Clinical Trial for Measles - Rubella Combined Vaccine (MRVAC) Produced by POLYVAC (Phase III)

NCT ID: NCT03713359

Last Updated: 2018-10-19

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE3
• Total Enrollment: 756 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-04-30
• Study Completion Date: 2016-11-30

Brief Summary

The study is conducted to evaluate the safety and Immunogenicity of Measles-Rubella combined vaccine MRVAC produced by POLYVAC (phase 3) on Vietnamese volunteers and to demonstrate non-inferiority on the immunogenicity of MRVAC in comparison to MR vaccine produced by Serum Institute, India.

Detailed Description

A phase III, Randomized, control study to compare the immunogenicity and safety of MRVAC vaccine produced by POLYVAC with MR vaccine licensed in Vietnam produced by Serum Institute, India.

1. Evaluate the safety of MRVAC produced by POLYVAC on Healthy Vietnamese volunteers from 1 - 45 years old.

Evaluate the safety by the ratio of participants having following symptom/signs:

• The ratio of immediate adverse events (local adverse events and systemic adverse events), within 30 minutes after vaccination.
• The ratio of participants having local and systemic adverse events (including unexpected adverse events) occur within 28 days after vaccination.
• The ratio of serious adverse events (SAEs) occur from day 0 to day 28 after vaccination. (SAEs).

2. Evaluate the immunogenicity of MRVAC produced by POLYVAC on the healthy volunteers from 1 - 45 years.

• The rate of sero-conversion;
• GMT (Geomatric mean Antibody titer) after vaccination.

3. Comparison the safety and immunogenicity between MRVAC and control vaccine.

Conditions

Signs and Symptoms

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: SINGLE

Study Groups

Trial arm (MRVAC)

Measles and Rubella combined vaccine (lyophilized) MRVAC produced by POLYVAC is live attenuated measles vaccine. Each vial of 10 doses of measles-rubella combined vaccine is reconstituted with 5.5 mL of water for injection. Each single dose 0.5 mL contains the following components:

Live, attenuated strain AIK-C measles virus not less than 1000 PFU Live, attenuated strain Takahashi rubella virus not less than 1000 PFU Subcutaneous injection

Group Type: ACTIVE_COMPARATOR

Trial arm (MRVAC)

Intervention Type: BIOLOGICAL

Volunteers from 1-45 years old will be injected only one dose of MRVAC vaccine

Control arm

Measles and Rubella combined vaccine produce by Serum Institute, India (lyophilized) is live attenuated Measles and Rubella vaccines being used in the Vietnam expanded immunization program was used as control arm.

Subcutaneous injection

Group Type: ACTIVE_COMPARATOR

Control arm

Intervention Type: BIOLOGICAL

Volunteers from 1-45 years old will be injected only one dose of MRVAC vaccine

Interventions

Trial arm (MRVAC)

Volunteers from 1-45 years old will be injected only one dose of MRVAC vaccine

Intervention Type: BIOLOGICAL

Control arm

Volunteers from 1-45 years old will be injected only one dose of MRVAC vaccine

Intervention Type: BIOLOGICAL

Eligibility Criteria

Inclusion Criteria

• For children 1-2 years old: All subjects must meet all of the following criteria at the time of enroll to stduy:

• Healthy children from 1 year to 2 years old.
• Full-term birth: Pregnancy ≥ 37 weeks.
• Weight at birth is at least 2.5kg.
• Do not get any disease through a clinical examination and ask for medical history before taking part in the study (according to the prescribed information).
• Have not injected Rubella vaccine or a combination vaccine containing Rubella vaccine.
• Have not infected by Rubella before.
• Parents or legal guardians agree to voluntarily consent to their child's participation in the study. Parent or legal guardian is provided basic information about the vaccine as well as benefits, obligations and meaning of participating in the trial. There must be a written consent form for your child to participate.
• For people from 1 year to 45 years old:

• Do not get any disease through a clinical examination and ask for medical history before taking part in the study (according to the prescribed card).
• Have not infected by Rubella before.
• For people over 2 years old up to 18 years old: Parents or legal guardians agree to voluntarily consent to their child's participation in the study. Parent or legal guardian is provided basic information about the vaccine as well as benefits, obligations and meaning of participating in the trial. There must be a written consent form for your child to participate.
• For people aged 18 to 45: Completely volunteering to participate in the study after having been provided with basic information about the trial vaccine as well as the benefits, obligations and meaning of the trial participation. Must sign in the consent form to participate in the study.

Exclusion Criteria

• Fever within 3 days before vaccination (body temperature ≥ 38 degrees Celsius) Persons with congenital malformations, neurological disorders, psychiatric disorders or families with neurological or psychiatric conditions or brain damage.
• Having abnormal immune status or being treated for immunological control; Being immunocompromised as a result of progressive disease treatment.
• Have received immunosuppressive drugs (steroid group) for more than 2 weeks before starting the vaccination.
• Allergy to any vaccine component including hypersensitivity reactions and anaphylactic shock to the antibiotics (Kanamycine and Erythromycin), egg products and gelatin.
• Family history of immunodeficiency.
• Have a history of high fever, seizures
• premature birth (<37 weeks) (applicable to children 1-2 years).
• Malnutrition level 3 or above (applicable to children 1-2 years).
• Have used of gamma globulin, blood transfusions within 3 months before vaccination or gamma glubolin in large doses or the use of immunosuppressive drugs within 6 months before vaccination
• Have used live vaccines within 27 days before vaccination; Have used other vaccines within 4 weeks before entry to study; Use of immunoglobulins or blood products within 3 months before vaccination;
• Is participating in trial other drugs or vaccines; Has an acute or chronic disease that affects the safety (including but not limited to: chronic liver disease, some kidney disease, progressive or unstable neurological disorders, diabetes and organ transplants).
• Having serious acute illness. Responsible doctor or doctor in charge of evaluation consider as unsuitable, such as having abnormal crying ...
• Having plan to go far from the study site between visits. - Being pregnant (for women aged 14 - 45 years)

• Minimum Eligible Age: 12 Months
• Maximum Eligible Age: 45 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Vietnam Military Medical University

OTHER

Sponsor Role: collaborator

Center for Research and Production of Vaccines and Biologicals, Vietnam

OTHER_GOV

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Dinh H. Duong, Ph.D

Role: PRINCIPAL_INVESTIGATOR

Epidemiology department - Vietnam Military Medical University.

Other Identifiers

MRVAC VX.2016.01

Identifier Type: -

Identifier Source: org_study_id