← Back to Clinical Trials
Recruiting NCT06577363

NCT06577363 A Survey of Maribavir Tablets in Participants With Cytomegalovirus Infection

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06577363
Status Recruiting
Phase
Sponsor Takeda
Condition Cytomegalovirus (CMV)
Study Type OBSERVATIONAL
Enrollment 250 participants
Start Date 2024-08-28
Primary Completion 2031-08-30

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Maribavir

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 250 participants in total. It began in 2024-08-28 with a primary completion date of 2031-08-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study is a survey in Japan of Maribavir tablets used to treat participants with Cytomegalovirus (CMV) infection refractory to existing anti-CMV therapy in organ transplantation (including hematopoietic stem cell transplantation). The main aim of the study is to check if treatment with Maribavir can protect Japanese people against CMV infection, and to check side effect from the study treatment. The study sponsor will not be involved in how the participants are treated but will provide instructions on how the clinics will record what happens during the study. During the study, participants with CMV infection will take Maribavir tablets according to their clinic's standard practice. The study doctors will check for side effects from Maribavir tablets for 27 weeks.

Eligibility Criteria

Inclusion Criteria: \- All participants with Cytomegalovirus (CMV) infection refractory to existing anti-CMV therapy in organ transplantation (including hematopoietic stem cell transplantation). Exclusion Criteria: \- None

Contact & Investigator

Central Contact

Takeda Contact

✉ medinfoUS@takeda.com

📞 +1-877-825-3327

Principal Investigator

Study Director

STUDY DIRECTOR

Takeda

Frequently Asked Questions

Who can join the NCT06577363 clinical trial?

This trial is open to participants of all sexes, studying Cytomegalovirus (CMV). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06577363 currently recruiting?

Yes, NCT06577363 is actively recruiting participants. Contact the research team at medinfoUS@takeda.com for enrollment information.

Where is the NCT06577363 trial being conducted?

This trial is being conducted at Tokyo, Japan.

Who is sponsoring the NCT06577363 clinical trial?

NCT06577363 is sponsored by Takeda. The principal investigator is Study Director at Takeda. The trial plans to enroll 250 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology