Clinical Trial to Evaluate the Immunogenicity of Chikungunya Vaccine

• ClinicalTrials.gov Identifier: NCT04603131
• Recruitment Status: Completed
• First Posted: October 26, 2020
• Last Update Posted: October 28, 2020
• Sponsor: Bharat Biotech International Limited
• Information provided by (Responsible Party): Bharat Biotech International Limited

Study Description

Brief Summary:

Chikungunya vaccine is an inactivated virus vaccine. There will be three study arms and subjects will be vaccinated in a dose escalation manner.In each arm, vaccine will be administered on Day 1, Day 29, and Day 57. Vaccine will be administered through intramuscular route.

Condition or disease	Intervention/treatment	Phase
Chikungunya	Biological: Inactivated Chikungunya virus vaccine 20 mcg; Biological: Inactivated Chikungunya virus vaccine 30 mcg; Biological: Inactivated Chikungunya virus vaccine 10 mcg; Biological: Placebo	Phase 1

Detailed Description:

This is an open label phase I study for assessing the safety, tolerance and immunogenicity of 3 escalated doses of the test vaccine, BBV87. The study design has four treatment groups - 3 test groups and a control placebo group with 15 subjects in each group. However, the groups will be divided into three study arms: each arm will have 15 subjects of the test vaccine group and 5 subjects of the placebo group. The randomization will be done in a way that allots 5 subjects of the placebo group to each test dose group. All subjects will be screened (via medical history, physical examination and laboratory investigations) to establish the eligibility criteria. This includes negative antibodies, CHIKV IgG, by ELISA method. The test vaccine and placebo will be administered as 3 doses at 28 days interval on day 1±2, 29±2, and 57±2. Vaccine administration will be performed as an in-patient procedure. Subjects will be admitted in CPU 24 hrs prior to vaccine administration, and will be shifted to MICU for vaccination and observed for 48 hrs; and will be discharged upon completion of all clinical monitoring procedures. Laboratory and biochemical tests will be performed as part of clinical monitoring before discharge, and 24 hrs after vaccine administration. Following vaccination, all participants will be monitored throughout the study period for adverse events with daily telephone contacts (for 7 days after each vaccine, and then weekly), interim clinic visits, subject diary cards, and haematological & biochemical laboratory tests.

Study Design

• Study Type: Interventional (Clinical Trial)
• Actual Enrollment: 60 participants
• Allocation: Randomized
• Intervention Model: Sequential Assignment
• Intervention Model Description: Chikungunya vaccine is an inactivated virus vaccine. There will be three study arms and subjects will be vaccinated in a dose escalation manner.In each arm, vaccine will be administered on day1, day29, day57. Vaccine will be administered through intramuscular route.
• Masking: None (Open Label)
• Primary Purpose: Prevention
• Official Title: Phase-I Open Label, Dose-escalation Clinical Trial to Evaluate the Safety, Tolerability and Immunogenicity of Chikungunya Vaccine in Healthy Adults of 18 to 50 Years Age
• Actual Study Start Date: April 17, 2017
• Actual Primary Completion Date: January 30, 2018
• Actual Study Completion Date: July 30, 2018

Arms and Interventions

Arm	Intervention/treatment
Experimental: BBV87 - 10 mcg; Inactivated Chikungunya virus vaccine (BBV87) in three dose strengths (10, 20 and 30 mcg) administered intramuscularly on Day 0, 29 and 57	Biological: Inactivated Chikungunya virus vaccine 10 mcg; 3 doses of Inactivated Chikungunya virus vaccine (BBV87) administered intramuscularly on Day 0, 29 and 57
Placebo Comparator: Placebo; Placebo administered intramuscularly on Day 0, 29 and 57	Biological: Placebo; 3 doses of Placebo administered intramuscularly on Day 0, 29 and 57
Experimental: BBV87 -30 mcg; Inactivated Chikungunya virus vaccine (BBV87) in three dose strengths administered intramuscularly on Day 0, 29 and 57	Biological: Inactivated Chikungunya virus vaccine 20 mcg; 3 doses of Inactivated Chikungunya virus vaccine (BBV87) administered intramuscularly on Day 0, 29 and 57
Experimental: BBV87 -20 mcg; Inactivated Chikungunya virus vaccine (BBV87) in three dose strengths administered intramuscularly on Day 0, 29 and 57	Biological: Inactivated Chikungunya virus vaccine 30 mcg; 3 doses of Inactivated Chikungunya virus vaccine (BBV87) administered intramuscularly on Day 0, 29 and 57

Outcome Measures

Primary Outcome Measures :

1. Occurrence of adverse events and Serious Adverse events post each dose [ Time Frame: Within 24 hrs ]
   safety
2. Occurrence of adverse events and Serious Adverse events post each dose [ Time Frame: 7 Days, ]
   safety
3. Occurrence of adverse events and Serious Adverse event 28 days after the last dose of vaccine [ Time Frame: 9 months ]
   safety

Secondary Outcome Measures :

1. Immunogenicity in terms of GMT estimated by 50 percent plaque reduction neutralization test [ Time Frame: day 28 ]
   Immunogenicity
2. Immunogenicity in terms of GMT estimated by 50 percent plaque reduction neutralization test [ Time Frame: day 56 ]
   Immunogenicity
3. Immunogenicity in terms of GMT estimated by 50 percent plaque reduction neutralization test [ Time Frame: day 84 ]
   Immunogenicity
4. Proportion of subjects with four fold seroconversion [ Time Frame: day 28 ]
   Immunogenicity
5. Proportion of subjects with four fold seroconversion [ Time Frame: day 56 ]
   Immunogenicity
6. Proportion of subjects with four fold seroconversion [ Time Frame: day 84 ]
   Immunogenicity

Eligibility Criteria

• Ages Eligible for Study: 18 Years to 50 Years (Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Criteria

Inclusion Criteria:

• ≥18 and ≤50 yrs inclusive on the day of screening
• Able and willing to complete informed consent process with understanding of the purpose and procedures of the study
• Medical history and physical examination without clinically significant findings at the time of screening
• Haematological and biochemical values either within institutional normal range and accompanied by physician approval
• Agree to keep a daily record of symptoms for the duration of the study
• Available for clinical follow-up throughout the study period via telephone contact as well as clinic visits

Female specific criteria:

• If female of child bearing potential- have a negative urine pregnancy test result within 24 hrs of the scheduled first vaccination

Exclusion Criteria:

Female specific criteria:

• Woman who is breast feeding or planning to become pregnant during the study period.

General Criteria:

• History of suspected or confirmed Chikungunya fever

(Case definition for Suspected Chikungunya: A subject meeting both the clinical and epidemiological criteria.

• Clinical criteria: acute onset of fever >38.5°C and severe arthralgia/arthritis not explained by other medical conditions.
• Epidemiological criteria: residing or having visited epidemic areas, having reported transmission within 15 days prior to the onset of symptoms.

Case definition for Confirmed Chikungunya:

A subject meeting the laboratory criteria of positive ELISA test for CHIKV IgG.)

• Clinically significant abnormal clinical laboratory values including blood pressure(>140 mmHg systolic and >90 mmHg diastolic) when 3 measurements are taken 30 min apart , in seating position and at rest
• Body mass index (BMI) ≥ 25 [BMI will be calculated as weight in Kilograms/(height in metres)2]
• Test positive for HIV or Hepatitis B infection
• History of cardiovascular disease
• History of immune deficiency or autoimmune disease
• Have active or history of arthritis (joint swelling, pain, tenderness, warmth or erythema) within the last 6 months from date of screening
• Have an active or history of malignant conditions including haematological malignancy
• Have a history of degenerative neurological disease (e.g. GuillainBarre Syndrome, multiple sclerosis)
• Have received any vaccination within 4 weeks prior to the vaccination in this study
• Have received blood transfusion or immunoglobulin within 30 days prior to vaccination in this study
• Have a history of serious reactions to any vaccines that preclude receipt of study vaccinations as determined by the investigator
• Have asthma that is unstable or required emergent care, urgent care, hospitalization or intubation during the past two years or that is expected to require the use of oral or intravenous corticosteroids
• Have diabetes mellitus (type I or II), with the exception of history of gestational diabetes
• Have received any investigational drug in 6 weeks prior to screening
• Is currently participating in any form of clinical trial that involves intervention.
• Is likely to participate in any other clinical trial during the study period.

Contacts and Locations

Locations

India

King George Hospital

Visakhapatnam, Andhra Pradesh, India

Medanta - The Medicity

Gurgaon, Haryana, India

KEM Hospital

Mumbai, Maharastra, India

Panchsheel Hospital

Delhi, India

Sponsors and Collaborators

Bharat Biotech International Limited

Investigators

• Study Director: Krishna Mohan, PHD; Bharat Biotech International Limited

More Information

• Responsible Party: Bharat Biotech International Limited
• ClinicalTrials.gov Identifier: NCT04603131
• Other Study ID Numbers: BBIL/CHIKV/I/2014
• First Posted: October 26, 2020
• Last Update Posted: October 28, 2020
• Last Verified: October 2020

Individual Participant Data (IPD) Sharing Statement:

• Plan to Share IPD: No

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:

Chikungunya Fever; Alphavirus Infections; Arbovirus Infections; Vector Borne Diseases; Infections; Virus Diseases; Togaviridae Infections; RNA Virus Infections; Vaccines; Immunologic Factors; Physiological Effects of Drugs