Immunogenicity and Safety of a Purified Vero Rabies Vaccine

Sanofi Pasteur, a Sanofi Company320 enrolled

Overview

This multicenter, observer-blind, controlled, randomized, Phase II study was designed to evaluate different formulations of the Purified Vero Rabies Cell vaccine VRVg.

This study assessed different formulations of the modified formulation of VRVg (VRVg 2- formulations 1 \[low\], 2 \[medium\] and 3 \[high\]) tested in parallel to the initial VRVg formulation (VRVg-1) and Imovax Rabies. Immune responses were assessed at Day 14, Day 28, Day 42, and at Month 7. Safety events were also reported.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

QUADRUPLE

Enrollment

320

Conditions

Rabies Virus

Interventions

VRVg 2BIOLOGICAL

Modified formulation 1 (Low) of Purified Vero Rabies Vaccine Serum Free

VRVg 1BIOLOGICAL

Initial formulation of Purified Vero Rabies Vaccine Serum Free

Imovax RabiesBIOLOGICAL

Purified inactivated rabies vaccine prepared on human diploid cell cultures

Eligibility

Sex: ALLMin age: 18 YearsMax age: 65 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: An individual must fulfill all of the following criteria in order to be eligible for trial enrollment: 1. Aged 18 to less than 65 years on the day of inclusion. 2. Informed consent form had been signed and dated. 3. Able to attend all scheduled visits and to complied with all trial procedures. 4. Body Mass Index (BMI): 18.5 kilograms per meter square (Kg/m\^2) less than or equal to (\<=) BMI \<= 30 Kg/m\^2. Exclusion Criteria: An individual fulfilling any of the following criteria was to be excluded from trial enrollment: 1. Participant was 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 until at least 4 weeks after the last vaccination. To be considered of non-childbearing potential, a female must be post-menopausal for at least 1 year, or surgically sterile. 2. Participation at the time of study enrollment or, planned participation during the present trial period in another clinical trial investigating a vaccine, drug, medical device, or medical procedure. 3. Receipt of any vaccine in the 4 weeks (28 days) preceding the first trial vaccination or planned receipt of any vaccine prior to Visit 6. 4. Previous vaccination against rabies (in pre- or post-exposure regimen) with either the trial vaccine or another vaccine. 5. Receipt of immune globulins, blood or blood-derived products in the past 3 months. 6. 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). 7. At high risk for rabies infection during the trial (e.g., veterinarians and staff, animal handlers, rabies researchers, or any others whose activities may bring them into frequent contact with rabies virus or animals who had the rabies virus). 8. Known systemic hypersensitivity to any of the vaccine or human rabies immunoglobulins (HRIG) components, or history of a life-threatening reaction to the vaccines used in the trial or to a vaccine containing any of the same substances. 9. Self-reported thrombocytopenia, contraindicating IM vaccination. 10. Bleeding disorder, or receipt of anticoagulants in the 3 weeks preceding inclusion, contraindicating IM vaccination. 11. Deprived of freedom by an administrative or court order, or in an emergency setting, or hospitalized involuntarily. 12. Current alcohol abuse or drug addiction. 13. Chronic illness that, in the opinion of the investigator, was at a stage where it might interfere with trial conduct or completion (e.g., cardiac disorders, renal disorders, auto immune disorders, diabetes, psychiatric disorders or chronic infection). 14. Moderate or severe acute illness/infection (according to investigator judgment) on the day of vaccination or febrile illness (temperature greater than or equal to \[\>=\] 100.4 Fahrenheit \>=38.0 Celsius). A prospective participant should not be included in the study until the condition had resolved or the febrile event had subsided. 15. 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 (i.e., parent, spouse, natural or adopted child) of the Investigator or employee with direct involvement in the proposed study. 16. History of Guillain-Barré syndrome.

Locations (5)

Investigational Site

Redding, California, United States

Investigational Site

San Diego, California, United States

Investigational Site

South Miami, Florida, United States

Investigational Site

Omaha, Nebraska, United States

Outcomes

Primary Outcomes

Rabies Virus Neutralizing Antibody (RVNA) Geometric Mean Titers (GMTs) Against Rabies Virus at Day 0

RVNA GMT against rabies virus was assessed using the rapid fluorescent focus inhibition test (RFFIT) assay method.

Time frame: Day 0

Rabies Virus Neutralizing Antibody Geometric Mean Titers Against Rabies Virus at Day 14

RVNA GMT against rabies virus was assessed using the RFFIT assay method.

Time frame: Day 14

Rabies Virus Neutralizing Antibody Geometric Mean Titers Against Rabies Virus at Day 28

RVNA GMT against rabies virus was assessed using the RFFIT assay method.

Time frame: Day 28

Rabies Virus Neutralizing Antibody Geometric Mean Titers Against Rabies Virus at Day 42

RVNA GMT against rabies virus was assessed using the RFFIT assay method.

Time frame: Day 42

Rabies Virus Neutralizing Antibody Geometric Mean Titers Against Rabies Virus at Month 7

RVNA GMT against rabies virus was assessed using the RFFIT assay method.

Time frame: Month 7

Percentage of Participants With Rabies Virus Neutralizing Antibody Titer Greater Than or Equal to (>=) 0.2 IU/mL and >=0.5 IU/mL at Day 0

RVNA titer against rabies virus was assessed using the RFFIT assay method. Participants with RVNA titer \>=0.2 IU/mL were considered as seropositive.

Time frame: Day 0

Percentage of Participants With Rabies Virus Neutralizing Antibody Titers >=0.2 IU/mL and >=0.5 IU/mL at Day 14

RVNA titer against rabies virus was assessed using the RFFIT assay method. Participants with RVNA titer \>=0.2 IU/mL were considered as seropositive.

Data from ClinicalTrials.gov

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Modified formulation 2 (Medium) of Purified Vero Rabies Vaccine Serum Free

VRVg 2BIOLOGICAL

Modified formulation 3 (High) of Purified Vero Rabies Vaccine Serum Free

Human Rabies Immunoglobulins (HRIG)BIOLOGICAL

Commercialized formulation of HRIG

Investigational Site

Las Vegas, Nevada, United States

Percentage of Participants With RVNA Titers >=0.2 IU/mL and >=0.5 IU/mL at Day 28

RVNA titer against rabies virus was assessed using the RFFIT assay method. Participants with RVNA titer \>=0.2 IU/mL were considered as seropositive.

Time frame: Day 28

Percentage of Participants With RVNA Titers >=0.2 IU/mL and >=0.5 IU/mL at Day 42

RVNA titer against rabies virus was assessed using the RFFIT assay method. Participants with RVNA titer \>=0.2 IU/mL were considered as seropositive.

Time frame: Day 42

Percentage of Participants With RVNA Titers >=0.2 IU/mL and >=0.5 IU/mL at Month 7

RVNA titer against rabies virus was assessed using the RFFIT assay method. Participants with RVNA titer \>= 0.2 IU/mL were considered as seropositive.

Time frame: Month 7

Geometric Mean Titer Ratio (GMTR) of Rabies Virus Neutralizing Antibody 7 Days Following Vaccination 3 (Day 14/Day 0)

RVNA titer against rabies virus was assessed using the RFFIT assay method. GMTRs were calculated as the ratio of GMTs 7 days post 3rd vaccination (i.e., on Day 14) and pre-vaccination on Day 0.

Time frame: Day 0 (pre-dose) and Day 14 (7 days post-dose 3)

Geometric Mean Titer Ratio of Rabies Virus Neutralizing Antibody 14 Days Following Vaccination 4 (Day 28/Day 0)

RVNA titer against rabies virus was assessed using the RFFIT assay method. GMTRs were calculated as the ratio of GMTs 14 days post 4th vaccination (i.e., on Day 28) and pre-vaccination on Day 0.

Time frame: Day 0 (pre-dose) and Day 28 (14 days post-dose 4)

Geometric Mean Titer Ratio of Rabies Virus Neutralizing Antibody 14 Days Following Vaccination 5 (Day 42/Day 0)

RVNA titer against rabies virus was assessed using the RFFIT assay method. GMTRs were calculated as the ratio of GMTs 14 days post 5th vaccination (i.e., on Day 42) and pre-vaccination on Day 0.

Time frame: Day 0 (Pre-dose) and Day 42 (14 days Post-dose 5)

Geometric Mean Titer Ratio of Rabies Virus Neutralizing Antibody 6 Months Following Last Vaccination (Month 7/Day 0)

RVNA titer against rabies virus was assessed using the RFFIT assay method. GMTRs were calculated as the ratio of GMTs 6 month post last vaccination on Month 7 and pre-vaccination on Day 0.

Time frame: Day 0 (Pre-dose) and Month 7 (6 Months Post Last Vaccination)

Percentage of Participants With Complete Virus Neutralization at Starting Dilution (1/5) of Rapid Fluorescent Focus Inhibition Test Assay at Day 0

Complete virus neutralization was defined as absence of fluorescent cells at the participant/time point level at the starting dilution (1/5) of the RFFIT assay. Percentage of participants with complete virus neutralization were reported.

Time frame: Day 0

Percentage of Participants With Complete Virus Neutralization at Starting Dilution (1/5) of Rapid Fluorescent Focus Inhibition Test Assay at Day 14

Time frame: Day 14

Percentage of Participants With Complete Virus Neutralization at Starting Dilution (1/5) of Rapid Fluorescent Focus Inhibition Test Assay at Day 28

Time frame: Day 28

Percentage of Participants With Complete Virus Neutralization at Starting Dilution (1/5) of Rapid Fluorescent Focus Inhibition Test Assay at Day 42

Time frame: Day 42

Percentage of Participants With Complete Virus Neutralization at Starting Dilution (1/5) of Rapid Fluorescent Focus Inhibition Test Assay at Month 7

Time frame: Month 7

Number of Participants With Immediate Unsolicited Adverse Events

An adverse event was defined as any untoward medical occurrence in a participant who received study drug and does not necessary have to have a causal relationship with treatment. An unsolicited AE was an observed AE that did not fulfill the conditions prelisted in the case report form (CRF) in terms of diagnosis and/or onset post-vaccination. All participants were observed for 30 minutes after any vaccination, and any unsolicited AEs occurred during that time were recorded as immediate unsolicited AEs in the CRF. Immediate AEs considered as related to vaccination were recorded as immediate unsolicited adverse reactions (ARs).

Time frame: Within 30 Minutes After any Vaccination

Number of Participants With at Least One Solicited Injection Site Reactions

A solicited reaction (SR) was an AR observed and reported under conditions (symptoms and onset) prelisted (i.e., solicited) in the CRF and considered as related to vaccination. An AR was all noxious and unintended responses to a medicinal product related to any dose. Solicited injection site reactions included pain, erythema and swelling at and around the injection site.

Time frame: Within 7 Days After any and each vaccination (Vaccination 1, 2, 3, 4 and 5)

Number of Participants With at Least One Solicited Systemic Reactions

A solicited reaction was an AR observed and reported under the conditions (symptom and onset) prelisted (i.e., solicited) in the CRF and considered as related to vaccination. An AR was all noxious and unintended responses to a medicinal product related to any dose. Solicited systemic reactions included fever, headache, malaise and myalgia.

Time frame: Within 7 Days After any and each vaccination (Vaccination 1, 2, 3, 4 and 5)

Number of Participants With at Least One Unsolicited Adverse Events

An AE was defined as any untoward medical occurrence in a participant who received study drug and does not necessary have to have a causal relationship with treatment. An unsolicited AE was an observed AE that did not fulfill the conditions prelisted in the CRF in terms of diagnosis and/or onset post-vaccination.

Time frame: Within 28 Days After any vaccination

Number of Participants With Serious Adverse Events (SAEs)

An AE was defined as any untoward medical occurrence in a participant who received study drug and does not necessary have to have a causal relationship with treatment. An SAE was any untoward medical occurrence that at any dose resulted in death; life-threatening; initial or prolonged inpatient hospitalization; persistent or significant disability/incapacity; congenital anomaly/birth defect or a medically important event.

Time frame: From Day 0 up to Month 7