2015-001485-26
Study to evaluate the efficacy, safety and immunogenicity of two or three doses of GSK Biologicals’ oral live attenuated human rotavirus (HRV) vaccine given concomitantly with routine EPI vaccinations in healthy infants.
GlaxoSmithKline Biologicals·EU Clinical Trials Register
Study focus
- Disease/Condition
- Healthy volunteers
Sponsor & location
- Primary sponsor
- GlaxoSmithKline Biologicals
Timeline & enrollment
- Phase
- N/A
- Start date
- N/A
- End date
- N/A
Primary outcome
Occurrence of severe RV GE (score > 11 on a 20-point Vesikari scoring system caused by the circulating wild-type RV strains in pooled HRV groups versus the placebo group.
ICD-10 classifications
Healthy person accompanying sick personRoutine general health check-up of armed forcesRoutine general health check-up of sports teamsRoutine general health check-up of inhabitants of institutions
Data source
- Registry
- EU Clinical Trials Register
- Trial ID
- 2015-001485-26
- Type
- Non-Device Trial
About this record
Access comprehensive clinical trial information for 2015-001485-26 through Pure Global AI's free database. This phase not specified trial is sponsored by GlaxoSmithKline Biologicals and is currently status unknown. The study focuses on Healthy volunteers.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to EU Clinical Trials Register data, helping medical device and pharmaceutical companies navigate clinical research efficiently.