Created at Source Raw Value Validated value
June 25, 2024, noon usa

inclusion criteria: 1. clinically healthy subjects within the following age groups: adults (18-59 years) and elderly (60 years and above. 2. subjects have been informed properly regarding the study and signed the informed consent form. 3. subjects will commit to comply with the instructions of the investigator and the schedule of the trial.

inclusion criteria: 1. clinically healthy subjects within the following age groups: adults (18-59 years) and elderly (60 years and above. 2. subjects have been informed properly regarding the study and signed the informed consent form. 3. subjects will commit to comply with the instructions of the investigator and the schedule of the trial.

Nov. 16, 2021, 6:30 p.m. usa

inclusion criteria: clinically healthy subjects within the following age groups: adults (18-59 years) and elderly (60 years and above. subjects have been informed properly regarding the study and signed the informed consent form. subjects will commit to comply with the instructions of the investigator and the schedule of the trial.

inclusion criteria: clinically healthy subjects within the following age groups: adults (18-59 years) and elderly (60 years and above. subjects have been informed properly regarding the study and signed the informed consent form. subjects will commit to comply with the instructions of the investigator and the schedule of the trial.

Oct. 6, 2021, 11:30 a.m. usa

inclusion criteria: 1. clinically healthy subjects within the following age groups: adults (18-59 years) and elderly (60 years and above. 2. subjects have been informed properly regarding the study and signed the informed consent form. 3. subjects will commit to comply with the instructions of the investigator and the schedule of the trial.

inclusion criteria: 1. clinically healthy subjects within the following age groups: adults (18-59 years) and elderly (60 years and above. 2. subjects have been informed properly regarding the study and signed the informed consent form. 3. subjects will commit to comply with the instructions of the investigator and the schedule of the trial.