Study ID

217744/086

Clinical Study ID

217744/086 (DTPa-HBV-IPV-086)

Study Title Single-blind, multicentre, phase IV clinical trial to assess and compare the immunogenicity and reactogenicity of GSK Biologicals’ DTPa-HBV-IPV/Hib vaccine (Infanrix hexa™) and Aventis Pasteur’s DTPa-HBV-IPV-Hib vaccine (Hexavac™) given as a primary vaccination course at 2, 4 and 6 months of age.
Patient Level Data Study Listed on ClinicalStudyDataRequest.com
Clinicaltrials.gov Identifier
Sponsor GlaxoSmithKline
Collaborators N/A
Phase Phase 4
Study Recruitment Status Completed
Generic Name Combined Diphtheria, Tetanus, Acellular Pertussis, Hepatitis B, Inactivated Polio, Haemophilus influenzae Type b Vaccine
Trade Name Infanrix Hexa
Study Indication Diphtheria; Haemophilus influenzae type b; Hepatitis B; Poliomyelitis; Tetanus; acellular pertussis

For more information on this register please email GSKClinicalSupportHD@gsk.com

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GSK-sponsored clinical trials are those for which GSK is ultimately responsible for all aspects of the study even if some or all of these activities are transferred to another party.

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