Skip to content

A post licensure clinical trial to assess the safety and tolerability of BE’s Measles-Rubella vaccine in 9 to 12 months old healthy infants in a single dose.

A multicentre single arm non-comparative Phase-IV post marketing study to evaluate the safety and tolerability of Biological E’s Live, Attenuated Measles-Rubella Vaccine (MR) in 9-12 month old Healthy Infants. - None

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
CTRI
Registry ID
CTRI/2019/04/018683
Enrollment
1000
Registered
2019-04-22
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: Z23- Encounter for immunization

Interventions

Intervention1: Measles and Rubella (MR) Vaccine, (Live), (Attenuated,Freeze-dried) of BE Ltd.: BE’s live attenuated Measles-Rubella vaccine 0.5 mL per dose to be administered subcutaneously on day 0.

Sponsors

Biological ELimited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Healthy infants of either gender between 9-12 months of age at the time of first vaccination; 2. Infants free of obvious health problems as established by medical history and physical examination before entering the study. 3. Parent or LAR willing to provide written informed consent. 4. Willing to strictly follow the study protocol requirements.

Exclusion criteria

Exclusion criteria: 1. Serious adverse event to any earlier vaccinations, as respiratory difficulty, angioedema and anaphylaxis; 2. History of Measles, MR or MMR vaccination(s) 3. Family history of any hypersensitivity reactions to Measles, MR or MMR vaccination(s) or allergy to any of their components. 4. Acute or chronic illness or major congenital defects; 5. Exposure to measles and rubella =30 days before study start; 6. Use of blood products within 3 months before the vaccination; 7. Use of any unregistered vaccine type within 30 days before the study vaccination ; 8. Use of any kind of investigational medication within 3 months before the study vaccination; 9. Coagulopathies diagnosed by a physician or report of capillary fragility (ex: bruises or bleedings without justifiable cause); 10. A history of neurologic disorders or seizures; 11. Any criteria, which in the opinion of the Investigator, suggests that the child would not be compliant with the requirements of the study protocol.

Design outcomes

Primary

MeasureTime frame
Number and percentage of: 1.solicited local and systemic adverse events (AEs). 2. solicited local and systemic AEs 3. unsolicited AEs 4. Rate of SAEs and medically attended AEs 5. Number and percentage of subjects with clinically significant abnormal vital signs (Pulse, Axillary body temperature and Respiratory rate)Timepoint: 1. During first 30 minutes of post-vaccine administration. 2. during subsequent 14-day (Day 0-13) post vaccination period, captured through subject diary. 3. up to day 42 after the vaccination. 4. until day 42 after the vaccination. 5. at each visit.

Secondary

MeasureTime frame
NoneTimepoint: None

Countries

India

Contacts

Public ContactDr Subhash Thuluva

Biological E.Limited

subhash.thuluva@biologicale.com04071216000

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 9, 2026