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NCT07020533 · ClinicalTrials.gov registry record · Phase 1

A Vaccine (CMV-MVA Triplex Vaccine) for the Enhancement of CMV-Specific Immunity and the Prevention of CMV Viremia in Patients Undergoing Haploidentical Hematopoietic Stem Cell Transplant

A Phase 1 study, sponsored by City of Hope Medical Center.

Recruiting
Registry status
Phase 1
Development phase
46
Enrollment target

NCT07020533: Recruiting Phase 1 study, sponsored by City of Hope Medical Center.

NCT07020533 is a Phase 1 study that is actively recruiting participants, run by City of Hope Medical Center. The registered enrollment target is 46 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (23% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07020533, a Phase 1 study, is actively recruiting participants, sponsored by City of Hope Medical Center.

RECRUITING
Registry status
Phase 1
Development phase
46 participants
Enrollment target

Study Summary

This phase Ib trial tests the safety, side effects, and how well cytomegalovirus (CMV)-modified vaccinia Ankara (MVA) Triplex vaccine works in enhancing CMV-specific immunity and preventing CMV viremia in patients undergoing haploidentical hematopoietic stem cell transplant. Haploidentical stem cell transplantation (haploHCT) has advanced to become the predominant procedure for patients lacking a matched donor. Compared to matched related donor transplants, the rate of significant CMV infection is higher in patients undergoing a haploHCT. Significant CMV infection is associated with an increased risk of complications and death. Vaccination is the main preventative approach to limit complications and death in immunocompromised patients at high risk of post-stem cell transplant infections. CMV-MVA Triplex vaccine, is a CMV vaccine based on the attenuated poxvirus, modified vaccinia Ankara (MVA), developed to enhance CMV-specific immunity in both healthy stem cell transplant donors and stem cell transplant patients to prevent significant CMV infection post-stem cell transplant. Giving CMV-MVA triplex vaccine may be safe, tolerable and/or effective in enhancing cytomegalovirus (CMV)-specific immunity and preventing CMV viremia in patients undergoing a haploHCT.

Primary Outcome

Will evaluate for CMV reactivation prompting antiviral therapy. Will be evaluated in patients that received a stem cell infusion from a Triplex vaccinated haploidentical donor and received the first Triplex vaccination.

Interventions

  • PROCEDURE Biospecimen Collection
  • OTHER Electronic Health Record Review
  • DRUG Letermovir
  • BIOLOGICAL Multi-peptide CMV-Modified Vaccinia Ankara Vaccine
  • PROCEDURE Haploidentical Hematopoietic Cell Transplantation

Trial Details

FieldValue
Enrollment Target 46 participants
Start Date 2026-05-08
Est. Completion 2029-05-30
Phase Phase 1
City of Hope Medical Center

582 total trials

What NCT07020533 shows while recruiting

NCT07020533 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 46 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (23% lower).

The record links to 0 conditions, and to 5 interventions - of which Biospecimen Collection is the first listed.

NCT07020533 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07020533 about?

NCT07020533 is a clinical study titled "A Vaccine (CMV-MVA Triplex Vaccine) for the Enhancement of CMV-Specific Immunity and the Prevention of CMV Viremia in Patients Undergoing Haploidentical Hematopoietic Stem Cell Transplant". This phase Ib trial tests the safety, side effects, and how well cytomegalovirus (CMV)-modified vaccinia Ankara (MVA) Triplex vaccine works in enhancing CMV-specific immunity and preventing CMV viremia in patients undergoing haploidentical hematopoietic stem cell transplant. Haploidentical stem cell...

What is the current status of trial NCT07020533?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 46 participants. The study started on 2026-05-08. Estimated completion is 2029-05-30.

What interventions are being tested in trial NCT07020533?

The interventions under investigation include: Biospecimen Collection (PROCEDURE), Electronic Health Record Review (OTHER), Letermovir (DRUG), Multi-peptide CMV-Modified Vaccinia Ankara Vaccine (BIOLOGICAL), Haploidentical Hematopoietic Cell Transplantation (PROCEDURE).

Who is sponsoring clinical trial NCT07020533?

This trial is sponsored by City of Hope Medical Center, which has 582 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07020533's enrollment target sits among peer trials

46 1058th of 2000 higher than 935 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07020533, the US trial registry maintained by the National Library of Medicine. NCT07020533 (small enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.