Salmonella Conjugates CVD 1000: Study of Responses to Vaccination With Trivalent Invasive Salmonella Disease Vaccine

PHASE1CompletedINTERVENTIONAL
Enrollment

96

Participants

Timeline

Start Date

October 28, 2019

Primary Completion Date

May 7, 2021

Study Completion Date

May 7, 2021

Conditions
Risk Reduction
Interventions
BIOLOGICAL

Trivalent Invasive Salmonella Disease Vaccine (6.25 µg)

6.25 µg of the conjugate vaccine is administered via one intramuscular injection into the deltoid muscle on Study Day 1.

BIOLOGICAL

Trivalent Invasive Salmonella Disease Vaccine (12 µg)

12 µg of the conjugate vaccine is administered via one intramuscular injection into the deltoid muscle on Study Day 1.

BIOLOGICAL

Trivalent Invasive Salmonella Disease Vaccine (25 µg)

25 µg of the conjugate vaccine is administered via one intramuscular injection into the deltoid muscle on Study Day 1.

BIOLOGICAL

Trivalent Invasive Salmonella Disease Vaccine (highest, well-tolerated dose among Cohorts A-C)

The highest, well-tolerated dose of the conjugate vaccine among Cohorts A-C is administered via one or two intramuscular injection(s) into the deltoid muscle on Study Day 1 (and 29 if two doses are given).

OTHER

Placebo

0.5 mL of buffer and preservative is administered via one or two intramuscular injections(s) into the deltoid muscle on Study Day 1 (and 29 if two doses are given).

Trial Locations (1)

21201

University of Maryland, Baltimore, Center for Vaccine Development and Global Health, Baltimore

All Listed Sponsors
lead

University of Maryland, Baltimore

OTHER

NCT03981952 - Salmonella Conjugates CVD 1000: Study of Responses to Vaccination With Trivalent Invasive Salmonella Disease Vaccine | Biotech Hunter | Biotech Hunter