Investigating the Immunogenicity of a U.S.-Licensed Meningococcal Serogroup B Vaccine (Trumenba)

PHASE4CompletedINTERVENTIONAL
Enrollment

18

Participants

Timeline

Start Date

January 31, 2015

Primary Completion Date

December 31, 2016

Study Completion Date

December 31, 2016

Conditions
Meningococcal Infections
Interventions
BIOLOGICAL

Trumenba Vaccine (Wyeth/Pfizer Pharmaceuticals)

All subjects will receive three doses of a Trumenba, a U.S.-licensed meningococcal vaccine. Each 0.5 mL dose contains 60 micrograms of each FHbp variant (total of 120 micrograms of protein), 0.018 mg of PS80 and 0.25 mg of Al³+ as AlPO4 in 10 mM histidine buffered saline at pH 6.0. Trumenba is administered as a three dose series (0.5 mL each) according to a 0-, 2-, and 6-month schedule.

Trial Locations (2)

94609

UCSF Benioff Children's Hospital Oakland, Oakland

01655

University of Massachusetts Medical School, Worcester

All Listed Sponsors
collaborator

University of Massachusetts, Worcester

OTHER

lead

UCSF Benioff Children's Hospital Oakland

OTHER

NCT02569632 - Investigating the Immunogenicity of a U.S.-Licensed Meningococcal Serogroup B Vaccine (Trumenba) | Biotech Hunter | Biotech Hunter