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Safety and Immunogenicity of BBV121 (Zika)

Primary Purpose

Zika Virus Infection

Status
Completed
Phase
Phase 1
Locations
India
Study Type
Interventional
Intervention
BBV121
Sponsored by
Bharat Biotech International Limited
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Zika Virus Infection

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Normal healthy male and female volunteers aged between 18 and 65 years weighing at least 50kgs of body weight
  2. Ability to comprehend the full nature and purpose of the study, including possible risks and adverse events; ability to co-operate with the Investigator and to comply with the requirements of the entire study
  3. Signed written informed consent prior to inclusion in the study
  4. Seronegative for Zika by ELISA
  5. Dengue sero-negative at baseline by screening laboratory evaluation, confirmed by Dengue IgG by ELISA method for Group 1 participants
  6. Dengue seropositive at baseline by screening laboratory evaluation, confirmed by Dengue IgG by ELISA method for Group 2 participants
  7. Dengue vaccination or suffered from Dengue viral fever for Group 2 volunteers
  8. No history of yellow fever vaccination
  9. No history of vaccination to Japanese encephalitis vaccination
  10. Since active (live) ZIKV infection is known to cause teratogenicity, women of child-bearing potential should agree to use medically effective contraception (oral contraception, barrier methods, spermicide, etc.), preferably double contraception or have a partner who is sterile from enrollment to 3 months following the last injection, or have a male partner who is medically unable to induce pregnancy.
  11. Sexually active men who are considered sexually fertile must agree to use either a barrier method of contraception, preferably double contraception during the study, and agree to continue the use for at least 3 months following the last injection, or have a partner who is permanently sterile or is medically unable to become pregnant.
  12. A negative urine or serum pregnancy test before administration of investigational vaccine on day of screening (Serum Pregnancy Test), and Day 0 and Day 28 (both days Urine Pregnancy Test)
  13. No history of clinically significant immunosuppressive or autoimmune disease.
  14. Laboratory investigations must be within normal limits

    1. Hemoglobin >10gm/dL
    2. WBC (white blood cells) >4000/mm3
    3. Platelets >100,000/mm3
    4. Bilirubin and AST/ ALT <1.5 x ULN (upper limit of normal)
    5. Creatinine <1.5 x ULN for the clinical laboratory
  15. Not currently or within the previous 4 weeks taking immunosuppressive agents (excluding inhaled, topical skin and/or eye drop-containing corticosteroids, low-dose methotrexate, or corticosteroids at a dose less than 20 mg/day).
  16. Patients should be otherwise healthy as determined by physical examination, medical history, and no significant abnormality in any of the clinical parameters including ECG and Chest X-ray.
  17. Willing to allow storage and future use of biological samples for Zika virus related research.

Exclusion Criteria:

  1. Administration of an investigational vaccine or drug either currently or within 30 days of first BBV121 vaccination
  2. Previous receipt of an investigational vaccine or drug for the treatment or prevention of Zika virus
  3. Administration of any vaccine within 4 weeks of first dose
  4. Administration of any monoclonal or polyclonal antibody product within 4 weeks of the first dose of BBV121 vaccination
  5. Administration of any blood product within 3 months of first dose
  6. Pregnancy or breast feeding or plans to become pregnant during the study
  7. Positive serologic test for HIV, hepatitis B surface antigen (HBsAg); or any potentially communicable infectious disease as determined by the Principal Investigator or Medical Monitor
  8. Positive serologic test for hepatitis C (exception: successful treatment with confirmation of sustained virologic response);
  9. Chronic liver disease or cirrhosis
  10. Immunosuppressive illness including hematologic malignancy, history of solid organ or bone marrow transplantation
  11. Current or anticipated concomitant immunosuppressive therapy (excluding inhaled, topical skin and/or eye drop-containing corticosteroids, low-dose methotrexate, or corticosteroids at a dose less than 20 mg/day)
  12. Current or anticipated treatment with TNF-alpha inhibitors such as infliximab, adalimumab, and etanercept
  13. Prior major surgery or any radiation therapy within 4 weeks of enrolment
  14. Any pre-excitation syndromes, e.g., Wolff-Parkinson-White syndrome
  15. Presence of a cardiac pacemaker or automatic implantable cardioverter defibrillator
  16. Metal implants within 20 cm of the planned site(s) of injection
  17. Presence of keloid scar formation or hypertrophic scar at the planned site(s) of injection
  18. Prisoner or participants who are compulsorily detained (involuntary incarceration) for treatment of either a physical or psychiatric illness
  19. Active addictive drug or alcohol use or dependence that, in the opinion of the investigator, would interfere with adherence to study requirements or assessment of immunologic endpoints
  20. Blood donations/ losses within 2 months of screening
  21. Significant orthostatic hypotension (i.e., a drop in systolic blood pressure of 30 mm Hg or more and/or a drop in diastolic blood pressure of 20 mmHg or more on standing)
  22. Prior radiotherapy in 30 days or less
  23. Significant pre-existing co-morbidities i. Cardiovascular

    • Myocardial infarction within the last 6 months
    • Congestive heart failure
    • Unstable angina
    • Active cardiomyopathy
    • Cardiac arrhythmia
    • Uncontrolled hypertension
    • History of familial long QT syndrome or sudden cardiac death ii. Pulmonary disease requiring oxygen iii. Neurologic and psychiatric
    • History of significant neurologic or psychiatric disorder that would preclude study compliance or ability to give informed consent iv. Rheumatic arthralgia
  24. Participants not having adequate hematologic reserve i. Hemoglobin <10gm/dL ii. WBC (white blood cells) <4000/mm3 iii. ANC (absolute neutrophils count) <2000/ mm3 iv. Platelets <100,000/mm3
  25. Inadequate hepatic function at screening as defined by:

    i. Bilirubin >1.5 x ULN (upper limit of normal) ii. AST/ ALT >1.5 x ULN

  26. Inadequate renal function at screening as defined by:

    i. Creatinine >1.5 x ULN for the clinical laboratory

  27. An unusual or abnormal diet, for whatever reason e.g. religious fasting
  28. Any illness or condition that in the opinion of the investigator may affect the safety of the participant or the evaluation of any study endpoint

Sites / Locations

  • Bharat Biotech International Ltd

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Placebo Comparator

Experimental

Experimental

Arm Label

BBV121-2.5 µg

Placebo

BBV121-5 µg

BBV121-10 µg

Arm Description

BBV121: Each 0.5ml vial contain purified10 µg inactivated Zika virus, alum, 2-PE and phosphate buffered saline qs to 0.5mL

Each 0.5ml vial contain purified 2.5 µg, 5 µg or 10 µg inactivated Zika virus, alum, 2-PE and phosphate buffered saline qs to 0.5mL

BBV121: Each 0.5ml vial contain purified inactivated Zika virus, alum, 2-PE and phosphate buffered saline qs to 0.5mL

BBV121: Each 0.5ml vial contain purified inactivated Zika virus, alum, 2-PE and phosphate buffered saline qs to 0.5ml

Outcomes

Primary Outcome Measures

Occurrence of adverse events and Serious Adverse events
safety Incidence of solicited AEs post-vaccination Incidence of unsolicited AEs post-vaccination Incidence of SAE
Occurrence of adverse events and Serious Adverse events
safety
Occurrence of adverse events and Serious Adverse events
safety

Secondary Outcome Measures

Geometric mean titre estimated by 50% plaque reduction neutralization test and four-fold seroconversion
Immunogenicity
Geometric mean titre estimated by 50% plaque reduction neutralization test and four-fold seroconversion
Immunogenicity
Geometric mean titre estimated by 50% plaque reduction neutralization test and four-fold seroconversion
Immunogenicity
Geometric mean titre estimated by 50% plaque reduction neutralization test
Immunogenicity

Full Information

First Posted
July 17, 2017
Last Updated
October 20, 2020
Sponsor
Bharat Biotech International Limited
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1. Study Identification

Unique Protocol Identification Number
NCT04478656
Brief Title
Safety and Immunogenicity of BBV121
Acronym
Zika
Official Title
Phase 1, Multicenter, Double-Blind, Placebo-Controlled, Randomized Clinical Trial to Evaluate 2 Doses of 3 Sequentially Escalating Cohort of BBV121 in Healthy Adult Dengue Sero-Negative and Dengue Sero-Positive Volunteers
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Completed
Study Start Date
June 3, 2017 (Actual)
Primary Completion Date
November 15, 2017 (Actual)
Study Completion Date
November 15, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Bharat Biotech International Limited

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
To evaluate the safety, tolerability, and immunogenicity of two-doses of three-sequentially escalating cohort (2.5 µg, 5 µg and 10 µg) of BBV121 (purified inactivated adsorbed Zika virus vaccine) compared with Placebo (Alum). The investigational product is administered intramuscularly on Day 0 and 28 with safety and immunogenicity testing on Day 0, 28 and 56, and Month 6, 9 and 12
Detailed Description
A phase 1, multicenter, double-blind, placebo-controlled, randomised (intra group) clinical trial to evaluate the safety, tolerability and immunogenicity of two-doses of three-sequentially escalating cohort (2.5 µg, 5 µg and 10 µg) of BBV121 (inactivated adsorbed Zika Virus Vaccine) compared with Placebo (Alum) administered intramuscularly on Day 0 and 28 in healthy adult Dengue Sero-Negative (Group 1) and Dengue Sero-Positive (Group 2) male and female volunteers. Participants will be assigned to sequential escalating dose level groups to receive vaccinations at 2.5 µg, 5 µg, or 10 µg or Placebo on Day 0 and 28 with follow-up for 12 months from initial administration of the investigational product. Immunogenicity testing on Day 0, 28 and 56, and post-study at the end of Month 6, 9 and 12 after the initial administration of the investigational product. Safety tests (laboratory and clinical investigations) will be done during Screening, Day 0, 28, 56, and post-study at Month 6, 9 and 12 months after the initial administration of the investigational product.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Zika Virus Infection

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Model Description
Participants will be assigned to sequential escalating dose level groups to receive vaccinations at 2.5 µg, 5 µg, or 10 µg or Placebo on Day 0 and 28 with follow-up for 12 months from initial administration of the investigational product.
Masking
ParticipantInvestigator
Masking Description
Blinded vial
Allocation
Randomized
Enrollment
48 (Actual)

8. Arms, Groups, and Interventions

Arm Title
BBV121-2.5 µg
Arm Type
Experimental
Arm Description
BBV121: Each 0.5ml vial contain purified10 µg inactivated Zika virus, alum, 2-PE and phosphate buffered saline qs to 0.5mL
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Each 0.5ml vial contain purified 2.5 µg, 5 µg or 10 µg inactivated Zika virus, alum, 2-PE and phosphate buffered saline qs to 0.5mL
Arm Title
BBV121-5 µg
Arm Type
Experimental
Arm Description
BBV121: Each 0.5ml vial contain purified inactivated Zika virus, alum, 2-PE and phosphate buffered saline qs to 0.5mL
Arm Title
BBV121-10 µg
Arm Type
Experimental
Arm Description
BBV121: Each 0.5ml vial contain purified inactivated Zika virus, alum, 2-PE and phosphate buffered saline qs to 0.5ml
Intervention Type
Biological
Intervention Name(s)
BBV121
Other Intervention Name(s)
Placebo
Intervention Description
BBV121 or Placebo are administered intramuscularly in deltoid region on Day 0 and 28
Primary Outcome Measure Information:
Title
Occurrence of adverse events and Serious Adverse events
Description
safety Incidence of solicited AEs post-vaccination Incidence of unsolicited AEs post-vaccination Incidence of SAE
Time Frame
Within 2 hrs
Title
Occurrence of adverse events and Serious Adverse events
Description
safety
Time Frame
7 Days
Title
Occurrence of adverse events and Serious Adverse events
Description
safety
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Geometric mean titre estimated by 50% plaque reduction neutralization test and four-fold seroconversion
Description
Immunogenicity
Time Frame
Day 0
Title
Geometric mean titre estimated by 50% plaque reduction neutralization test and four-fold seroconversion
Description
Immunogenicity
Time Frame
Day 28
Title
Geometric mean titre estimated by 50% plaque reduction neutralization test and four-fold seroconversion
Description
Immunogenicity
Time Frame
Day 56
Title
Geometric mean titre estimated by 50% plaque reduction neutralization test
Description
Immunogenicity
Time Frame
Day 365

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Normal healthy male and female volunteers aged between 18 and 65 years weighing at least 50kgs of body weight Ability to comprehend the full nature and purpose of the study, including possible risks and adverse events; ability to co-operate with the Investigator and to comply with the requirements of the entire study Signed written informed consent prior to inclusion in the study Seronegative for Zika by ELISA Dengue sero-negative at baseline by screening laboratory evaluation, confirmed by Dengue IgG by ELISA method for Group 1 participants Dengue seropositive at baseline by screening laboratory evaluation, confirmed by Dengue IgG by ELISA method for Group 2 participants Dengue vaccination or suffered from Dengue viral fever for Group 2 volunteers No history of yellow fever vaccination No history of vaccination to Japanese encephalitis vaccination Since active (live) ZIKV infection is known to cause teratogenicity, women of child-bearing potential should agree to use medically effective contraception (oral contraception, barrier methods, spermicide, etc.), preferably double contraception or have a partner who is sterile from enrollment to 3 months following the last injection, or have a male partner who is medically unable to induce pregnancy. Sexually active men who are considered sexually fertile must agree to use either a barrier method of contraception, preferably double contraception during the study, and agree to continue the use for at least 3 months following the last injection, or have a partner who is permanently sterile or is medically unable to become pregnant. A negative urine or serum pregnancy test before administration of investigational vaccine on day of screening (Serum Pregnancy Test), and Day 0 and Day 28 (both days Urine Pregnancy Test) No history of clinically significant immunosuppressive or autoimmune disease. Laboratory investigations must be within normal limits Hemoglobin >10gm/dL WBC (white blood cells) >4000/mm3 Platelets >100,000/mm3 Bilirubin and AST/ ALT <1.5 x ULN (upper limit of normal) Creatinine <1.5 x ULN for the clinical laboratory Not currently or within the previous 4 weeks taking immunosuppressive agents (excluding inhaled, topical skin and/or eye drop-containing corticosteroids, low-dose methotrexate, or corticosteroids at a dose less than 20 mg/day). Patients should be otherwise healthy as determined by physical examination, medical history, and no significant abnormality in any of the clinical parameters including ECG and Chest X-ray. Willing to allow storage and future use of biological samples for Zika virus related research. Exclusion Criteria: Administration of an investigational vaccine or drug either currently or within 30 days of first BBV121 vaccination Previous receipt of an investigational vaccine or drug for the treatment or prevention of Zika virus Administration of any vaccine within 4 weeks of first dose Administration of any monoclonal or polyclonal antibody product within 4 weeks of the first dose of BBV121 vaccination Administration of any blood product within 3 months of first dose Pregnancy or breast feeding or plans to become pregnant during the study Positive serologic test for HIV, hepatitis B surface antigen (HBsAg); or any potentially communicable infectious disease as determined by the Principal Investigator or Medical Monitor Positive serologic test for hepatitis C (exception: successful treatment with confirmation of sustained virologic response); Chronic liver disease or cirrhosis Immunosuppressive illness including hematologic malignancy, history of solid organ or bone marrow transplantation Current or anticipated concomitant immunosuppressive therapy (excluding inhaled, topical skin and/or eye drop-containing corticosteroids, low-dose methotrexate, or corticosteroids at a dose less than 20 mg/day) Current or anticipated treatment with TNF-alpha inhibitors such as infliximab, adalimumab, and etanercept Prior major surgery or any radiation therapy within 4 weeks of enrolment Any pre-excitation syndromes, e.g., Wolff-Parkinson-White syndrome Presence of a cardiac pacemaker or automatic implantable cardioverter defibrillator Metal implants within 20 cm of the planned site(s) of injection Presence of keloid scar formation or hypertrophic scar at the planned site(s) of injection Prisoner or participants who are compulsorily detained (involuntary incarceration) for treatment of either a physical or psychiatric illness Active addictive drug or alcohol use or dependence that, in the opinion of the investigator, would interfere with adherence to study requirements or assessment of immunologic endpoints Blood donations/ losses within 2 months of screening Significant orthostatic hypotension (i.e., a drop in systolic blood pressure of 30 mm Hg or more and/or a drop in diastolic blood pressure of 20 mmHg or more on standing) Prior radiotherapy in 30 days or less Significant pre-existing co-morbidities i. Cardiovascular Myocardial infarction within the last 6 months Congestive heart failure Unstable angina Active cardiomyopathy Cardiac arrhythmia Uncontrolled hypertension History of familial long QT syndrome or sudden cardiac death ii. Pulmonary disease requiring oxygen iii. Neurologic and psychiatric History of significant neurologic or psychiatric disorder that would preclude study compliance or ability to give informed consent iv. Rheumatic arthralgia Participants not having adequate hematologic reserve i. Hemoglobin <10gm/dL ii. WBC (white blood cells) <4000/mm3 iii. ANC (absolute neutrophils count) <2000/ mm3 iv. Platelets <100,000/mm3 Inadequate hepatic function at screening as defined by: i. Bilirubin >1.5 x ULN (upper limit of normal) ii. AST/ ALT >1.5 x ULN Inadequate renal function at screening as defined by: i. Creatinine >1.5 x ULN for the clinical laboratory An unusual or abnormal diet, for whatever reason e.g. religious fasting Any illness or condition that in the opinion of the investigator may affect the safety of the participant or the evaluation of any study endpoint
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sudhakar Bangera
Organizational Affiliation
Bharat Biotech International Limited
Official's Role
Study Chair
Facility Information:
Facility Name
Bharat Biotech International Ltd
City
Hyderabad
State/Province
Telangana
ZIP/Postal Code
500078
Country
India

12. IPD Sharing Statement

Plan to Share IPD
No

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Safety and Immunogenicity of BBV121

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