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Determining Safety and Efficacy of Japanese Encephalitis Vaccine When Given With Measles Vaccine

Assessment of the Non-Inferiority of the Concurrent Administration of Japanese Encephalitis Live Attenuated SA 14-14-2 Vaccine and Measles Vaccine Given Alone

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00249769
Enrollment
600
Registered
2005-11-07
Start date
2005-11-21
Completion date
2006-05-30
Last updated
2020-03-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Encephalitis, Japanese B

Keywords

Japanese Encephalitis, Japanese B Encephalitis, Japanese B Viral Encephalitis, Viral Encephalitis, Japanese B

Brief summary

This study will determine whether it is safe and effective to administer Japanese encephalitis (JE) live attenuated SA 14-14-2 vaccine at the same time as measles vaccine. If it is found to be safe, it will pave the way for use in routine vaccination programs. The hypothesis is that children who receive JE live attenuated SA 14-14-2 vaccine and measles vaccine at the same time are protected against these diseases at the same level as those who receive the vaccines at different intervals.

Detailed description

Japanese encephalitis is the leading cause of viral neurological disease and disability in Asia. The severity of sequelae, together with the volume of cases, make JE the most important cause of viral encephalitis in the world. Approximately 3 billion people-including 700 million children-live in Asian areas at risk for JE. JE most commonly infects children between the ages of 1 and 15 years, and can also infect adults in areas where the virus is newly introduced. More than 50,000 cases are reported annually and cause an estimated 10,000 to 15,000 deaths. This figure is believed to represent only a small proportion of the disease burden that actually exists. An effective vaccine has existed since 1941, but has not reached the poorest countries in Asia. During the 60 years that the vaccine has been available, JE has infected an estimated 10.5 million children, resulting in more than 3 million deaths and more than 4 million children living with long-term disabilities. Control of this disease has been limited due to poor disease surveillance, a limited and unstable vaccine supply, lack of guidance and programmatic support for immunization, and limited advocacy. A successful vaccine should be safe, efficacious, affordable, administered in a single dose, and easily incorporated into the routine Expanded Programmes on Immunization (EPI) programs. This study will help ensure the safety of SA 14-14-2 simultaneously administered with measles vaccine, paving the way for its use in routine EPI programs. If this candidate becomes widely available, it will drastically increase the feasibility of routine JE immunization in Asia, reducing the devastating death and disability caused by this disease. In addition to impacting low-income countries, the vaccine will allow countries that purchase vaccine-such as Thailand, Vietnam, Sri Lanka, and India-to recover health care dollars, improve their present programs, and address other unmet health care needs.

Interventions

BIOLOGICALLive Japanese encephalitis vaccine SA 14-14-2 (LJEV)

Live Japanese encephalitis vaccine SA 14-14-2 (LJEV) is lyophilized powder that looks like a milky-white crisp cake. After reconstitution, it turns into a transparent orange red liquid. Its container is a vial. It is stored and transported between 2°C to 8°C and protected from light. Each single human dose is 0.5 ml containing not less than 5.4 log particle flux unit (PFU) of live Japanese Encephalitis (JE) virus. The 0.5ml injection is delivered subcutaneously via auto-disable syringe. Lot number 200411129-3 manufactured by Chengdu Institute of Biological Products (CDIBP), Chengdu, China.

The Serum Institute of India (SII) measles vaccine provided routinely in the Expanded Program on Immunization (EPI) of the Philippines was the measles vaccine provided to the study participants. The vaccine met the requirements of the World Health Organization (WHO). SII measles vaccine contained live attenuated (freeze-dried) Edmonston-Zagreb strain measles virus propagated on human diploid cells (HDC). Each single human dose when reconstituted in a volume of 0.5 ml contains no less than 1000 Cell culture infectious dose 50% (CCID50) of live virus particles. SII measles vaccine is presented as a yellowish-white dry cake. The vaccine should be reconstituted with the diluent supplied (sterile water for injection). A sterile disposable syringe and needle are supplied separately. The 0.5ml injection is delivered subcutaneously via auto-disable syringe. Lot number 2979.

Sponsors

Research Institute for Tropical Medicine, Manila, Philippines
CollaboratorUNKNOWN
Quintiles, Inc.
CollaboratorINDUSTRY
Mahidol University
CollaboratorOTHER
PATH
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
8 Months to 11 Months
Healthy volunteers
Yes

Inclusion criteria

* Participant is healthy, aged between 8 months (± 2 weeks) at inclusion visit * Subject is a full-term infant * Subject's parents or legal guardian willing to provide signed informed consent. * Children have completed 3 doses each of diphtheria, tetanus, pertussis (DTP) and oral polio vaccine (OPV).

Exclusion criteria

* History of documented HIV. * Known or suspected impairment of immunologic function. * History of serious chronic disease * Underlying medical condition such as inborn errors of metabolism, failure to thrive, bronchopulmonary dysplasia, or any major congenital abnormalities requiring surgery or chronic treatment. * Acute medical illness with or without fever within the last 72 hours or an axillary temperature ≥ 37.5°C at the time of inclusion. * History of documented suspected encephalitis, encephalopathy, or meningitis * History of measles * History of thrombocytopenic purpura. * Received any JE or measles vaccine prior to enrollment. * Received any vaccine, other than the study vaccines, within 2 weeks prior to or scheduled to receive a non-study vaccination during the conduct of this trial. * Hypotonic - hyporesponsiveness, after the preceding vaccination. * History of seizures, including history of febrile seizures, or any other neurologic disorder. * Prior or anticipated receipt of immune globulin or other blood products, or injected or oral corticosteroids or other immune modulator therapy except routine vaccines within 6 weeks of administration of the study vaccines. Individuals on a tapering dose schedule of oral steroids lasting \<7 days may be included in the trial as long as they have not received more than one course within the last 2 weeks prior to enrollment. * Suspected or known hypersensitivity to any of the investigational or marketed vaccine components. * Serious adverse event related to the vaccine (i.e., possible, probably, definite) * Persistent inconsolable crying (\>3 hours) observed after a previous dose. * Unable to attend the scheduled visits or comply with the study procedures. * Enrolled in another clinical trial involving any therapy. * Any condition that in the opinion of the investigator, would pose a health risk to the participant, or interfere with the evaluation of the study objectives.

Design outcomes

Primary

MeasureTime frameDescription
Percentage of Participants With Seroprotection for Measles 4 Weeks After VaccinationDay 0 (before vaccination) and Day 28 (4 weeks after measles vaccination)Seroprotection after measles vaccination was defined as a measles antibody titer ≥ 120 mIU/mL. Measles immunoglobulin G (IgG) antibody was determined using the Enzygnost® Anti-Measles Virus/IgG enzyme-linked immunosorbent assay(ELISA) assay from Siemens, Marburg, Germany.

Secondary

MeasureTime frameDescription
Geometric Mean Concentration (GMC) of Measles Antibodies After VaccinationDay 0 (before vaccination) and Day 28 (4 weeks after measles vaccination)Measured using the Enzygnost® Anti-Measles Virus/IgG ELISA assay from Siemens, Marburg, Germany.
Geometric Mean Titer (GMT) of Japanese Encephalitis Antibodies After VaccinationDay 0 (before vaccination) and Day 28 (4 weeks after LJEV vaccination)Assayed by plaque reduction neutralization test (PRNT).
Percentage of Participants With Seroprotection for Japanese Encephalitis 4 Weeks After VaccinationDay 0 (before vaccination) and Day 28 (4 weeks after LJEV vaccination)Seroprotection after LJEV was defined as at least 1:10 dilution as recommended by the World Health Organization (WHO). JE antibody titers were determined by a plaque reduction neutralization test (PRNT).
Number of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineUp to 7 days after measles vaccinationLocal reactions included erythema, pain, swelling, and induration. Systemic reactions included loss of appetite, crying, diarrhea, drowsiness, insomnia, irritability, and vomiting. The parents of the participants recorded all local reactions and systemic events on an individual safety diary form.
Number of Participants Experiencing Unsolicited Adverse Events (AE)Up to 7 days post-vaccination
Number of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Up to 7 days after LJEV administrationLocal reactions included erythema, pain, swelling, or induration. Systemic reactions included loss of appetite, crying, diarrhea, drowsiness, insomnia, irritability, vomiting, or fever. The parents of the participants recorded all local reactions and systemic events on an individual safety diary form.

Countries

Philippines

Participant flow

Participants by arm

ArmCount
LJEV Then MV
Received one dose of Live Japanese encephalitis vaccine SA 14-14-2 (LJEV) at 8 months of age, and one dose of measles vaccine (MV) one month later.
100
LJEV and MV
Received one dose of Live Japanese encephalitis vaccine SA 14-14-2 (LJEV) concurrently with one dose of measles vaccine (MV) at 9 months of age.
236
MV Then LJEV
Received one dose of measles vaccine (MV) at 9 months of age, followed by one dose of Live Japanese encephalitis vaccine SA 14-14-2 (LJEV) one month later.
235
Total571

Withdrawals & dropouts

PeriodReasonFG000FG001FG002
Overall StudyAdverse Event001
Overall StudyLost to Follow-up003
Overall StudyMigration from Study Area1314
Overall StudyMiscellaneous022
Overall StudyPhysician Decision002
Overall StudyWithdrawal by Subject1106

Baseline characteristics

CharacteristicLJEV Then MVLJEV and MVMV Then LJEVTotal
Age, Continuous7.9 months
STANDARD_DEVIATION 0.3
8.9 months
STANDARD_DEVIATION 0.3
8.9 months
STANDARD_DEVIATION 0.3
8.7 months
STANDARD_DEVIATION 0.5
Height66.3 centimeters
STANDARD_DEVIATION 2.6
67.6 centimeters
STANDARD_DEVIATION 2.7
67.7 centimeters
STANDARD_DEVIATION 2.6
67.4 centimeters
STANDARD_DEVIATION 2.7
Sex: Female, Male
Female
48 Participants108 Participants128 Participants284 Participants
Sex: Female, Male
Male
52 Participants128 Participants107 Participants287 Participants
Weight7.9 kilograms
STANDARD_DEVIATION 1
8.0 kilograms
STANDARD_DEVIATION 1
8.1 kilograms
STANDARD_DEVIATION 1
8.0 kilograms
STANDARD_DEVIATION 1

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
deaths
Total, all-cause mortality
0 / 1000 / 2360 / 235
other
Total, other adverse events
34 / 10043 / 23678 / 235
serious
Total, serious adverse events
5 / 1000 / 2367 / 235

Outcome results

Primary

Percentage of Participants With Seroprotection for Measles 4 Weeks After Vaccination

Seroprotection after measles vaccination was defined as a measles antibody titer ≥ 120 mIU/mL. Measles immunoglobulin G (IgG) antibody was determined using the Enzygnost® Anti-Measles Virus/IgG enzyme-linked immunosorbent assay(ELISA) assay from Siemens, Marburg, Germany.

Time frame: Day 0 (before vaccination) and Day 28 (4 weeks after measles vaccination)

Population: The per-protocol population includes randomized participants who received at least one vaccine dose excluding participants who did not meet the inclusion/exclusion criteria or were found non-compliant to the immunization or blood sampling schedule. The analysis includes participants with valid serology results for measles antibody during retesting.

ArmMeasureGroupValue (NUMBER)
LJEV Then MVPercentage of Participants With Seroprotection for Measles 4 Weeks After VaccinationDay 01.1 percentage of participants
LJEV Then MVPercentage of Participants With Seroprotection for Measles 4 Weeks After VaccinationDay 2888.6 percentage of participants
LJEV and MVPercentage of Participants With Seroprotection for Measles 4 Weeks After VaccinationDay 00.0 percentage of participants
LJEV and MVPercentage of Participants With Seroprotection for Measles 4 Weeks After VaccinationDay 2891.8 percentage of participants
MV Then LJEVPercentage of Participants With Seroprotection for Measles 4 Weeks After VaccinationDay 2886.5 percentage of participants
MV Then LJEVPercentage of Participants With Seroprotection for Measles 4 Weeks After VaccinationDay 00.0 percentage of participants
Secondary

Geometric Mean Concentration (GMC) of Measles Antibodies After Vaccination

Measured using the Enzygnost® Anti-Measles Virus/IgG ELISA assay from Siemens, Marburg, Germany.

Time frame: Day 0 (before vaccination) and Day 28 (4 weeks after measles vaccination)

Population: Per-protocol population; the analysis includes participants with valid serology results for measles antibody during retesting.

ArmMeasureGroupValue (GEOMETRIC_MEAN)
LJEV Then MVGeometric Mean Concentration (GMC) of Measles Antibodies After VaccinationDay 012.8 mIU/mL
LJEV Then MVGeometric Mean Concentration (GMC) of Measles Antibodies After VaccinationDay 28318.9 mIU/mL
LJEV and MVGeometric Mean Concentration (GMC) of Measles Antibodies After VaccinationDay 07.4 mIU/mL
LJEV and MVGeometric Mean Concentration (GMC) of Measles Antibodies After VaccinationDay 28301.9 mIU/mL
MV Then LJEVGeometric Mean Concentration (GMC) of Measles Antibodies After VaccinationDay 07.0 mIU/mL
MV Then LJEVGeometric Mean Concentration (GMC) of Measles Antibodies After VaccinationDay 28262.5 mIU/mL
Secondary

Geometric Mean Titer (GMT) of Japanese Encephalitis Antibodies After Vaccination

Assayed by plaque reduction neutralization test (PRNT).

Time frame: Day 0 (before vaccination) and Day 28 (4 weeks after LJEV vaccination)

Population: Per-protocol population

ArmMeasureGroupValue (GEOMETRIC_MEAN)
LJEV Then MVGeometric Mean Titer (GMT) of Japanese Encephalitis Antibodies After VaccinationDay 05.7 titer
LJEV Then MVGeometric Mean Titer (GMT) of Japanese Encephalitis Antibodies After VaccinationDay 28202.8 titer
LJEV and MVGeometric Mean Titer (GMT) of Japanese Encephalitis Antibodies After VaccinationDay 05.7 titer
LJEV and MVGeometric Mean Titer (GMT) of Japanese Encephalitis Antibodies After VaccinationDay 28155.0 titer
MV Then LJEVGeometric Mean Titer (GMT) of Japanese Encephalitis Antibodies After VaccinationDay 05.9 titer
MV Then LJEVGeometric Mean Titer (GMT) of Japanese Encephalitis Antibodies After VaccinationDay 28139.4 titer
Secondary

Number of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)

Local reactions included erythema, pain, swelling, or induration. Systemic reactions included loss of appetite, crying, diarrhea, drowsiness, insomnia, irritability, vomiting, or fever. The parents of the participants recorded all local reactions and systemic events on an individual safety diary form.

Time frame: Up to 7 days after LJEV administration

Population: Participants who received LJEV

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Local reactions: any27 Participants
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Local reactions: mild19 Participants
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Local reactions: moderate8 Participants
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Local reactions: severe0 Participants
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Systemic reactions: any58 Participants
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Systemic reaction: mild34 Participants
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Systemic reaction: moderate22 Participants
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Systemic reaction: severe2 Participants
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Fever: any24 Participants
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Fever: 37.5-38.6°C18 Participants
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Fever: 38.7-39.9°C6 Participants
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Fever: ≥ 40°C0 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Fever: ≥ 40°C0 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Local reactions: any53 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Systemic reaction: moderate37 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Fever: any52 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Local reactions: mild48 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Systemic reaction: mild53 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Fever: 38.7-39.9°C14 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Local reactions: moderate5 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Systemic reaction: severe7 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Systemic reactions: any97 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Local reactions: severe0 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Fever: 37.5-38.6°C38 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Local reactions: severe0 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Systemic reactions: any88 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Fever: 37.5-38.6°C47 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Systemic reaction: mild56 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Systemic reaction: moderate30 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Systemic reaction: severe2 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Fever: 38.7-39.9°C10 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Local reactions: any27 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Local reactions: mild22 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Fever: any57 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Local reactions: moderate5 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Live Attenuated Japanese Encephalitis Vaccine (LJEV)Fever: ≥ 40°C0 Participants
Secondary

Number of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles Vaccine

Local reactions included erythema, pain, swelling, and induration. Systemic reactions included loss of appetite, crying, diarrhea, drowsiness, insomnia, irritability, and vomiting. The parents of the participants recorded all local reactions and systemic events on an individual safety diary form.

Time frame: Up to 7 days after measles vaccination

Population: Participants who received measles vaccine

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineLocal reactions: any19 Participants
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineLocal reactions: mild15 Participants
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineLocal reactions: moderate4 Participants
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineLocal reactions: severe0 Participants
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineSystemic reactions: any49 Participants
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineSystemic reaction: mild31 Participants
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineSystemic reaction: moderate13 Participants
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineSystemic reaction: severe5 Participants
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineFever: any31 Participants
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineFever: 37.5-38.6°C21 Participants
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineFever: 38.7-39.9°C10 Participants
LJEV Then MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineFever: ≥ 40°C0 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineFever: ≥ 40°C0 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineLocal reactions: any44 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineSystemic reaction: moderate37 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineFever: any52 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineLocal reactions: mild42 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineSystemic reaction: mild53 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineFever: 38.7-39.9°C14 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineLocal reactions: moderate2 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineSystemic reaction: severe7 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineSystemic reactions: any97 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineLocal reactions: severe0 Participants
LJEV and MVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineFever: 37.5-38.6°C38 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineLocal reactions: severe0 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineSystemic reactions: any122 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineFever: 37.5-38.6°C52 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineSystemic reaction: mild77 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineSystemic reaction: moderate42 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineSystemic reaction: severe3 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineFever: 38.7-39.9°C12 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineLocal reactions: any61 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineLocal reactions: mild50 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineFever: any64 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineLocal reactions: moderate11 Participants
MV Then LJEVNumber of Participants Experiencing Local and Systemic Reactogenicity After Receiving Measles VaccineFever: ≥ 40°C0 Participants
Secondary

Number of Participants Experiencing Unsolicited Adverse Events (AE)

Time frame: Up to 7 days post-vaccination

Population: Safety population

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
LJEV Then MVNumber of Participants Experiencing Unsolicited Adverse Events (AE)Serious adverse event2 Participants
LJEV Then MVNumber of Participants Experiencing Unsolicited Adverse Events (AE)Related adverse event0 Participants
LJEV Then MVNumber of Participants Experiencing Unsolicited Adverse Events (AE)Any Adverse Event35 Participants
LJEV and MVNumber of Participants Experiencing Unsolicited Adverse Events (AE)Serious adverse event0 Participants
LJEV and MVNumber of Participants Experiencing Unsolicited Adverse Events (AE)Any Adverse Event43 Participants
LJEV and MVNumber of Participants Experiencing Unsolicited Adverse Events (AE)Related adverse event4 Participants
MV Then LJEVNumber of Participants Experiencing Unsolicited Adverse Events (AE)Related adverse event2 Participants
MV Then LJEVNumber of Participants Experiencing Unsolicited Adverse Events (AE)Any Adverse Event79 Participants
MV Then LJEVNumber of Participants Experiencing Unsolicited Adverse Events (AE)Serious adverse event3 Participants
Secondary

Percentage of Participants With Seroprotection for Japanese Encephalitis 4 Weeks After Vaccination

Seroprotection after LJEV was defined as at least 1:10 dilution as recommended by the World Health Organization (WHO). JE antibody titers were determined by a plaque reduction neutralization test (PRNT).

Time frame: Day 0 (before vaccination) and Day 28 (4 weeks after LJEV vaccination)

Population: Per protocol population

ArmMeasureGroupValue (NUMBER)
LJEV Then MVPercentage of Participants With Seroprotection for Japanese Encephalitis 4 Weeks After VaccinationDay 03.4 percentage of participants
LJEV Then MVPercentage of Participants With Seroprotection for Japanese Encephalitis 4 Weeks After VaccinationDay 2892.1 percentage of participants
LJEV and MVPercentage of Participants With Seroprotection for Japanese Encephalitis 4 Weeks After VaccinationDay 05.4 percentage of participants
LJEV and MVPercentage of Participants With Seroprotection for Japanese Encephalitis 4 Weeks After VaccinationDay 2890.5 percentage of participants
MV Then LJEVPercentage of Participants With Seroprotection for Japanese Encephalitis 4 Weeks After VaccinationDay 06.1 percentage of participants
MV Then LJEVPercentage of Participants With Seroprotection for Japanese Encephalitis 4 Weeks After VaccinationDay 2890.6 percentage of participants

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026