MedPath

A comparison of safety and immunogenicity between government of India approved Rabies pre exposure prophylaxis regimen and WHO Rabies pre exposure prophylaxis regime

Phase 3
Registration Number
CTRI/2023/09/057399
Lead Sponsor
Dr N R Ramesh Masthi
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

•Healthy subjects willing to volunteer and sign written informed consent for the study.

•Subjects should be available for the follow-up period.

Exclusion Criteria

?Received Anti rabies vaccine or RIG or RMAb anytime in the past.

?Participation in any other clinical trial in the past three months.

?Severely immunocompromised subjects, pregnant and lactating women.

Subjects with known history of allergy.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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