Phase II, Double-blind, Randomized, Placebo-controlled Study of 2 Doses of GSK Biologicals' Live Attenuated Human Rotavirus Vaccine at Different Virus Concentrations (10 5.2 and 10 6.4 Ffu) in Healthy Infants Following a 0, 2 Month Schedule and Previously Uninfected With Human Rotavirus.

GlaxoSmithKline0 sites529 target enrollmentNovember 2000

ConditionsInfections, Rotavirus

Overview

Phase: Phase 2
Intervention: Not specified
Conditions: Infections, Rotavirus
Sponsor: GlaxoSmithKline
Enrollment: 529
Primary Endpoint: Proportion of subjects with vaccine take
Status: Completed
Last Updated: 9 years ago

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

This is a dose exploration study to assess the safety and immunogenicity of two doses of the candidate HRV vaccine at different virus concentrations in the target age group (infants approximately 2 months of age and previously uninfected with human rotavirus) and receiving concomitant administration of routine vaccinations. The study also aims at exploring the effect of unrestricted feeding on the immunogenicity of the vaccine.

Detailed Description

All subjects enrolled from Eastern United States and Eastern Canada will continue their participation in the pilot efficacy follow-up (pilot efficacy subset). The third dose of IPV vaccine (IPOL) may be given at visit 3, 4 or another time, at the investigator's discretion. Comvax may be given in place of OmniHIB/ActHIB at Visit 1 and Visit 2 and the third dose of Comvax administered according to the prescribing information.

Registry

clinicaltrials.gov

Start Date

November 2000

End Date

September 2002

Last Updated

9 years ago

Study Type

Interventional

Study Design

Parallel

Sex

All

Investigators

Sponsor

GlaxoSmithKline

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

•A male or female child between, and including 6 and 12 weeks (42-90 days) of age at the time of the first vaccination.
•Free of obvious health problems as established by medical history and clinical examination before entering into the study.
•Written informed consent obtained from the parents or guardians of the subject.
•Born after a normal gestation period (between 36 and 42 weeks).

Exclusion Criteria

•Use of any investigational or non-registered drug or vaccine other than the study vaccine within 30 days preceding the study vaccine or placebo or planned use during the study period.
•Planned administration of a vaccine (including routine pediatric vaccines) not foreseen by the study protocol during the period starting from 14 days before each dose of vaccine(s) and ending 14 days after. Hepatitis B vaccine given concomitantly or within 14 days before and after vaccination is not an exclusion criteria.
•Chronic administration (defined as more than 14 days) of immunosuppressants or other immune-modifying drugs since birth.
•History of diphtheria, tetanus, pertussis, polio, Hib disease and/or invasive pneumococcal infection. History of invasive pneumococcal infection is not an exclusion criteria for Canadian subjects.
•Previous vaccination against diphtheria, tetanus, pertussis, polio, Haemophilus influenzae type b, and/or Streptococcus pneumoniae. Previous vaccination against Streptococcus pneumoniae is not an exclusion criteria for Canadian subjects.
•Use of antibiotics within 7 days preceding dose
•Any clinically significant history of chronic gastrointestinal disease including any uncorrected congenital malformation of the GI tract or other serious medical condition as determined by the investigator.
•Any confirmed or suspected immunosuppressive or immunodeficient condition, including human immunodeficiency virus (HIV) infection.
•History of allergic disease or reaction likely to be exacerbated by any component of the vaccine.
•Acute disease at time of enrollment.

Outcomes

Primary Outcomes

Proportion of subjects with vaccine take

Time Frame: Two months after the second dose

Occurrence of any grade 2 or 3 fever, vomiting or diarrhea

Time Frame: Within the 15-day solicited follow-up period after any dose of study vaccine.

Secondary Outcomes

Anti-PRP, anti-diphtheria, anti-tetanus, anti-polio type 1, 2 and 3 seroprotection status.(Two months after dose 2 and at the end of the study.)
Occurrence of each type of solicited symptoms(Within the 15-day solicited follow-up period after any dose of study vaccine)
Occurrence of unsolicited symptoms according to WHO classification.(Within 42 days after dose 1 and dose 2)
Occurrence of serious adverse events(Throughout the entire study period)
Serum rotavirus immunoglobulin A (IgA) antibody titers(At visits 1, 3 and 4 and at all Visits for pilot efficacy subset)
Rotavirus seropositivity status(Before dose 1 and at the end of the study)
Vaccine take (for pilot efficacy subset only)(2 months after dose 1)
Anti- polyribosyl-ribitol phosphate (PRP), anti-diphtheria and anti-tetanus toxoids, anti- pertussis toxoid (PT), anti- filamentous haemagglutinin (FHA), anti- pertactin (PRN), anti-polio type 1, 2 and 3 antibody concentrations(Two months after dose 2 and at the end of the study.)
Antibody concentrations to pneumococcal serotypes 4, 6B, 9V, 14, 18C, 19F and 23F(Two months after dose 2 and at the end of the study (only in a subset of U.S. subjects))
Anti-PT, anti-FHA, anti-PRN, pneumococcal serotypes 4, 6B, 9V, 14, 18C, 19F and 23F (only in US subjects) seropositivity status.(Two months after dose 2 and at the end of the study.)
Seropositivity status and Geometric mean titres (GMTs) of rotavirus IgA for breast fed infants compared with formula fed infants(Two months after dose 2.)
Occurrence of rotavirus gastroenteritis (in a pilot efficacy subset of subjects)(Two weeks after dose 2 until the end of the rotavirus season following vaccination.)