| Eligibility |
Inclusion Criteria:
Age and Sex:
1. Participants aged 18 years or older (or the minimum age of consent in accordance with
local regulations) at screening.
2. Healthy female participants of nonchildbearing potential and/or male participants who
are overtly healthy as determined by medical evaluation including medical history,
physical examination, and laboratory tests.
Other Inclusion Criteria:
3. BMI of 16-32 kg/m2; and a total body weight >45 kg (99 lb).
Exclusion Criteria:
Medical Conditions:
1. Evidence or history of clinically significant hematological, renal, endocrine,
pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurological, or
allergic disease (including drug allergies, but excluding untreated, asymptomatic,
seasonal allergies at the time of dosing).
- Any condition possibly affecting drug absorption (eg, gastrectomy,
cholecystectomy).
- History of HIV infection, hepatitis B, or hepatitis C; positive testing for HIV,
HBsAg, HBcAb, or HCVAb. Hepatitis B vaccination is allowed.
- Hypersensitivity to any component of the formulations.
2. Any medical or psychiatric condition including recent (within the past year) or active
suicidal ideation/behavior or laboratory abnormality or other conditions that may
increase the risk of study participation or, in the investigator's judgment, make the
participant inappropriate for the study.
Prior/Concomitant Therapy:
3. Use of prescription or nonprescription drugs and dietary and herbal supplements within
7 days or 5 half lives (whichever is longer) prior to the first dose of study
intervention.
4. Current use of any prohibited concomitant medication(s) or participant unwilling or
unable to use a required concomitant medication(s).
Prior/Concurrent Clinical Study Experience:
5. Previous administration of an investigational product (drug or vaccine) within 30 days
(or as determined by the local requirement) or 5 half lives preceding the first dose
of study intervention used in this study (whichever is longer).
Diagnostic Assessments:
6. A positive urine drug test. A single repeat for positive drug screen may be allowed.
7. Screening supine BP =140 mm Hg (systolic) or =90 mm Hg (diastolic) for participants
<60 years; and =150/90 mm/Hg for participants =60 years old, following at least 5
minutes of supine rest. If systolic BP is =140 or 150 mm Hg (based on age) or
diastolic =90 mm Hg, the BP should be repeated 2 more times and the average of the 3
BP values should be used to determine the participant's eligibility.
8. Standard 12 lead ECG that demonstrates clinically relevant abnormalities that may
affect participant safety or interpretation of study results (eg, QTcF >450 ms,
complete LBBB, signs of an acute or indeterminate age myocardial infarction, ST-T
interval changes suggestive of myocardial ischemia, second or third degree AV block,
or serious bradyarrhythmias or tachyarrhythmias). If QTcF exceeds 450 ms, or QRS
exceeds 120 ms, the ECG should be repeated twice and the average of the 3 QTcF or QRS
values used to determine the participant's eligibility. Computer-interpreted ECGs
should be overread by a physician experienced in reading ECGs before excluding a
participant.
9. Renal impairment as defined by an eGFR of <60 mL/min/1.73 m².
10. Participants with ANY of the following abnormalities in clinical laboratory tests at
screening, as assessed by the study specific laboratory and confirmed by a single
repeat test, if deemed necessary:
• ALT, AST, Bilirubin =1.5 × ULN. Participants with a history of Gilbert's syndrome
may have direct bilirubin measured and would be eligible for this study provided the
direct bilirubin level is =ULN.
Other Exclusion Criteria:
11. History of alcohol abuse or binge drinking and/or any other illicit drug use or
dependence within 6 months of Screening. Binge drinking is defined as a pattern of 5
(male) and 4 (female) or more alcoholic drinks in about 2 hours. As a general rule,
alcohol intake should not exceed 14 units per week (1 unit = 8 ounces (240 mL) beer, 1
ounce (30 mL) of 40% spirit, or 3 ounces (90 mL) of wine).
12. Unwilling or unable to comply with the criteria in the Lifestyle Considerations
section of this protocol.
13. Investigator site staff directly involved in the conduct of the study and their family
members, site staff otherwise supervised by the investigator, and sponsor and sponsor
delegate employees directly involved in the conduct of the study and their family
members.
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