for effective vaccination to protect vulnerable populations.
Current research shows promise for a recombinant CMV glycoprotein B (gB) vaccine, which has demonstrated some efficacy in preventing CMV infection in young women, adolescents, and CMV-seronegative transplant recipients, indicating potential for broader immunization strategies.
Cytomegalovirus vaccines under clinical development.Schleiss, MR.[2022]
Certain high-risk groups, such as HIV-infected individuals, transplant patients, and newborns, are particularly vulnerable to diseases caused by human cytomegalovirus (CMV), highlighting the need for effective vaccination strategies.
While there are currently no licensed CMV vaccines for humans, various vaccine approaches, including protein subunit, DNA, and live attenuated vaccines, are being tested in clinical trials, showing promise in inducing protective immune responses against CMV.
Progress toward an elusive goal: current status of cytomegalovirus vaccines.Schleiss, MR., Heineman, TC.[2007]
A recent trial of a subunit glycoprotein B (gB) vaccine with the adjuvant MF59 showed promise in reducing CMV infections in postpartum women, indicating potential for effective CMV vaccination.
Various innovative vaccine strategies, including replicons and DNA vaccines, are currently in clinical trials, but the ideal formulation for a CMV vaccine is still being determined.
Vaccines for cytomegalovirus.Bernstein, DI.[2019]

Citations

Reflecting on Moderna's Phase 3 CMV Vaccine ReadoutToday, we announced topline results from a Phase 3 pivotal trial evaluating the efficacy of mRNA-1647, our investigational cytomegalovirus (CMV ...
Overview of mRNA-1647: Investigational CMV Vaccine• 43-50% efficacy for CMV infection in 2 previous trials of recombinant gB candidate vaccine1 ... mRNA-1647 Phase 3 Efficacy Trial: Two Planned ...
Moderna's CMV Vaccine Candidate Misses in Late Stage ...Vaccine efficacy against CMV infection was reported to be between 6% to 23% depending on the case definition used. Based on these findings, the ...
Results From a Phase 1 Randomized Clinical Trial - PMCThis phase 1, first-in-human trial demonstrated that mRNA-1647 has an acceptable safety profile in adults and elicits humoral and cellular immune responses.
NCT05085366 | A Study to Evaluate the Efficacy, Safety ...The main purpose of this study is to evaluate the efficacy of mRNA 1647 vaccine in CMV-seronegative female participants and to evaluate the safety and ...
2892. Safety and Immunogenicity of mRNA-1647, an ...Conclusion. mRNA-1647 was generally safe and well-tolerated and induced antigen-specific immune responses at all dose levels in both CMV- ...
A Clinical Trial of a Cytomegalovirus (CMV) Vaccine ...The purpose of this clinical trial is to evaluate the safety and efficacy of mRNA-1647 investigational vaccine against CMV and evaluate the safety of the mRNA- ...
Results From a Phase 1 Randomized Clinical Trial | The ...This phase 1, first-in-human trial demonstrated that mRNA-1647 has an acceptable safety profile in adults and elicits humoral and cellular immune responses.
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