- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02601612
Safety and Immunogenicity of the RSV D46cpΔM2-2 Vaccine in RSV-Seropositive Children and RSV-Seronegative Infants and Children
A Phase I Study of the Safety and Immunogenicity of a Single Dose of the Live Recombinant RSV D46cpΔM2-2 Vero Grown Virus Vaccine (Lot RSV #008A), Delivered as Nose Drops to RSV-Seropositive Children 12 to 59 Months of Age and RSV-Seronegative Infants and Children 6 to 24 Months of Age
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Human RSV is the most common viral cause of serious acute lower respiratory illness (LRI) in infants and children under 5 years of age worldwide. This study will evaluate the safety and immunogenicity of the RSV D46cpΔM2-2 vaccine in RSV-seropositive children and RSV-seronegative infants and children. The vaccine will be evaluated in a stepwise fashion beginning in RSV-seropositive children (Group 1), and then in RSV-seronegative infants and children (Group 2). In each group, participants will be randomly assigned to receive a single dose of D46cpΔM2-2 vaccine or placebo at study entry (day 0).
Participants will be enrolled in the study between April 1 and October 31, outside of the RSV season. Group 1 (RSV-seropositive children) will attend several study visits and will be followed for 28 days. Group 2 (RSV-seronegative infants and children) will remain on study until they complete the post-RSV season visit between April 1 and April 30 in the calendar year following enrollment. Participants in Group 2 will also attend several study visits during the time they are enrolled in the study. Study visits for all participants may include clinical assessments, blood collection, and nasal washes.
Undersøgelsestype
Tilmelding (Forventet)
Fase
- Fase 1
Kontakter og lokationer
Studiesteder
-
-
Maryland
-
Baltimore, Maryland, Forenede Stater, 21205
- Johns Hopkins Bloomberg School of Public Health
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
RSV-Seropositive Children:
Inclusion Criteria:
- Greater than or equal to 12 months of age and less than 60 months of age
- Received routine immunizations appropriate for age
- Serum RSV neutralizing antibody titer greater than or equal to 1:40
- Serum RSV neutralizing antibody result obtained this calendar year
- Pre-inoculation serum RSV neutralizing antibody specimen obtained less than or equal to 56 days prior to inoculation
- Parent/guardian has completed the study comprehension assessment
- Parent/guardian has signed the study informed consent document (ICD)
- Subject is expected to be available for the duration of the study
Exclusion Criteria:
- Evidence of chronic disease
- Within the past 6 months had a decline in height or weight growth that crosses two major growth percentiles (e.g., from above the 75th to below the 25th)
- Known or suspected impairment of immune function
- Maternal history of positive HIV test
- Bone marrow/solid organ transplant recipient
- Major congenital malformations, including congenital cleft palate or cytogenetic abnormalities
- Current or unresolved suspected or documented developmental disorder, delay, or other developmental problem
- Cardiac abnormality requiring treatment
- Lung disease or reactive airway disease
- More than one episode of wheezing in the first year of life
- Wheezing episode or received bronchodilator therapy within the past 12 months
- Previous immunization with an experimental RSV vaccine
- Previous receipt or planned administration of anti-RSV antibody product
- Previous serious vaccine-associated AE or anaphylactic reaction
- Known hypersensitivity to any vaccine component
- Previous receipt of immunoglobulin or any antibody products
- Previous receipt of any other blood products within the past 6 months
- Member of a household that contains an infant who is less than 12 months of age during study days 0 to 10
- Member of a household that includes an immunocompromised individual
- Member of a household that includes a person who has received chemotherapy within the past 12 months
- Will attend a daycare facility that does not separate children by age and contains an infant who is greater than 12 months of age during study days 0 to 10
RSV-Seronegative Infants and Children:
Inclusion Criteria:
- Greater than or equal to 6 months of age and less than 25 months of age
- Received routine immunizations appropriate for age
- Serum RSV neutralizing antibody titer is less than 1:40
- Screening and pre-inoculation serum RSV neutralizing antibody specimen obtained less than or equal to 42 days prior to inoculation
- Parent/guardian has completed the study comprehension assessment
- Parent/guardian has signed the study ICD
- Subject is expected to be available for the duration of the study
- Born at greater than or equal to 37 weeks gestation or is currently greater than 1 year of age
Exclusion Criteria:
- Evidence of chronic disease
- Within the past 6 months had a decline in height or weight growth that crosses two major growth percentiles (e.g., from above the 75th to below the 25th)
- Known or suspected impairment of immune function
- Maternal history of positive HIV test
- Bone marrow/solid organ transplant recipient
- Major congenital malformations, including congenital cleft palate or cytogenetic abnormalities
- Current or unresolved suspected or documented developmental disorder, delay, or other developmental problem
- Cardiac abnormality requiring treatment
- Lung disease or reactive airway disease
- More than one episode of wheezing in the first year of life
- Wheezing episode or received bronchodilator therapy within the past 12 months
- Previous immunization with an experimental RSV vaccine
- Previous receipt or planned administration of anti-RSV antibody product
- Previous receipt of immunoglobulin or any antibody products
- Previous receipt of any other blood products within the past 6 months
- Previous serious vaccine-associated AE or anaphylactic reaction
- Known hypersensitivity to any vaccine component
- Member of a household which contains an infant who is less than 6 months of age during study days 0 to 28
- Member of a household that includes an immunocompromised individual
- Member of a household that includes a person who has received chemotherapy within the past 12 months
- Will attend a daycare facility that does not separate children by age and contains an infant who is less than 6 months of age during study days 0 to 28
Temporary Exclusion Criteria for RSV-Seropositive and RSV-Seronegative Children:
To be eligible to participate, RSV-seropositive and RSV-seronegative infants and children must satisfy none of the temporary exclusion criteria. The following conditions are temporary or self-limiting. Once the condition is resolved and the subject is otherwise eligible, the subject may be enrolled or rescreened, if necessary.
Any of the following events at the time of inoculation:
- fever (rectal temperature of greater than or equal to 100.4°F),
- upper respiratory signs or symptoms (rhinorrhea, cough, or pharyngitis)
- nasal congestion significant enough to interfere with successful inoculation
- otitis media
- Receipt of any killed vaccine or live-attenuated rotavirus vaccine less than 14 days prior to inoculation
Receipt of the following medications less than 28 days prior to inoculation:
- any live vaccine other than rotavirus
- another investigational vaccine or investigational drug,
- systemic corticosteroids administered for greater than 14 days at a dosage equivalent to prednisone at greater than 2 mg/kg or 20 mg daily
- salicylate (aspirin) or salicylate-containing products
Receipt of a non-permitted concomitant medication or any of the following medications less than 3 days prior to inoculation:
- systemic antibacterial, antiviral, antifungal, anti-parasitic, or antituberculous agents, whether for treatment or prophylaxis,
- intranasal medications
Scheduled administration of the following in relation to planned inoculation:
- killed vaccine within the 14 days following,
- any live vaccine other than rotavirus within the 28 days following,
- another investigational vaccine or drug within the 28 days following for RSV-seropositive children and the 56 days following for RSV-seronegative infants and children
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Firedobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Eksperimentel: Group 1: D46cpΔM2-2 Vaccine
RSV-seropositive children will receive a single dose of 10^6 PFU D46cpΔM2-2 vaccine at study entry (day 0).
|
Delivered as nose drops
|
Placebo komparator: Group 1: Placebo
RSV-seropositive children will receive a single dose of placebo at study entry (day 0).
|
Leveres som næsedråber
|
Eksperimentel: Group 2: D46cpΔM2-2 Vaccine
RSV-seronegative infants and children will receive a single dose of 10^5 PFU D46cpΔM2-2 vaccine at study entry (day 0).
|
Delivered as nose drops
|
Placebo komparator: Group 2: Placebo
RSV-seronegative infants and children will receive a single dose of placebo at study entry (day 0).
|
Leveres som næsedråber
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
---|---|
Frequency of vaccine-related solicited adverse events (AEs) that occur during the acute monitoring phase of the study
Tidsramme: Measured at days 0-10 for seropositive and days 0-28 for seronegative
|
Measured at days 0-10 for seropositive and days 0-28 for seronegative
|
Severity of vaccine-related solicited AEs that occur during the acute monitoring phase of the study
Tidsramme: Measured at days 0-10 for seropositive and days 0-28 for seronegative
|
Measured at days 0-10 for seropositive and days 0-28 for seronegative
|
Frequency of vaccine-related lower respiratory illness
Tidsramme: Measured during study days 0-28 for seropositive subjects and study days 0-56 for seronegative subjects
|
Measured during study days 0-28 for seropositive subjects and study days 0-56 for seronegative subjects
|
Proportion of subjects shedding vaccine virus
Tidsramme: Measured during study days 0-28 for seropositive subjects and study days 0-56 for seronegative subjects
|
Measured during study days 0-28 for seropositive subjects and study days 0-56 for seronegative subjects
|
Proportion of subjects that develop 4-fold or greater increases in RSV neutralizing antibody titer following vaccination
Tidsramme: Measured during study days 0-28 for seropositive subjects and study days 0-56 for seronegative subjects
|
Measured during study days 0-28 for seropositive subjects and study days 0-56 for seronegative subjects
|
Samarbejdspartnere og efterforskere
Efterforskere
- Ledende efterforsker: Ruth A. Karron, MD, Center for Immunization Research (CIR), Johns Hopkins Bloomberg School of Public Health (JHSPH)
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- CIR 308
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Respiratoriske syncytielle virusinfektioner
-
NovavaxAfsluttetRespiratorisk syncytial virus (RSV)Forenede Stater
-
MedImmune LLCAfsluttetRespiratorisk syncytial virus (RSV)Forenede Stater
-
AbbVieAfsluttet
-
University of RochesterAktiv, ikke rekrutterendeRespiratorisk syncytial virus (RSV)Forenede Stater
-
University of OxfordInnovative Medicines Initiative; Respiratory syncytial virus consortium...Aktiv, ikke rekrutterendeRespiratorisk syncytial virus (RSV)Det Forenede Kongerige
-
Enanta Pharmaceuticals, IncAfsluttetRespiratorisk syncytial virus (RSV)Forenede Stater
-
GlaxoSmithKlineAfsluttetRespiratorisk syncytial virus (RSV)Belgien
-
NovavaxPATHAfsluttetRespiratorisk syncytial virus (RSV)Forenede Stater
-
National Institute of Allergy and Infectious Diseases...Aktiv, ikke rekrutterendeRespiratorisk syncytial virus (RSV)Forenede Stater
-
Enanta Pharmaceuticals, IncRekrutteringRespiratorisk syncytial virus (RSV)Forenede Stater, Spanien, Israel, Australien, Tyskland, Korea, Republikken, Taiwan, Det Forenede Kongerige, Argentina, Brasilien, New Zealand, Polen, Rumænien, Sydafrika, Mexico
Kliniske forsøg med Placebo
-
SamA Pharmaceutical Co., LtdUkendtAkut bronkitis | Akut øvre luftvejsinfektionKorea, Republikken
-
National Institute on Drug Abuse (NIDA)AfsluttetBrug af cannabisForenede Stater
-
AstraZenecaParexel; Spandauer Damm 130; 14050; Berlin, GermanyAfsluttetMandlige forsøgspersoner med type II-diabetes (T2DM)Tyskland
-
Heptares Therapeutics LimitedAfsluttetFarmakokinetik | SikkerhedsproblemerDet Forenede Kongerige
-
Texas A&M UniversityNutraboltAfsluttetGlucose and Insulin Response
-
Longeveron Inc.AfsluttetHypoplastisk venstre hjerte syndromForenede Stater
-
Regado Biosciences, Inc.AfsluttetSund frivilligForenede Stater
-
ItalfarmacoAfsluttetBeckers muskeldystrofiHolland, Italien
-
West Penn Allegheny Health SystemAfsluttetAstma | Allergisk rhinitisForenede Stater