Single and Multiple Ascending Doses Clinical Pharmacology Study With KAR5585

The purpose of this study is to explore the safety, tolerability, pharmacokinetics (PK), and
cardiac conduction effects of single and multiple ascending doses of KAR5585 in healthy
adults. Food effect will also be evaluated after a single-dose administration.

Inclusion Criteria:

- Subject is able to read, write, and comprehend English at a sufficient level to
understand study-related materials

- Subject is able to provide written informed consent and to comply with all study
requirements and restrictions

- Subject is male or female and aged 18 to 65 years, inclusive, at the time of informed
consent

- Subject is in good health as determined by the PI based on detailed medical history,
physical examination, vital signs, clinical laboratory tests, ECGs, and other
pre-dose evaluations

- Subject agrees to use a medically acceptable form of birth control from CRU admission
until at least 30 days (female subject) or 90 days (male subject) after the last dose
of study drug. Males will also not donate sperm from CRU admission until at least 90
days after the last dose of study drug. If a subject is not sexually active but
becomes active during study participation, the subject agrees they and their partner
will use a medically accepted form of contraception for the time specified. Medically
acceptable forms of contraception are:

- FDA-approved female hormonal contraceptives used consistently for 2 or more
cycles before Screening, including oral contraceptives, intrauterine device
(IUD), medroxyprogesterone acetate injection (Depo Provera®), hormonal implant
(Norplant®, Implanon®, Nexplanon®), and vaginal ring (NuvaRing®)

- Male condom plus spermicide

- Male condom plus contraceptive sponge, foam, or jelly

- Female condom plus spermicide

- Diaphragm with spermicide plus male condom

- Cervical cap with spermicide plus male condom

- Surgical sterilization of the subject or partner (vasectomy for males,
hysterectomy or bilateral oophorectomy for females)

- Abstinence

- If female, subject agrees that a serum pregnancy test ([β hCG] beta human chorionic
gonadotropin ) will be performed at Screening, on Day 2 (CRU admission), and at the
last study visit and negative test results at Screening and CRU admission are
required to be considered for study participation

- Subject has a body mass index (BMI) of 20 to 35 kg/m2, inclusive, and body weight <
120 kg at Screening

Exclusion Criteria:

- Subject currently uses tobacco or nicotine-containing products or has used such
products within 6 months before CRU admission

- Subject has history or current evidence of any clinically significant cardiac,
endocrinologic, hematologic, hepatobiliary, immunologic, metabolic, urologic,
pulmonary, neurologic, dermatologic, psychiatric, renal, or other major disease, as
determined by the PI

- Subject has a history of cancer within 5 years before CRU admission (excluding
non-melanoma skin cancer)

- Subject has a history of autonomic dysfunction (eg, history of repeated dizziness,
fainting, or symptomatic orthostatic hypotension)

- Subject has a history of risk factors for torsades de pointes, including unexplained
syncope, known long QT syndrome, heart failure, myocardial infarction, angina, OR
clinically significant abnormal laboratory assessments including hypokalemia,
hypomagnesemia, or hypercalcemia OR has a family history of long QT syndrome or
Brugada syndrome

- Subject has 1 or more clinically significant abnormal laboratory test values (as
determined by the PI)

- Subject has an uninterpretable or abnormal screening ECG indicating a second- or
third-degree atrioventricular block, or 1 or more of the following: QRS interval
(ventricular depolarization) > 110 msec; a PR interval (atrioventricular conduction)
> 220 msec, or QTc (corrected QT interval) of ≥ 450 msec (for male) or ≥ 470 msec
(for female) or any rhythm other than sinus rhythm that is interpreted by the PI or a
qualified designee to be clinically significant

- Subject has a resting heart rate (HR) of < 40 beats/min or > 90 beats/min at
Screening or on CRU admission

- Subject has a sustained supine systolic blood pressure (BP) > 155 or < 90 mm Hg or a
supine diastolic BP > 95 or < 50 mm Hg at Screening or upon CRU admission. Blood
pressure in the supine position may be retested once and 'sustained' is defined as
the parameter (either systolic or diastolic BP) being outside the stated limits at
both assessments.

- Subject participates in another clinical trial or treatment with an investigational
agent within 30 days or 5 half-lives, whichever is longer, before CRU admission

- Subject has a history of alcohol or drug abuse or dependence within 12 months before
CRU admission, as determined by the PI

- Subject has a clinically significant infection within 3 months before CRU admission,
as determined by the PI

- Subject has any condition that, in the opinion of the PI, would make the subject
unsuitable for enrollment or could interfere with the subject's participation in or
completion of the study

- Subject has a positive urine screen for prohibited drugs (cocaine, cannabinoids,
nicotine [urine cotinine is the detection mechanism for nicotine], opiates,
barbiturates, amphetamines, and benzodiazepines) or positive urine test for alcohol

- Subject has a positive blood screen for human immunodeficiency virus, hepatitis B
surface antigen, or hepatitis C virus antibody at the Screening Visit

- Subject has had a known or suspected hypersensitivity or idiosyncratic reaction to
the cellulose used in the placebo to be used in this study

- Subject has donated blood or any blood products within 3 months before Screening or
plans to donate blood during or within 3 months after study completion

- Subject consumes an excessive amount of caffeine daily, defined as > 4 cups of coffee
or equivalent per day. Subjects will abstain from caffeine consumption for 48 hours
before dosing and while confined to the CRU.

- Subject has consumed or will consume any concomitant therapy; prescription or
over-the-counter (OTC) medication; or nutritional, herbal, or vitamin supplements
other than contraceptives (eg, oral, systemic) and ibuprofen (only if needed, maximum
2.4 g/day) from 14 days or 5 half-lives (whichever is longer) before dosing and while
confined to the CRU

- For Part 2 only: Subject has consumed any food, juice, beverage, or medication
(prescription or non-prescription) containing acetaminophen, alcohol, avocado,
banana, caffeine, eggplant, kiwi fruit, nut (hickory nut, pecan, walnut), pineapple,
plum, or tomato products within 48 hours before CRU admission