Safety of and Immune Response to Recombinant Live Attenuated Parainfluenza Type 3 Virus Vaccine in Healthy Infants and Children

National Institute of Allergy and Infectious Diseases (NIAID)12 enrolled

Overview

Human parainfluenza viruses (HPIVs) are a major health concern in infants and young children under 5 years of age, causing serious respiratory tract disease. The primary purpose of this study is to test the safety of and immune response to a new HPIV vaccine in healthy infants and children.

HPIV type 3 (HPIV3) ranks second only to respiratory syncytial virus as the most important cause of bronchiolitis and pneumonia in infants less than 6 months of age. HPIV3 can cause severe disease in the first 2 years of life and is responsible for 11% of hospitalizations for respiratory diseases in children. This study will evaluate the safety and immunogenicity of a live recombinant attenuated intranasal HPIV3 vaccine, rHPIV3cp45. This study will last for approximately 28 weeks. Infants and children 6 months to 36 months of age will be randomly assigned to one of two groups. Group 1 participants will receive 2 immunizations of rHPIV3cp45. Group 2 participants will receive 2 doses of rHPIV3cp45 placebo. Immunizations will be given as nose drops and administered at study entry and approximately 22 to 27 weeks after study entry. On the day of immunization, a physical exam and blood collection will occur. Participants will be observed for 15 minutes after immunization for any immediate adverse effects. Parents or guardians will be given a thermometer to take with them and will be instructed on how to take their child's temperature. They will be given the study schedule and will need to provide contact phone numbers so study personnel can contact them by phone during the days after immunization. Parents and guardians will be contacted by telephone daily from Day 1 to Day 18 after each immunization. Parents or guardians will need to record their child's temperature daily for at least 17 days immediately following immunization. During this 17-day period, study visits will occur on Days 3, 6, and 12 after each dose of vaccine or placebo. Participants will undergo a nasal wash for a viral culture at all study visits. There will be additional follow-up visits occurring sometime between 49 and 63 days after the first dose and 28 to 35 days after the second dose; blood collection will occur at the follow-up visits. Additional visits may be required on selected days during the month after immunization. Infants who experience illness or side effects may be asked to return to the clinic for examination.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

PREVENTION

Masking

TRIPLE

Enrollment

Conditions

Paramyxoviridae Infections Virus Diseases

Interventions

rHPIV3cp45DRUG

10\^5 TCID50 nasal drops

rHPIV3cp45 placeboDRUG

1X-L15 nasal drops

Eligibility

Sex: ALLMin age: 6 MonthsMax age: 36 MonthsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Good general health * HPIV3-uninfected * Has received age-appropriate inactivated or subunit routine immunizations at least 2 weeks prior to study entry * Has received age-appropriate live routine immunizations at least 4 weeks prior to study entry and at least 2 weeks for rotavirus and inactivated vaccines * Available for the duration of the trial * Parent or guardian reachable by telephone for post-immunization contact * Parent or guardian willing to provide informed consent Exclusion Criteria: * Known or suspected impairment of immunologic functions. Infants who are HIV-infected, who are bone marrow or solid organ transplant recipients, or who have received immunosuppressive therapy, including systemic corticosteroids within 30 days prior to study entry. Infants who are using topical steroids, topical antibiotic ointments and topical antifungal agents are not excluded. * Major congenital malformations, including congenital cleft palate, cytogenetic abnormalities, or serious chronic disorders * Previously received HPIV3 vaccine * Previous serious vaccine-associated adverse event or anaphylactic reaction * Known hypersensitivity to any vaccine component * Lung or heart disease, including reactive airway disease. Infants with clinically insignificant cardiac abnormalities are not excluded. Infants or children who wheezed once or received bronchodilator therapy once in the first year of life but who have not had any additional wheezing episodes or bronchodilator therapy for at least 12 months are not excluded. * Born prematurely before the 37th week of pregnancy if participant is currently less than 12 months of age * Member of a household containing immunocompromised individuals, pregnant caregivers, or infants less than 6 months of age * Attends day care with infants less than 6 months of age * Parent or guardian unable or unwilling to suspend daycare for 14 days following each immunization. More information on this criterion can be found in the protocol. * Enrolled in another investigational drug or vaccine study from 30 days prior to study entry until the final follow-up blood draw

Locations (2)

Center for Immunization Research (CIR), Johns Hopkins School of Public Health

Baltimore, Maryland, United States

Seattle Children's Hospital

Seattle, Washington, United States

Outcomes

Primary Outcomes

Frequency of vaccine-related reactogenicity events and other adverse events

Time frame: Throughout study

Amount of serum antibody induced by vaccine in each recipient

Time frame: Throughout study

Secondary Outcomes

Amount of vaccine virus shed by each recipient

Time frame: Throughout study

Immunogenicity of a second dose of vaccine and the protection of the first dose against re-infection with the second dose

Time frame: From Weeks 22 to 28

Number of vaccinated infants infected with rHPIV3cp45

Time frame: Throughout study

Number of vaccinated participants infected with a second dose of rHPIV3cp45

Time frame: From Weeks 22 to 28

Phenotypic stability of vaccine virus shed

Time frame: Throughout study

Data from ClinicalTrials.gov

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