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Follow-up research of JVC-001 Phase III Study (Specific Clinical Research)

Follow-up study of mumps, measles and rubella infection and persistence of immunity in JVC-001 Phase III study subjects (Specific Clinical Research)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCTs031230590
Enrollment
861
Registered
2024-01-24
Start date
2024-02-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Not applicable Not applicable

Interventions

Not applicable

Sponsors

Shindo Shizuo
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Participation in the study participants who have obtained the voluntary written consent from the father, mother, grandfather, or grandmother of the study subjects and who satisfy the following inclusion criteria and do not violate the exclusion criteria are eligible. Inclusion criteria 1) those who have been enrolled in the J301 trial and received the clinical trial vaccine 2) those who have been judged by the principal investigator or co-investigator to have no problems participating in this study

Exclusion criteria

Exclusion criteria: 1) those who have received an additional dose of combined measles-rubella vaccine (MR vaccine) or mumps vaccine

Design outcomes

Primary

MeasureTime frame
1) The incidence of measles, rubella, and mumps from the time of the clinical trial vaccination until the start of this study 2) Antibody titers against measles virus, rubella virus, and mumps virus at the start of this study

Contacts

Public ContactShizuo Shindo

shindo children's clinic

szshindo@nifty.com+81-92-865-7100

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026