Status:
COMPLETED
Study of Purified Vero Rabies Vaccine Compared With a Reference Rabies Vaccine as Simulated Rabies Post-Exposure Prophylaxis in Adult and Pediatric Population in Thaïland
Lead Sponsor:
Sanofi Pasteur, a Sanofi Company
Conditions:
Rabies (Healthy Volunteers)
Eligibility:
All Genders
1+ years
Phase:
PHASE3
Brief Summary
Primary Objective: To describe the immune response induced by VRVg-2 and Verorab vaccine at Day 14 (to assess the immune response after 3 doses \[2-2-2\]) and Day 42 (to assess the immune response af...
Detailed Description
The duration of each participant's participation in the study is approximately 7 months (28 day-vaccination period followed by 6 month safety follow-up period).
Eligibility Criteria
Inclusion
- Inclusion criteria :
- Aged ≥ 1 year on the day of inclusion
- Participant (adult ≥ 18 years without upper age limit) or participant and participant's parent/LAR (child ≥ 1 to \< 18 years) are able to attend all scheduled visits and to comply with all study procedures
- The following criterion only applies to healthy adults ≥ 18 years:
- \- Body Mass Index (BMI): 18.5 kg/m2 ≤ BMI ≤ 30 kg/m2
Exclusion
- Exclusion criteria:
- Pregnant, or lactating, or of childbearing potential and not using an effective method of contraception or abstinence from at least 4 weeks prior to the first vaccination and until 1 month after each vaccination. To be considered of non-childbearing potential, a female must be pre-menarche or post-menopausal for at least 1 year, or surgically sterile.
- Participation at the time of study enrollment or, planned participation during the present study period in another clinical study investigating a vaccine, drug, medical device, or medical procedure
- Receipt of any vaccine in the 4 weeks (28 days) preceding the first study vaccination or planned receipt of any vaccine prior to Visit 8 (D90)
- Previous vaccination against rabies (in pre- or post-exposure regimen) with either the study vaccines or another vaccine
- Bite by, or exposure to a potentially rabid animal in the previous 6 months without post-exposure prophylaxis
- Receipt of immune globulins, blood or blood-derived products in the past 3 months
- Known or suspected congenital or acquired immunodeficiency; or receipt of immunosuppressive therapy, such as anti-cancer chemotherapy or radiation therapy, within the preceding 6 months; or long-term systemic corticosteroid therapy (prednisone or equivalent for more than 2 consecutive weeks within the past 3 months)
- At high risk for rabies exposure
- Known systemic hypersensitivity to any of the study/control vaccine components or, for adults, to ERIG Group 3 and Group 4) or HRIG (Group 5 and Group 6), or history of a life-threatening reaction to the vaccines used in the study or to a vaccine containing any of the same substances
- Positive skin test to ERIG at Visit 1 for only adult participants enrolled in Group 3 and Group 4 as per superseded Protocol version 5.0
- Self-reported thrombocytopenia
- Bleeding disorder, or receipt of anticoagulants in the 3 weeks preceding inclusion
- Deprived of freedom by an administrative or court order, or in an emergency setting, or hospitalized involuntarily
- Current alcohol or substance abuse that, in the opinion of the Investigator, might interfere with the study conduct or completion
- Chronic illness that, in the opinion of the Investigator, is at a stage where it might interfere with study conduct or completion
- Moderate or severe acute illness/infection (according to Investigator judgment) on the day of vaccination or febrile illness (temperature ≥ 38.0 C). A prospective subject should not be included in the study until the condition has resolved or the febrile event has subsided
- Personal history of Guillain-Barré syndrome
- Identified as an Investigator or employee of the Investigator or study center with direct involvement in the proposed study, or identified as an immediate family member (ie, parent, spouse, natural or adopted child) of the Investigator or employee with direct involvement in the proposed study
- Receipt of chloroquine or hydroxychloroquine up to 2 months prior to the study or through to study until Visit 8
- The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Key Trial Info
Start Date :
August 4 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 21 2022
Estimated Enrollment :
403 Patients enrolled
Trial Details
Trial ID
NCT04478084
Start Date
August 4 2020
End Date
July 21 2022
Last Update
September 19 2025
Active Locations (3)
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1
Investigational Site Number :7640004
Bangkok, Thailand, 10400
2
Investigational Site Number :7640002
Bangkok, Thailand
3
Investigational Site Number :7640003
Khon Kaen, Thailand, 40002