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A Study of TAK-019 in Healthy Japanese Adults (COVID-19)

Primary Purpose

Prevention of Infection Disease Caused by Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2)

Status

Completed

Phase

Phase 1

Locations

Japan

Study Type

Interventional

Intervention

TAK-019

Placebo

About this trial

This is an interventional prevention trial for Prevention of Infection Disease Caused by Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2)

Eligibility Criteria

20 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

Healthy Japanese male and female adult participants aged >= 20 years of age at the time of signing of informed consent.
Participants who understand and are willing to comply with trial procedures and are available for the duration of follow-up.

Exclusion Criteria:

Participants who received any other SARS-CoV-2 or other experimental novel coronavirus vaccine prior to the trial.
Participants who have close contact of anyone known to have COVID-19 within 30 days prior to the trial vaccination.
Participants who were tested positive for SARS-CoV-2 prior to the trial or before the trial vaccination.
Participants who are on current treatment with other investigational agents for prophylaxis of COVID-19.
Participants who have traveled outside of Japan in the 30 days prior to the trial participation.
Participants with a clinically significant active infection (as assessed by the Investigator) or oral temperature >= 38 degree Celsius within 3 days of the intended date of vaccination.
Participants with known hypersensitivity or allergy to any of the investigational vaccine components.
Participants with history or any illness that, in the opinion of the Investigator, might interfere with the results of the trial or pose additional risk to the participants due to participation in the trial.
Participants with known or suspected impairment/alteration of immune function, including history of any autoimmune disease or neuro-inflammatory disease.
Abnormalities of splenic or thymic function.
Participants with a known bleeding diathesis, or any condition that may be associated with a prolonged bleeding time.
Participants with any serious chronic or progressive disease (eg, neoplasm, insulin dependent diabetes, cardiac, renal or hepatic disease).
Participants with body mass index (BMI) greater than or equal to 30 kg/m^2 (BMI= weight in kg/ height in meters^2).
Participants participating in any clinical trial with another investigational product within 30 days prior to the trial vaccination or intend to participate in another clinical trial at any time during the conduct of this trial.
Participants who received or plan to receive any other licensed vaccines within 14 days (for inactivated vaccines) or 28 days (for live vaccines) prior to trial dose administration.
Participants with acute or chronic clinically significant disease including pulmonary, cardiovascular, hepatic or renal abnormality evaluated by physical examination.
Participants involved in the trial conduct or their first degree relatives.
Participants who have history or infection of hepatitis B, hepatitis C, and human immunodeficiency virus infection.
Female participants who are pregnant or breastfeeding.

Sites / Locations

Sumida Hospital
Nishi Kumamoto Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

TAK-019

Placebo

Arm Description

TAK-019 0.5 mL, intramuscular injection in the upper arm

TAK-019 Matching Placebo, intramuscular injection in the upper arm

Outcomes

Primary Outcome Measures

Percentage of Participants With Solicited Local Adverse Events (AEs) for Six Subsequent Days Following First Vaccination

Solicited local AEs were pre-defined local (at the injection site) AEs for which participants were specifically questioned and which were noted by participants in their diary for six subsequent days following first vaccination. Solicited local AEs included injection site pain, tenderness, erythema/redness, induration, and swelling.

Percentage of Participants With Solicited Local AEs for Six Subsequent Days Following Second Vaccination

Solicited local AEs were pre-defined local (at the injection site) AEs for which participants were specifically questioned and which were noted by participants in their diary for six subsequent days following second vaccination. Solicited local AEs included injection site pain, tenderness, erythema/redness, induration, and swelling.

Percentage of Participants With Solicited Systemic AEs for Six Subsequent Days Following First Vaccination

Solicited systemic AEs were pre-defined AEs for which participants were specifically questioned and which were noted by participants in their diary for six subsequent days following first vaccination. Solicited systemic AEs included fever, fatigue, malaise, myalgia, arthralgia, nausea/vomiting and headache.

Percentage of Participants With Solicited Systemic AEs for Six Subsequent Days Following Second Vaccination

Solicited systemic AEs were pre-defined AEs for which participants were specifically questioned and which were noted by participants in their diary for six subsequent days following second vaccination. Solicited systemic AEs included fever, fatigue, malaise, myalgia, arthralgia, nausea/vomiting and headache.

Percentage of Participants With Unsolicited AEs for 20 Days Following First Vaccination

Unsolicited AEs were all AEs that were not pre-defined for which the participant was not specifically questioned in the participant diary.

Percentage of Participants With Unsolicited AEs for 27 Days Following Second Vaccination

Unsolicited AEs were all AEs that were not pre-defined for which the participant was not specifically questioned in the participant diary.

Percentage of Participants With Serious Adverse Events (SAEs) Until Day 50

Only unsolicited SAEs data was planned to be collected and assessed for the assessment of this outcome measure (OM) and solicited SAE was out of the scope of assessment. Unsolicited SAEs were those AEs that were not pre-defined for which the participant was not specifically questioned in the participant diary. Percentage of participants with unsolicited SAEs until Day 50 were reported in this outcome measure.

Percentage of Participants With Adverse Events of Special Interest (AESI) Until Day 50

AESIs were defined as AEs that were specifically highlighted to the Investigator. Only unsolicited AESI data was planned to be collected and assessed for the assessment of this OM and solicited AESI was out of the scope of assessment. Unsolicited AESIs were those AEs that were not pre-defined for which the participant was not specifically questioned in the participant diary. Percentage of participants with unsolicited AESIs until Day 50 were reported in this outcome measure.

Percentage of Participants With Medically-Attended Adverse Events (MAAEs) Until Day 50

MAAEs are defined as AEs leading to an unscheduled visit to or by a healthcare professional including visits to an emergency department, but not fulfilling seriousness criteria. Only unsolicited MAAEs data was planned to be collected and assessed for the assessment of this OM and solicited MAAE was out of the scope of assessment. Unsolicited MAAEs were those AEs that were not pre-defined for which the participant was not specifically questioned in the participant diary. Percentage of participants with unsolicited MAAEs until Day 50 were reported in this outcome measure.

Percentage of Participants With Any AE Leading to Discontinuation of Vaccination

Only any unsolicited AE leading to discontinuation of vaccination data was planned to be collected and assessed for the assessment of this OM and solicited AE leading to discontinuation of vaccination was out of the scope of assessment. Unsolicited AEs were those AEs that were not pre-defined for which the participant was not specifically questioned in the participant diary. Percentage of participants with any unsolicited AE leading to discontinuation of vaccination until Day 22 were reported in this outcome measure.

Percentage of Participants With Any AE Leading to Participant's Withdrawal From the Trial Until Day 50

Only any unsolicited AE leading to participant's withdrawal from the trial data was planned to be collected and assessed for the assessment of this OM and solicited AE leading to participant's withdrawal from the trial was out of the scope of assessment. Unsolicited AEs were those AEs that were not pre-defined for which the participant was not specifically questioned in the participant diary. Percentage of participants with any unsolicited AE leading to participant's withdrawal from the trial until Day 50 were reported in this outcome measure.

Percentage of Participants With Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) Infection Until Day 50

Geometric Mean Titers (GMT) of Serum Immunoglobulin G (IgG) Antibody Levels to SARS-CoV-2 Recombinant Spike (rS) Protein on Day 36

GMT was the immunogenicity outcome expressed as reciprocal antibody titer with average for each group. Titer values was measured as below lower limit of quantification (LLOQ) were imputed to a value that was half of the LLOQ. LLOQ was equal to 200. Here, ELISA is Enzyme-linked immunosorbent assay.

Geometric Mean Fold Rise (GMFR) of Serum IgG Antibody Levels to SARS-CoV-2 rS Protein on Day 36

GMFR was calculated as the ratio of the post-vaccination titer level to the baseline titer level. Baseline was defined as the last measurement taken before the first dose of study intervention.

Seroconversion Rate (SCR) of Serum IgG Antibody Levels to SARS-CoV-2 rS Protein on Day 36

SCR was defined as percentage of participants with 4-fold or more rises in titer if naive at baseline OR percentage of participants with 2-fold or more rises in titer if seropositive at baseline. Baseline was defined as the last measurement taken before the first dose of study intervention.

Seroresponse Rate (SRR) of Serum IgG Antibody Levels to SARS-CoV-2 rS Protein on Day 36

SRR was defined as percentage of participants with greater than or equal to (>=) 95 percentile in titer at Baseline for all participants. Baseline was defined as the last measurement taken before the first dose of study intervention.

Secondary Outcome Measures

Percentage of Participants With SAE Throughout the Trial

Only unsolicited SAEs data was planned to be collected and assessed for the assessment of this OM and solicited SAE was out of the scope of assessment. Unsolicited SAEs were those AEs that were not pre-defined for which the participant was not specifically questioned in the participant diary. Percentage of participants with unsolicited SAEs throughout the trial were reported in this outcome measure.

Percentage of Participants With AESI Throughout the Trial

AESIs were defined as AEs that were specifically highlighted to the Investigator. Only unsolicited AESI data was planned to be collected and assessed for the assessment of this OM and solicited AESI was out of the scope of assessment. Unsolicited AESI were those AEs that were not pre-defined for which the participant was not specifically questioned in the participant diary. Percentage of participants with unsolicited AESIs throughout the trial were reported in this outcome measure.

Percentage of Participants With MAAEs Throughout the Trial

MAAEs are defined as AEs leading to an unscheduled visit to or by a healthcare professional including visits to an emergency department, but not fulfilling seriousness criteria. Only unsolicited MAAEs data was planned to be collected and assessed for the assessment of this OM and solicited MAAE was out of the scope of assessment. Unsolicited MAAEs were those AEs that were not pre-defined for which the participant was not specifically questioned in the participant diary. Percentage of participants with unsolicited MAAEs throughout the trial were reported in this outcome measure.

Percentage of Participants With Any AE Leading to Participant's Withdrawal From the Trial From the Day of Vaccination Throughout the Trial

Only any unsolicited AE leading to participant's withdrawal from the trial data was planned to be collected and assessed for the assessment of this OM and solicited AE leading to participant's withdrawal from the trial was out of the scope of assessment. Unsolicited AEs were those AEs that were not pre-defined for which the participant was not specifically questioned in the participant diary. Percentage of participants with any unsolicited AE leading to withdrawal from the trial from the day of vaccination throughout the trial were reported in this outcome measure.

Percentage of Participants With SARS-CoV-2 Infection Throughout the Trial

GMT of Serum IgG Antibody Levels to SARS-CoV-2 rS Protein on Days 22, 50, 202, and 387

GMT was the immunogenicity outcome expressed as reciprocal antibody titer with average for each group. Titer values was measured as below LLOQ were imputed to a value that was half of the LLOQ. GMT of serum IgG antibody levels to the SARS-CoV-2 rS protein was measured where LLOQ was equal to 200.

GMFR of Serum IgG Antibody Levels to SARS-CoV-2 rS Protein on Days 22, 50, 202, and 387

GMFR was calculated as the ratio of the post-vaccination titer level to the baseline titer level. Where baseline was defined as the last measurement taken before the first dose of study intervention.

SCR of Serum IgG Antibody Levels to SARS-CoV-2 rS Protein on Days 22, 50, 202, and 387

SRR of Serum IgG Antibody Levels to SARS-CoV-2 rS Protein on Days 22, 50, 202, and 387

SRR was defined as percentage of participants with >=95 percentile in titer at Baseline for all participants. Baseline was defined as the last measurement taken before the first dose of study intervention.

GMT of Serum Neutralizing Antibody (nAb) Titers to Wild Type Virus on Days 22, 36, 50, 202 and Day 387

The neutralization titer was expressed as the reciprocal of the highest dilution at which greater than or equal to (>=) 50% of the replicate wells were protected from infection (MN50). GMT was the immunogenicity outcome expressed as reciprocal antibody titer with average for each group. Titer values was measured as below LLOQ were imputed to a value that was half of the LLOQ. GMT of serum IgG antibody levels to the SARS-CoV-2 rS protein was measured where LLOQ was equal to 20.

GMFR of Serum nAb Titers to Wild Type Virus on Days 22, 36, 50, 202 and 387

The neutralization titer was expressed as the reciprocal of the highest dilution at which >=50% of the replicate wells were protected from infection (MN50). GMFR was calculated as the ratio of the post-vaccination titer level to the baseline titer level. Baseline was defined as the last measurement taken before the first dose of study intervention.

SCR to Serum nAb Titers to Wild Type Virus on Days 22, 36, 50, 202 and 387

The neutralization titer was expressed as the reciprocal of the highest dilution at which >=50% of the replicate wells were protected from infection (MN50). SCR was defined as percentage of participants with 4-fold or more rises in titer if naive at baseline OR percentage of participants with 2-fold or more rises in titer if seropositive at Baseline. Baseline was defined as the last measurement taken before the first dose of study intervention.

SRR to Serum nAb Titers to Wild Type Virus on Days 22, 36, 50, 202 and 387

The neutralization titer was expressed as the reciprocal of the highest dilution at which >=50% of the replicate wells were protected from infection (MN50). SRR was defined as percentage of participants with >=95 percentile in titer at Baseline for all participants. Baseline was defined as the last measurement taken before the first dose of study intervention.

Full Information

NCT ID

NCT04712110

First Posted

January 14, 2021

Last Updated

May 12, 2023

Sponsor

Takeda

1. Study Identification

Unique Protocol Identification Number

NCT04712110

Brief Title

A Study of TAK-019 in Healthy Japanese Adults (COVID-19)

Official Title

A Phase 1/2, Randomized, Observer-Blind, Placebo-Controlled Trial to Evaluate the Safety and Immunogenicity of TAK-019 by Intramuscular Injection in Healthy Japanese Male and Female Adults Aged 20 Years and Older (COVID-19)

Study Type

Interventional

2. Study Status

Record Verification Date

May 2023

Overall Recruitment Status

Completed

Study Start Date

February 12, 2021 (Actual)

Primary Completion Date

March 28, 2022 (Actual)

Study Completion Date

March 28, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title

Sponsor

Name of the Sponsor

Takeda

4. Oversight

Studies a U.S. FDA-regulated Drug Product

Yes

Studies a U.S. FDA-regulated Device Product

Product Manufactured in and Exported from the U.S.

Yes

Data Monitoring Committee

5. Study Description

Brief Summary

TAK-019 is a vaccine in development to protect people against Covid-19. The main aims of the study are to learn if TAK-019 can protect people from Covid-19 and to check for side effects from TAK-019. At the first visit, the study doctor will check if each person can take part. Those who can take part will be chosen for 1 of 2 treatments by chance. Participants will either receive an injection of TAK-019 or a placebo in their arm. In this study, a placebo will look like the TAK-019 vaccine but will not have any medicine in it. 3 times as many participants will receive TAK-019 than placebo. Participants will receive 2 injections of TAK-019 or placebo, 21 days apart. Participants will be asked to record their temperature and any medical problems in an electronic diary for up to 7 days after each injection. During the study, participants will visit the clinic for regular check-ups, blood tests, and sometimes for nose swab samples. When all participants have attended a clinic visit 28 days after their 2nd injection, the study sponsor (Takeda) will check how many participants have made enough antibodies to protect them against Covid-19. The participants will stay in the study for up to 12 months after they have had their 2nd injection. During this time, the study doctors will continue to check how many participants have made enough antibodies to protect them against Covid-19. Also, they will check if participants have any more side effects from TAK-019 or the placebo.

Detailed Description

The drug being tested in this study is called TAK-019. TAK-019 is being tested to prevent infectious disease caused by Severe Acute Respiratory Syndrome coronavirus-2 (SARS-CoV-2). This study will look at the evaluate the safety and immunogenicity of 2 doses of TAK-019 by intramuscular (IM) injection 21 days apart in healthy Japanese male and female adults. The study will enroll approximately 200 healthy volunteers. Participants will be randomly assigned (by chance, like flipping a coin) to one of the two treatment groups-which will remain undisclosed to the participant and study doctor during the study (unless there is an urgent medical need): TAK-019 0.5 mL Placebo- this is an injection that looks like the study drug but has no active ingredient All participants will be asked to take intramuscular injection in the upper arm twice throughout the study. This multi-center trial will be conducted in Japan. The overall time to participate in this study is 12 months from the second vaccination (totally 387 days). Participants will make multiple visits to the clinic and will be contacted by telephone or a final visit after the last vaccination for a follow-up assessment.

6. Conditions and Keywords

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

Prevention of Infection Disease Caused by Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2)

7. Study Design

Primary Purpose

Prevention

Study Phase

Phase 1, Phase 2

Interventional Study Model

Parallel Assignment

Masking

ParticipantCare ProviderInvestigatorOutcomes Assessor

Allocation

Randomized

Enrollment

200 (Actual)

8. Arms, Groups, and Interventions

Arm Title

TAK-019

Arm Type

Experimental

Arm Description

TAK-019 0.5 mL, intramuscular injection in the upper arm

Arm Title

Placebo

Arm Type

Placebo Comparator

Arm Description

TAK-019 Matching Placebo, intramuscular injection in the upper arm

Intervention Type

Biological

Intervention Name(s)

TAK-019

Intervention Description

TAK-019 intramuscular injection

Intervention Type

Biological

Intervention Name(s)

Placebo

Intervention Description

Placebo intramuscular injection

Primary Outcome Measure Information:

Title

Percentage of Participants With Solicited Local Adverse Events (AEs) for Six Subsequent Days Following First Vaccination

Description

Time Frame

Up to Day 7 (6 subsequent days after first vaccination on Day 1)

Title

Percentage of Participants With Solicited Local AEs for Six Subsequent Days Following Second Vaccination

Description

Solicited local AEs were pre-defined local (at the injection site) AEs for which participants were specifically questioned and which were noted by participants in their diary for six subsequent days following second vaccination. Solicited local AEs included injection site pain, tenderness, erythema/redness, induration, and swelling.

Time Frame

Up to Day 28 (6 subsequent days after second vaccination on Day 22)

Title

Percentage of Participants With Solicited Systemic AEs for Six Subsequent Days Following First Vaccination

Description

Time Frame

Up to Day 7 (6 subsequent days after first vaccination on Day 1)

Title

Percentage of Participants With Solicited Systemic AEs for Six Subsequent Days Following Second Vaccination

Description

Solicited systemic AEs were pre-defined AEs for which participants were specifically questioned and which were noted by participants in their diary for six subsequent days following second vaccination. Solicited systemic AEs included fever, fatigue, malaise, myalgia, arthralgia, nausea/vomiting and headache.

Time Frame

Up to Day 28 (6 subsequent days after second vaccination on Day 22)

Title

Percentage of Participants With Unsolicited AEs for 20 Days Following First Vaccination

Description

Unsolicited AEs were all AEs that were not pre-defined for which the participant was not specifically questioned in the participant diary.

Time Frame

Up to Day 21 (20 days after first vaccination on Day 1)

Title

Percentage of Participants With Unsolicited AEs for 27 Days Following Second Vaccination

Description

Unsolicited AEs were all AEs that were not pre-defined for which the participant was not specifically questioned in the participant diary.

Time Frame

Up to Day 49 (27 days after second vaccination on Day 22)

Title

Percentage of Participants With Serious Adverse Events (SAEs) Until Day 50

Description

Time Frame

Day 1 up to Day 50

Title

Percentage of Participants With Adverse Events of Special Interest (AESI) Until Day 50

Description

Time Frame

Day 1 up to Day 50

Title

Percentage of Participants With Medically-Attended Adverse Events (MAAEs) Until Day 50

Description

Time Frame

Day 1 up to Day 50

Title

Percentage of Participants With Any AE Leading to Discontinuation of Vaccination

Description

Time Frame

Day 1 up to Day 22

Title

Percentage of Participants With Any AE Leading to Participant's Withdrawal From the Trial Until Day 50

Description

Time Frame

Day 1 up to Day 50

Title

Percentage of Participants With Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) Infection Until Day 50

Time Frame

Day 1 up to Day 50

Title

Geometric Mean Titers (GMT) of Serum Immunoglobulin G (IgG) Antibody Levels to SARS-CoV-2 Recombinant Spike (rS) Protein on Day 36

Description

Time Frame

At Day 36

Title

Geometric Mean Fold Rise (GMFR) of Serum IgG Antibody Levels to SARS-CoV-2 rS Protein on Day 36

Description

GMFR was calculated as the ratio of the post-vaccination titer level to the baseline titer level. Baseline was defined as the last measurement taken before the first dose of study intervention.

Time Frame

At Day 36

Title

Seroconversion Rate (SCR) of Serum IgG Antibody Levels to SARS-CoV-2 rS Protein on Day 36

Description

Time Frame

At Day 36

Title

Seroresponse Rate (SRR) of Serum IgG Antibody Levels to SARS-CoV-2 rS Protein on Day 36

Description

Time Frame

At Day 36

Secondary Outcome Measure Information:

Title

Percentage of Participants With SAE Throughout the Trial

Description

Time Frame

Day 1 up to Day 387

Title

Percentage of Participants With AESI Throughout the Trial

Description

AESIs were defined as AEs that were specifically highlighted to the Investigator. Only unsolicited AESI data was planned to be collected and assessed for the assessment of this OM and solicited AESI was out of the scope of assessment. Unsolicited AESI were those AEs that were not pre-defined for which the participant was not specifically questioned in the participant diary. Percentage of participants with unsolicited AESIs throughout the trial were reported in this outcome measure.

Time Frame

Day 1 up to Day 387

Title

Percentage of Participants With MAAEs Throughout the Trial

Description

MAAEs are defined as AEs leading to an unscheduled visit to or by a healthcare professional including visits to an emergency department, but not fulfilling seriousness criteria. Only unsolicited MAAEs data was planned to be collected and assessed for the assessment of this OM and solicited MAAE was out of the scope of assessment. Unsolicited MAAEs were those AEs that were not pre-defined for which the participant was not specifically questioned in the participant diary. Percentage of participants with unsolicited MAAEs throughout the trial were reported in this outcome measure.

Time Frame

Day 1 up to Day 387

Title

Percentage of Participants With Any AE Leading to Participant's Withdrawal From the Trial From the Day of Vaccination Throughout the Trial

Description

Only any unsolicited AE leading to participant's withdrawal from the trial data was planned to be collected and assessed for the assessment of this OM and solicited AE leading to participant's withdrawal from the trial was out of the scope of assessment. Unsolicited AEs were those AEs that were not pre-defined for which the participant was not specifically questioned in the participant diary. Percentage of participants with any unsolicited AE leading to withdrawal from the trial from the day of vaccination throughout the trial were reported in this outcome measure.

Time Frame

Day 1 up to Day 387

Title

Percentage of Participants With SARS-CoV-2 Infection Throughout the Trial

Time Frame

Day 1 up to Day 387

Title

GMT of Serum IgG Antibody Levels to SARS-CoV-2 rS Protein on Days 22, 50, 202, and 387

Description

Time Frame

At Days 22, 50, 202, and 387

Title

GMFR of Serum IgG Antibody Levels to SARS-CoV-2 rS Protein on Days 22, 50, 202, and 387

Description

GMFR was calculated as the ratio of the post-vaccination titer level to the baseline titer level. Where baseline was defined as the last measurement taken before the first dose of study intervention.

Time Frame

At Days 22, 50, 202, and 387

Title

SCR of Serum IgG Antibody Levels to SARS-CoV-2 rS Protein on Days 22, 50, 202, and 387

Description

Time Frame

At Days 22, 50, 202, and 387

Title

SRR of Serum IgG Antibody Levels to SARS-CoV-2 rS Protein on Days 22, 50, 202, and 387

Description

Time Frame

At Days 22, 50, 202, and 387

Title

GMT of Serum Neutralizing Antibody (nAb) Titers to Wild Type Virus on Days 22, 36, 50, 202 and Day 387

Description

Time Frame

At Days 22, 36, 50, 202 and 387

Title

GMFR of Serum nAb Titers to Wild Type Virus on Days 22, 36, 50, 202 and 387

Description

Time Frame

At Days 22, 36, 50, 202 and 387

Title

SCR to Serum nAb Titers to Wild Type Virus on Days 22, 36, 50, 202 and 387

Description

Time Frame

At Days 22, 36, 50, 202 and 387

Title

SRR to Serum nAb Titers to Wild Type Virus on Days 22, 36, 50, 202 and 387

Description

Time Frame

At Days 22, 36, 50, 202 and 387

10. Eligibility

Sex

All

Minimum Age & Unit of Time

20 Years

Accepts Healthy Volunteers

Eligibility Criteria

Inclusion Criteria: Healthy Japanese male and female adult participants aged >= 20 years of age at the time of signing of informed consent. Participants who understand and are willing to comply with trial procedures and are available for the duration of follow-up. Exclusion Criteria: Participants who received any other SARS-CoV-2 or other experimental novel coronavirus vaccine prior to the trial. Participants who have close contact of anyone known to have COVID-19 within 30 days prior to the trial vaccination. Participants who were tested positive for SARS-CoV-2 prior to the trial or before the trial vaccination. Participants who are on current treatment with other investigational agents for prophylaxis of COVID-19. Participants who have traveled outside of Japan in the 30 days prior to the trial participation. Participants with a clinically significant active infection (as assessed by the Investigator) or oral temperature >= 38 degree Celsius within 3 days of the intended date of vaccination. Participants with known hypersensitivity or allergy to any of the investigational vaccine components. Participants with history or any illness that, in the opinion of the Investigator, might interfere with the results of the trial or pose additional risk to the participants due to participation in the trial. Participants with known or suspected impairment/alteration of immune function, including history of any autoimmune disease or neuro-inflammatory disease. Abnormalities of splenic or thymic function. Participants with a known bleeding diathesis, or any condition that may be associated with a prolonged bleeding time. Participants with any serious chronic or progressive disease (eg, neoplasm, insulin dependent diabetes, cardiac, renal or hepatic disease). Participants with body mass index (BMI) greater than or equal to 30 kg/m^2 (BMI= weight in kg/ height in meters^2). Participants participating in any clinical trial with another investigational product within 30 days prior to the trial vaccination or intend to participate in another clinical trial at any time during the conduct of this trial. Participants who received or plan to receive any other licensed vaccines within 14 days (for inactivated vaccines) or 28 days (for live vaccines) prior to trial dose administration. Participants with acute or chronic clinically significant disease including pulmonary, cardiovascular, hepatic or renal abnormality evaluated by physical examination. Participants involved in the trial conduct or their first degree relatives. Participants who have history or infection of hepatitis B, hepatitis C, and human immunodeficiency virus infection. Female participants who are pregnant or breastfeeding.

Overall Study Officials:

First Name & Middle Initial & Last Name & Degree

Study Director

Organizational Affiliation

Takeda

Official's Role

Study Director

Facility Information:

Facility Name

Sumida Hospital

City

Sumida-ku

State/Province

Tokyo

Country

Japan

Facility Name

Nishi Kumamoto Hospital

City

Kumamoto

Country

Japan

12. IPD Sharing Statement

Plan to Share IPD

Yes

IPD Sharing Plan Description

Takeda provides access to the de-identified individual participant data (IPD) for eligible studies to aid qualified researchers in addressing legitimate scientific objectives (Takeda's data sharing commitment is available on https://clinicaltrials.takeda.com/takedas-commitment?commitment=5). These IPDs will be provided in a secure research environment following approval of a data sharing request, and under the terms of a data sharing agreement.

IPD Sharing Access Criteria

IPD from eligible studies will be shared with qualified researchers according to the criteria and process described on https://vivli.org/ourmember/takeda/. For approved requests, the researchers will be provided access to anonymized data (to respect patient privacy in line with applicable laws and regulations) and with information necessary to address the research objectives under the terms of a data sharing agreement.

IPD Sharing URL

https://vivli.org/ourmember/takeda/

Citations:

PubMed Identifier

35501178

Citation

Masuda T, Murakami K, Sugiura K, Sakui S, Schuring RP, Mori M. Safety and immunogenicity of NVX-CoV2373 (TAK-019) vaccine in healthy Japanese adults: Interim report of a phase I/II randomized controlled trial. Vaccine. 2022 May 26;40(24):3380-3388. doi: 10.1016/j.vaccine.2022.04.035. Epub 2022 Apr 29.

Results Reference

derived

Links:

URL

https://clinicaltrials.takeda.com/study-detail/60084996565ce300294c6ad7

Description

To obtain more information on the study, click here/on this link

Learn more about this trial

A Study of TAK-019 in Healthy Japanese Adults (COVID-19)

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