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

inclusion criteria: * japanese male or female participants between the ages of 20 and 85 years, inclusive, at randomization. * participants who are willing and able to comply with all scheduled visits, vaccination plan, laboratory tests, lifestyle considerations, and other study procedures. * healthy participants who are determined by medical history, physical examination, and clinical judgment of the investigator to be eligible for inclusion in the study. * capable of giving personal signed informed consent.

inclusion criteria: * japanese male or female participants between the ages of 20 and 85 years, inclusive, at randomization. * participants who are willing and able to comply with all scheduled visits, vaccination plan, laboratory tests, lifestyle considerations, and other study procedures. * healthy participants who are determined by medical history, physical examination, and clinical judgment of the investigator to be eligible for inclusion in the study. * capable of giving personal signed informed consent.

Oct. 26, 2020, 11:31 p.m. usa

inclusion criteria: - japanese male or female participants between the ages of 20 and 85 years, inclusive, at randomization. - participants who are willing and able to comply with all scheduled visits, vaccination plan, laboratory tests, lifestyle considerations, and other study procedures. - healthy participants who are determined by medical history, physical examination, and clinical judgment of the investigator to be eligible for inclusion in the study. - capable of giving personal signed informed consent.

inclusion criteria: - japanese male or female participants between the ages of 20 and 85 years, inclusive, at randomization. - participants who are willing and able to comply with all scheduled visits, vaccination plan, laboratory tests, lifestyle considerations, and other study procedures. - healthy participants who are determined by medical history, physical examination, and clinical judgment of the investigator to be eligible for inclusion in the study. - capable of giving personal signed informed consent.