MedPath

Small Study of TT Vaccine

Phase 1
Registration Number
CTRI/2017/11/010448
Lead Sponsor
Biovaccines INDIA
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Healthy Adult Subjects

Exclusion Criteria

NOT WILLING TO GIVE CONSENT

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Proportion/percentage of subjects achieving seroconversion response against tetanus vaccine, 4 weeks after single booster doseTimepoint: Proportion/percentage of subjects achieving seroconversion response against tetanus vaccine, 4 weeks after single booster dose
Secondary Outcome Measures
NameTimeMethod
â?¢Incidence of solicited adverse events 7 days after the vaccine dose in the two treatment groupsTimepoint: 4 WEEKS
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