V260 Registration Study (V260-013)(COMPLETED)

Status Completed

Clinical Trial Summary

Immunogenicity and Safety of V260 in Healthy Infants in Korea

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention

Related Conditions & MeSH terms

Rotavirus

Clinical Trial Details

NCT number	NCT00166517
Study type	Interventional
Source	Merck Sharp & Dohme Corp.
Contact
Status	Completed
Phase	Phase 3
Start date	August 2005
Completion date	July 2006

View Details

See also
Status	Clinical Trial	Phase
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Completed	`NCT00496054` - Safety,Tolerability and Immunogenicity of Vaccination With Rotateq in Healthy Infants in India (V260-021)	Phase 3
Completed	`NCT03587389` - Response to Rotavirus Vaccine in Infants in Ho Chi Minh City in Vietnam	Phase 4
Unknown status	`NCT02177799` - Surveillance Study of Acute Gastroenteritis in Hospitalized Children in Rural Area in Lebanon	N/A
Completed	`NCT01871038` - Rotarix Vaccine Effectiveness	N/A
Completed	`NCT03031743` - The Influence of the Microbiome on Rotavirus Vaccine Immunogenic Response in Infants in Karachi, Pakistan	N/A
Terminated	`NCT00836498` - A Study of the Safety and Immune Response to RotaTeq™ Vaccine in the Elderly (V260-027)	Phase 1
Completed	`NCT02141204` - Immunogenicity, Reactogenicity and Safety Study of Two Different Formulations of GSK Biologicals' Human Rotavirus Vaccine, Rotarix, in Healthy Infants	Phase 3
Enrolling by invitation	`NCT02153866` - The Safety and Immunogenicity Study of Rotavirus Vaccine Simultaneously Vaccinated With MR or MMR Vaccine	Phase 4
Completed	`NCT00820261` - Molecular Epidemiology of Rotavirus Diarrhea Among Infants and Young Children Attending Maua Methodist Hospital, Kenya	N/A
Completed	`NCT00718237` - Phase III Placebo-controlled Study of V260 (RotaTeq™) in Japanese Healthy Infants (V260-029)(COMPLETED)	Phase 3