| 1 |
Human subjects of either gender between 18–55 y age. |
1 |
History of animal bite in the past |
| 2 |
Subjects likely to be available for all visits during follow-up period. |
2 |
Pregnancy and lactation |
| 3 |
Subjects willing to sign Informed consent. |
3 |
Subjects have received any type of rabies vaccination in the past. |
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4 |
Subjects have received any type of rabies immunoglobulin (human/equine) in the past. |
| |
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5 |
Subjects suffering from any other illness of whatsoever nature. |
| |
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6 |
Subjects are on steroids or any other immunosuppressant or known to be HIV positive. |
| |
|
7 |
Subjects are on concomitant antimalarials. |
| |
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8 |
Subjects with history of allergy to any ingredient of the vaccine. |
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9 |
Participation in another clinical trial in the past 3 mo |
