Prospective Surveillance of Respiratory Syncytial Virus Disease in Infants and Toddlers

Sanofi

Status: Completed

Conditions: Respiratory Syncytial Virus Infections

Study type: Observational

Funder types: Industry

Identifiers

NCT05964582

VAD00019

U1111-1281-0204 (Registry Identifier)

Details and patient eligibility

About

The study is a multi-center, multi-national, prospective surveillance study in which the study participants will not receive a study vaccine but will provide a baseline blood sample and be followed for acute respiratory disease during 6 months. The 6-month follow-up will occur for the most part during the Respiratory Syncytial Virus(RSV) season (based on enrollment timing and as per feasibility). A maximum of 1000 children from 6 to < 22 months of age are planned to be enrolled in 5 to 10 countries, 1 to 2 sites per country, targeting approximately 100 participants per country. The purpose of the study is to assess the seroprevalence and incidence of RSV disease during the study period in the targeted countries and sites for a Phase III vaccine study.

Full description

The duration of the study will be 6 months for each participant.

Enrollment: 344 patients

Sex: All

Ages: 6 to 21 months old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Aged 6 months to < 22 months on the day of inclusion (means the day of the 6-month birthday to the day before the 22-month birthday)
• Participants who are healthy as determined by medical evaluation including medical history
• Born at full term of pregnancy (≥ 37 weeks) or 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 are enrolled in the study

Exclusion criteria

• Known or suspected congenital or acquired immunodeficiency; or receipt of immunosuppressive therapy, such as anti-cancer chemotherapy or radiation 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)

• Chronic illness that, in the opinion of the investigator, is at a stage where it might interfere with study conduct or completion

• Probable or confirmed ongoing case of viral respiratory infection (including COVID-19, influenza, rhinovirus, etc.) at the time of enrollment. A prospective participant should not be included in the study until the respiratory infection has resolved

• Member of a household that contains an immunocompromised individual, including, but not limited to:

  • a person who is human immunodeficiency virus (HIV) infected
  • a person who has received chemotherapy within the 12 months prior to study enrollment
  • a person who has received (within the past 6 months) or is receiving (at the time of enrollment) immunosuppressant agents
  • a person living with a solid organ or bone marrow transplant

• Participant's mother previous receipt or planned administration of an investigational RSV vaccine during pregnancy and/or breastfeeding

• Receipt or planned receipt of any of the following vaccines:

  • Any intranasal live attenuated vaccine within the 28 days prior to enrollment
  • Any injectable live attenuated vaccine within the 28 days prior to and after enrollment

• Previous receipt of an investigational RSV vaccine or receiving any anti-RSV product (such as ribavirin or RSV immune globulin or RSV monoclonal antibody) less than 6 months before enrollment

• Receipt of immune globulins, blood or blood-derived products in the past 3 months

• Participation at the time of study enrollment or planned participation during the present study period in another clinical study investigating a vaccine, drug, medical device, or medical procedure

The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial

Trial design

344 participants in 1 patient group

Healthy children aged 6 months to < 22 months

Description:

No vaccine will be administered. All enrolled participants will have a blood sample collected at enrollment (visit 01) and a nasal swab collected each time they have an RSV-like illness visit