inclusion criteria: * male and female participant of 60 years of age or older, at the time of signing the informed consent. * participants who are generally healthy. note: healthy participant is defined as an individual who is in good general health, not having any symptomatic mental or physical disorder requiring regular or frequent medication. subjects can be enrolled if the regular or frequent medication keeps the condition well controlled and asymptomatic with the treatment according to the investigator's discretion. * body mass index (bmi) within the range 18.0 and ≤35.0 kg m2 (inclusive). * capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (icf) and in the protocol.

inclusion criteria: * male and female participant of 60 years of age or older, at the time of signing the informed consent. * participants who are generally healthy. note: healthy participant is defined as an individual who is in good general health, not having any symptomatic mental or physical disorder requiring regular or frequent medication. subjects can be enrolled if the regular or frequent medication keeps the condition well controlled and asymptomatic with the treatment according to the investigator's discretion. * body mass index (bmi) within the range 18.0 and ≤35.0 kg m2 (inclusive). * capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (icf) and in the protocol.

inclusion criteria: - male and female participant of 60 years of age or older, at the time of signing the informed consent. - participants who are generally healthy. note: healthy participant is defined as an individual who is in good general health, not having any symptomatic mental or physical disorder requiring regular or frequent medication. subjects can be enrolled if the regular or frequent medication keeps the condition well controlled and asymptomatic with the treatment according to the investigator's discretion. - body mass index (bmi) within the range 18.0 and ≤35.0 kg m2 (inclusive). - capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (icf) and in the protocol.

inclusion criteria: - male and female participant of 60 years of age or older, at the time of signing the informed consent. - participants who are generally healthy. note: healthy participant is defined as an individual who is in good general health, not having any symptomatic mental or physical disorder requiring regular or frequent medication. subjects can be enrolled if the regular or frequent medication keeps the condition well controlled and asymptomatic with the treatment according to the investigator's discretion. - body mass index (bmi) within the range 18.0 and ≤35.0 kg m2 (inclusive). - capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (icf) and in the protocol.