Ireland
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Recruiting Phase 3

A Phase III Control Study of the Safety and Immunogenicity of vYF in Pediatric Population

NCT07103148 · tracked via the Priya Life Science Mexico tracker
Sponsor
Phase
Phase 3
Started
2025-07-11
Last updated
2026-05-06

Condition(s) studied

Yellow Fever Immunization

Investigational drug(s) / intervention(s)

Yellow fever vaccine (live) →Yellow fever vaccine (live) →Yellow fever vaccine (live) →Measles, combinations with mumps and rubella, live attenuated

Yellow fever vaccine (live): Powder and diluent for suspension for injection Subcutaneous

Yellow fever vaccine (live): Powder and diluent for suspension for injection Subcutaneous

Yellow fever vaccine (live): Powder and diluent for suspension for injection Subcutaneous

Measles, combinations with mumps and rubella, live attenuated: Powder, lyophilized, for suspension for reconstitution Subcutaneous or intermuscular

Study summary

The purpose of this study is to determine whether vYF (investigational vaccine) is safe and can help the body to develop antibodies (immunogenicity) compared with Stamaril vaccine and YF-VAX vaccine (both licensed vaccines) and when they are co-administered with Measles Mumps Rubella (MMR) vaccines in infants aged 11-15 months.

Number of Participants:

A total of 2440 participants is planned to be enrolled in VYF04 study.

Study Arms and Duration:

Eligible participants will be randomized in 2 independent groups (9-24 months, 2-5 years) to receive 1 dose of either vYF or Stamaril or YF-VAX in a 2:1:1 ratio within each age group. An additional group with participants of 11-15 months of age will also receive at the same vaccination visit vYF and a single dose of MMR vaccine.

For the 2nd step (YF booster vaccine administration in a subset), at the Year (Y) 3 visit, a subset of 120 participants of the 9-24 months of age group who did receive a YF vaccine on Day(D) 01 will be invited to join a booster dose assessment (booster dose administered after the Y3 visit blood sample has been taken). Participants aged 11 to 15 months at the time of the concomitant administration of vYF and MMR will not be eligible for receiving a booster dose.

The duration of each participation will be approximately 3 years for all participants (including participants co-administered on D01 with vYF and MMR), and 6 more months post-booster dose administration for the participants enrolled in the booster subset.

Eligibility

Sex
ALL
Min age
9 Months
Max age
5 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Aged 9 months to 5 years on the day of inclusion\* \* "9 months to 5 years" means from the day of the 9th month after birth to the day before the 6th year birthday * Aged 11 to 15 months\* on the day of inclusion for participants enrolled in the MMR co-administration group \* "11 to 15 months" means from the day of the 11th month after birth to the day before the 16th month birthday * Participants who are healthy as determined by medical evaluation including medical history and physical examination * For infants\*, born after a gestation period of 27 through 36 weeks and medically stable as assessed by the investigator, based on the following definition: "Medically stable" refers to the condition of premature infants who do not require significant medical support or ongoing management for debilitating disease and who have demonstrated a clinical course of sustained recovery by the time they receive the first dose of study intervention \* Infants aged 9 months to 11 months up to the day before the 12th month birthday * Participant and parent/LAR are able to attend all scheduled visits and to comply with all study procedures * ICF has been signed and dated by the parent(s) or other LAR (and by an independent witness if required by local regulations) Exclusion Criteria: Participants are excluded from the study if any of the following criteria apply: * Known or suspected congenital or acquired immunodeficiency; or receipt of immunosuppressive therapy, such as anti-cancer chemotherapy irradiation therapy, within the preceding 6 months; or long-term systemic corticosteroid therapy (prednisone or equivalent for more than 2 consecutive weeks within the past 3 months) * Known history of FV infection * Known systemic hypersensitivity to any of the study intervention components, eggs or history of a life-threatening reaction to the study interventions used in the study or to a product containing any of the same substances * Moderate or severe acute illness/infection (according to Investigator judgment) or febrile illness (temperature ≥ 38.0°C \[≥ 100.4°F\]) on the day of study intervention administration. A prospective participant should not be included in the study until the condition has resolved or the febrile event has subsided. * Chronic illness\* that, in the opinion of the Investigator, is at a stage where it might interfere with study conduct or completion , including malignancy, such as leukemia, or lymphoma \*Chronic illness may include, but is not limited to, cardiac disorders, renal disorders, auto-immune disorders, diabetes, psychiatric disorders or chronic infection * History of central nervous system disorder or disease, including seizures and febrile seizures * Receipt of any vaccine in the 4 weeks preceding the study intervention administration or planned receipt of any vaccine in the 4 weeks following the study intervention administration. Vaccine to be administered as part of the National Immunization Schedule will be postponed after the D29 visit * Previous vaccination against a FV disease at any time including YF with an investigational or marketed vaccine * Receipt of immune globulins, blood or blood-derived products in the past 6 months * Administration of any anti-viral within 2 months preceding the study intervention administration and up to the 6 weeks following the study intervention administration * For participants enrolled in the MMR co-administration group: previous vaccination against measles, measles/mumps/rubella * For participants enrolled in the MMR co-administration group: history of measles, mumps, rubella confirmed either clinically, serologically, or microbiologically * Known history or laboratory evidence of HIV infection * Known history of hepatitis B or hepatitis C seropositivity * Personal or family history of thymic pathology (thymoma, thymectomy, or myasthenia) * Participation at the time of study enrollment (or in the 4 weeks preceding the study intervention administration) or planned participation during the first year of the 3-year follow-up in another clinical study investigating a vaccine, drug, medical device, or medical procedure. Enrollment in another study after the first 6 months of follow-up is permitted, assuming it does not exclude participation in this study. * In an emergency setting, or hospitalized involuntary * Identified as a natural or adopted child of the Investigator or employee with direct involvement in the proposed study

Primary outcome measure(s)

  • Percentage of participants with seroconversion to YF virus after 1 dose of vYF compared to seroconversion after 1 dose of the Stamaril in YF-naive participants (9-24 months) — At Day 29, 28 days post-vaccination (on Day 01) with vYF or Stamaril
    Seroconversion rates will be assessed using a YF MN assay Seroconversion is defined as a 4-fold increase in NAb titers as compared to the pre-vaccination value
  • Percentage of participants with seroconversion to YF virus after 1 dose of vYF compared to seroconversion after 1 dose of the YF-VAX in YF-naive participants (9-24 months) — At Day 29, 28 days post-vaccination (on Day 01) with vYF or YF-VAX
    Seroconversion rates will be assessed using a YF MN assay Seroconversion is defined as a 4-fold increase in NAb titers as compared to the pre-vaccination value
  • Percentage of participants with seroconversion to YF virus after 1 dose of vYF compared to seroconversion after 1 dose of the Stamaril in YF-naive participants (2-5 years) — At Day 29, 28 days post-vaccination (on Day 01) with vYF or Stamaril
    Seroconversion rates will be assessed using a YF MN assay Seroconversion is defined as a 4-fold increase in NAb titers as compared to the pre-vaccination value
  • Percentage of participants with seroconversion to YF virus after 1 dose of vYF compared to seroconversion after 1 dose of the YF-VAX in YF-naive participants (2-5 years) — At Day 29, 28 days post-vaccination (on Day 01) with vYF or YF-VAX
    Seroconversion rates will be assessed using a YF MN assay Seroconversion is defined as a 4-fold increase in NAb titers as compared to the pre-vaccination value

Trial sites (13)

FacilityCityRegionStatus
Investigational Site Number : 3400001 San Pedro Sula Honduras Recruiting
Investigational Site Number : 3400005 San Pedro Sula, Cortes Honduras Recruiting
Investigational Site Number : 3400002 Tegucigalpa Honduras Recruiting
Investigational Site Number : 3400003 Tegucigalpa Honduras Recruiting
Investigational Site Number : 3400007 Tegucigalpa Honduras Recruiting
Investigational Site Number : 4840007 Torreón Coahuila Recruiting
Investigational Site Number : 4840013 Cuernavaca Morelos Recruiting
Investigational Site Number : 4840015 Tizimín Yucatán Recruiting
Investigational Site Number : 4840009 Chihuahua City Mexico Recruiting
Investigational Site Number : 4840005 Ecatepec de Morelos Mexico Recruiting
Investigational Site Number : 5910001 Panama City Panama Recruiting
Investigational Site Number : 5910002 Panama City Panama Recruiting
Investigational Site Number : 5910003 Panama City Panama Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07103148 on ClinicalTrials.gov ↗ ← All trials in Mexico