Safety and Immunogenicity of a Single Dose of the Recombinant Live-Attenuated Respiratory Syncytial Virus (RSV) Vaccines RSV ΔNS2/Δ1313/I1314L, RSV 6120/ΔNS2/1030s, RSV 276 or Placebo, Delivered as Nose Drops to RSV-Seronegative Children 6 to 24 Months of Age

Stopped early · Phase 1/Phase 2 · Has a placebo group

Conditions studied: Respiratory Syncytial Virus (RSV)

In brief

The purpose of this study was to evaluate the safety and immunogenicity of a single dose of the recombinant live-attenuated respiratory syncytial virus (RSV) vaccines, RSV ΔNS2/Δ1313/I1314L, RSV 6120/ΔNS2/1030s, and RSV 276, in RSV-seronegative children 6 to 24 months of age.

Key facts

Study ID: NCT03916185
Run by: National Institute of Allergy and Infectious Diseases (NIAID)
People needed: 67
Starts: 2019-06-20
Expected to finish: 2024-04-25
Last updated by the study team: 2025-02-21

Who can join

Age: 1 and older, up to 2. Sex: any. Healthy volunteers: accepted.

You may qualify if…

In good health based on review of the medical record, history, and physical examination, without evidence of chronic disease.
Parent/guardian is willing and able to provide written informed consent as described in the study protocol.
Seronegative for RSV antibody, defined as a serum RSV-neutralizing antibody titer less than 1:40 at screening from a sample collected no more than 42 days prior to study product administration.
Note: results from specimens collected during screening for any study of an RSV vaccine developed by the Laboratory of Infectious Diseases (LID) (National Institute of Allergy and Infectious Diseases [NIAID], National Institutes of Health [NIH]) are acceptable. If study product will not be administered the same day as randomization (see the study protocol), it must be administered no more than 42 days after the screening sample is collected.
Growing normally for age in the opinion of the site clinician in the six months prior to enrollment AND has a current height and weight above the 3rd percentile for age and sex per Centers for Disease Control and Prevention (CDC) World Health Organization (WHO) growth standards.
Has received routine immunizations appropriate for age (as per national Center for Disease Control Advisory Committee on Immunization Practices [ACIP]). Note: COVID-19 vaccination will not be required unless fully licensed for this age group and ACIP-recommended. See study-specific Manual of Procedures for further guidance
Is expected to be available for the duration of the study.
If born to an HIV-infected woman, potential participant must have documentation of 2 negative HIV nucleic acid (RNA or DNA) test results from samples collected on different dates with both collected when greater than or equal to 4 weeks of age and at least one collected when greater than or equal to 16 weeks of age, and no positive HIV nucleic acid (RNA or DNA) test; or 2 negative HIV antibody tests, both from samples collected at greater than or equal to 24 weeks of age. If potential participant was breastfed by an HIV-infected woman, each of the sampling times noted above must be measured in weeks after the last exposure to breast milk, rather than weeks of age.

You may not qualify if…

Prior laboratory-confirmed RSV infection.
Known or suspected HIV infection or impairment of immunological functions.
Receipt of immunosuppressive therapy, including any systemic, nasal, or inhaled corticosteroids within 28 days of enrollment. Note: Cutaneous (topical) steroid treatment is not an exclusion.
Any receipt of bone marrow/solid organ transplant.
Major congenital malformations (such as congenital cleft palate) or cytogenetic abnormalities.
Previous enrollment in this trial, previous pediatric receipt of a licensed or investigational RSV vaccine, or previous maternal or pediatric receipt of or planned administration of any other anti-RSV product (such as ribavirin or RSV IG or RSV monoclonal antibody [mAb]) within 4 months of screening or planned administration of an anti-RSV product between screening and day 56 after enrollment.
Any previous anaphylactic reaction.
Any known hypersensitivity to any study product component.
Heart disease. Note: Potential participants with cardiac abnormalities documented to be clinically insignificant and requiring no treatment may be enrolled.
Lung disease, including any history of reactive airway disease or medically diagnosed wheezing.
Member of a household that contains a person with chronic lung disease, including but not limited to chronic obstructive pulmonary disease (COPD), emphysema, or home oxygen use, reactive airway disease or asthma. Note: Asthma or reactive airway disease in a household member is not exclusionary unless the household member has taken oral steroids for asthma management in the past month and/or has been hospitalized for asthma in the past month.
Member of a household that contains, or will contain, an infant who is less than 4 months of age at the enrollment date through Day 14.
Member of a household that contains another child/other children who is/are enrolled or is/are scheduled to be enrolled in IMPAACT 2021 on a different date and has/have not completed the Day 56 visit in the same calendar year (i.e., all eligible children from the same household must be enrolled/receive study product on the same date or additional children in the household may be screened, enrolled, and randomized independently after other children in the household complete the Day 56 Visit).
Member of a household that contains another child who is, or is scheduled to be, enrolled in another study evaluating an intranasal live-attenuated RSV vaccine, AND there has been or will be an overlap in residency during Day 0 to 14 of that other child's participation in the study.
Member of a household that contains an immunocompromised individual, including, but not limited to:
a person who has been diagnosed with cancer and who has received chemotherapy within the 12 months prior to enrollment; or
a person living with a solid organ, cord blood, or bone marrow transplant.
Shares a daycare room with infants less than 4 months of age, and parent/guardian is unable or unwilling to suspend daycare for 14 days following study product administration.
Any of the following events at the time of enrollment:
fever (rectal temperature of greater than or equal to 100.4°F (38°C)), or
upper respiratory signs or symptoms (including but not limited to rhinorrhea, cough, or pharyngitis) or
nasal congestion significant enough to interfere with successful study product administration, or
otitis media.
Note: if participant is randomized and subsequently noted to have any of the above, study product administration must be deferred per the study protocol.
Receipt of the following prior to enrollment (start counting backwards with '1' as the day of planned study product administration):

Where it is running

David Geffen School of Medicine at UCLA NICHD CRS — Los Angeles, California, United States
University of California, UC San Diego CRS- Mother-Child-Adolescent HIV Program — San Diego, California, United States
Univ. of Colorado Denver NICHD CRS — Aurora, Colorado, United States
Emory University School of Medicine NICHD CRS — Atlanta, Georgia, United States
Rush Univ. Cook County Hosp. Chicago NICHD CRS — Chicago, Illinois, United States
Lurie Children's Hospital of Chicago (LCH) CRS — Chicago, Illinois, United States
University of Maryland School of Medicine Center for Vaccine Development CRS — Baltimore, Maryland, United States
The Children's Mercy Hospital CRS — Kansas City, Missouri, United States
Center for Vaccine Development CRS — St Louis, Missouri, United States
SUNY Stony Brook NICHD CRS — Stony Brook, New York, United States
Jacobi Med. Ctr. Bronx NICHD CRS — The Bronx, New York, United States
Duke Vaccine and Trials Unit CRS — Durham, North Carolina, United States
Gamble Center for Clinical Studies CRS — Cincinnati, Ohio, United States
Baylor College of Medicine/ Texas Children's Hospital NICHD CRS — Houston, Texas, United States

Full record on ClinicalTrials.gov

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