A clinical study to assess the safety and immunogenicity of liquid DTwP-rHepB-HIB-IPV vaccine when administered in healthy infants of 6-8 weeks.
- Conditions
- Health Condition 1: Z23- Encounter for immunization
- Registration Number
- CTRI/2024/02/063223
- Lead Sponsor
- Ms Biological E Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- Not specified
- Target Recruitment
- 0
1. Intended subjects will be healthy infants between 6-8 weeks of age, of either gender at the time of 1st vaccination.
2. Written or thumb printed informed consent obtained from the subject’s parent(s) or legally acceptable representative prior to performing any study specific procedure.
3. Healthy infants with weight = 3300gms at the time of 1st vaccination.
4. Good clinical condition established by medical history and physical examination (with no acute disease, infection or high temperature).
5. Subjects and or their mothers not participating in any other clinical trials.
6. Infants without contraindications or precautionary circumstances for participating in the trial.
7. Ability of the subject’s parent or legally acceptable representative or guardian to understand and comply with the requirements of the protocol (e.g. completion of the diary cards, return for follow-up visits).
1. Child in care
2. Prior immunization with DTP, Hepatitis-B or HIB vaccine with the exception of birth dose BCG, Hepatitis B & oral polio vaccine.
3. Co-administration of any oral or injectable polio vaccine during the course of the study.
4. Current illness (especially fever) or any acute or congenital illness or disability.
5. Evidence of previous or intercurrent diphtheria, tetanus, pertussis, hepatitis B, poliomyelitis and or H. influenzae type b diseases
6. Subjects receiving immunosuppressive therapy.
7. Known or suspected allergy to any of the vaccine components.
8. Any sign or symptom or systemic dysfunction, especially of the central nervous system (CNS).
9. Known family history of SIDS (Sudden Infant Death Syndrome).
10. Planned or elective surgery during the course of the study.
11. Infants who have received any blood products, any dose of corticosteroids, cytotoxic agents or radiotherapy.
12. Subjects and or their mothers who have participated in another clinical trial of an investigational agent within last 30 days or likely to participate during the study course.
13. Inability or unwillingness to abide by the requirements of the protocol.
14. Any medical condition that in the judgment of the investigator would make intramuscular injection unsafe.
15. Any criteria, which in the opinion of the Investigator, suggests that the subject would not be compliant with the study protocol.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method