Recruiting
Phase 1

Intranasal Vaccine

Sponsor:

Meissa Vaccines, Inc.

Code:

NCT04909021

Conditions

Respiratory Syncytial Virus (RSV)

Eligibility Criteria

Sex: All

Age: 0 - 3

Healthy Volunteers: Accepted

Interventions

Investigational RSV vaccine MV-012-968 (Dosage 1)

Investigational RSV vaccine MV-012-968 (Dosage 2)

Investigational RSV vaccine MV-012-968 (Dosage 3; single-dose)

Investigational RSV vaccine MV-012-968 (Dosage 3; two-dose)

Placebo (single-dose)

Study Details

Brief summary:

This study evaluates an investigational vaccine that is designed to protect humans against infection with respiratory syncytial virus (RSV) and is administered as a nasal spray. Specifically, the study analyzes the safety of, and the immune response to, the vaccine when administered to healthy children between the ages of 6 and 24 months who are seronegative to RSV.

Conditions

Respiratory Syncytial Virus (RSV)

Study ID

NCT04909021

Start date

Jun 3, 2021

Status verified date

Aug, 2022

Completion date

Oct, 2023

Anticipated

Primary completion date

Oct, 2023

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 0 - 3

Healthy Volunteers: Accepted

Key Inclusion Criteria:

1. Children aged 6-36 months
2. Good health based on history, physical examination, and medical record review, without evidence or suspicion of chronic disease
3. Seronegative to RSV, as defined by serum nAb titer below the threshold described in the study protocol and operations manual
4. Written informed consent provided by parent(s)/guardian(s)

Key Exclusion Criteria:

1. Known or suspected chronic illness, particularly cardiopulmonary (including asthma or reactive airways disease), genetic or metabolic, hepatic, renal, infectious (including recurrent or chronic sinusitis), or immunodeficiency
2. Prior lab-confirmed RSV infection
3. Household or close contact (including but not limited to daycare) during the 21 days post-inoculation with anyone < 6 months old or immunocompromised (applies to first study inoculation)
4. Nasal obstruction (including due to anatomic/structural causes, acute or chronic rhinosinusitis, or other causes)
5. Receipt of immunoglobulins, monoclonal antibodies and/or any blood products, or ribavirin within 6 months prior to study inoculation, or planned use during study period
6. Receipt of an investigational RSV vaccine at any time
7. Any other condition that, in the judgment of the investigator, would be a risk to subject's safety and/or may interfere with study procedures or interpretation of results

Study Design

Enrollment

63 participants

Anticipated

Allocation

Randomized

Intervention Model

Sequential

Primary purpose

Prevention

Interventions and Outcome Measures

Arms

experimental: Dosage Group 1: RSV Vaccine Dosage 1

Participants in this arm will receive a single intranasal dose of the investigational RSV vaccine at Dosage 1

experimental: Dosage Group 2: RSV Vaccine Dosage 2

Participants in this arm will receive a single intranasal dose of the investigational RSV vaccine at Dosage 2

experimental: Dosage Group 3: RSV Vaccine Dosage 3 (Single-dose)

Participants in this arm will receive a single intranasal dose of the investigational RSV vaccine at Dosage 3

experimental: Dosage Group 3a: RSV Vaccine Dosage 3 (Two-dose)

Participants in this arm will receive a single intranasal dose of the investigational RSV vaccine at Dosage 3 followed by a second identical dose of the investigational RSV vaccine 28 days later

placebo comparator: Placebo (Single-dose)

Participants in this arm will receive a single intranasal dose of placebo

placebo comparator: Placebo (Two-dose)

Participants in this arm will receive a single intranasal dose of placebo followed by a second identical dose of placebo 28 days later

Interventions

Investigational RSV vaccine MV-012-968 (Dosage 1)

Single dose administered intranasally on Day 1

Investigational RSV vaccine MV-012-968 (Dosage 2)

Single dose administered intranasally on Day 1

Investigational RSV vaccine MV-012-968 (Dosage 3; single-dose)

Single dose administered intranasally on Day 1

Investigational RSV vaccine MV-012-968 (Dosage 3; two-dose)

Single dose administered intranasally on Day 1, followed by an identical dose administered intranasally at the Day 29 study visit

Placebo (single-dose)

Single dose administered intranasally on Day 1

Placebo (two-dose)

Single dose administered intranasally on Day 1, followed by an identical dose administered intranasally at the Day 29 study visit

Primary outcome measure

  • Solicited adverse events (AEs) [ Time Frame: Immediate post-vaccination period ]
  • Unsolicited AEs [ Time Frame: Immediate post-vaccination period ]
  • Serious adverse events (SAEs) [ Time Frame: Full study duration, an average of 1 year ]
  • Medically attended adverse events (MAEs) [ Time Frame: Full study duration, an average of 1 year ]
  • Change in RSV-specific serum neutralizing antibody (nAb) titers (GMT) [ Time Frame: Baseline through Day 28, an average of six (6) weeks ]

Central Contacts and Locations

Central contacts

Locations

MedPharmics

Recruiting

Phoenix, Arizona, United States, 85015

Contacts

Principal Investigator:

Charles S Plimpton, MD

The Emory Children's Center

Recruiting

Atlanta, Georgia, United States, 30322

Contacts

Principal Investigator:

Evan J Anderson, MD

MedPharmics

Recruiting

Metairie, Louisiana, United States, 70006

Contacts

Principal Investigator:

Robert J Jeanfreau, MD

Meridian Clinical Research

Recruiting

Omaha, Nebraska, United States, 68134

Contacts

Principal Investigator:

Brandon Essink, MD

Meridian Clinical Research

Recruiting

Binghamton, New York, United States, 41348

Contacts

Principal Investigator:

Frank Eder, MD

Benchmark Research

Recruiting

San Antonio, Texas, United States, 78240

Contacts

Principal Investigator:

Olutola Adetona, MD

More Information

Sponsor

Meissa Vaccines, Inc.

Last update posted

Aug 2, 2022

Last verified

Aug, 2022

Keywords

  • live attenuated vaccine
  • safety
  • immunogenicity
  • Phase 1 clinical trial
  • Pediatric
  • seronegative
  • children

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-21. This information was provided to ClinicalTrials.gov by Meissa Vaccines, Inc. on 2022-08-02.