Safety, Tolerability, and Pharmacokinetics of a Single Oral Dose of SKI-O-703 in Healthy Volunteers

Exclusion Criteria

• •History of any clinically significant disease or disorder that may put the subject at risk if he/she participates in the study, might affect the subject's ability to participate in the study, or influence the study results
• •History or presence of any gastrointestinal, hepatic or renal disease, or any other condition known to interfere with the absorption, distribution, metabolism, or excretion (ADME) of drugs
• •Any surgical or medical conditions possibly affecting drug ADME (eg, bariatric procedure)
• •Any medical/surgical procedure or trauma within 4 weeks of Day -1 as determined by the investigator
• •Any clinically significant infection within 3 months of Day -1 as determined by the investigator
• •Any of the following abnormal laboratory values upon repeat testing at Screening or check-in:
• •* Hemoglobin \<the lower limit of normal (LLN)
• •* Platelet count \<LLN
• •* Absolute neutrophil count \<LLN or \>the upper limit of normal (ULN)
• •* Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) \>ULN
• •* Creatinine or blood urea nitrogen \>ULN
• •* Other clinically significant abnormal laboratory results in the opinion of the investigator
• •Use of concomitant medications from 30 days or 5 half-lives prior to Day -1 (whichever is longer), including prescription medications, nutritional supplements, herbal remedies, and over-the-counter medications
• •Receipt of any investigational medication within 30 days or 5 half-lives prior to Day -1, whichever is longer
• •Use of tobacco or nicotine-containing products within 30 days prior to Day -1 and through the End-of-Study visit
• •Use of cytochrome P450 3A isozyme (CYP3A) inducers and inhibitors (including St. John's wort) within 30 days of dosing
• •Food or beverage containing alcohol, grapefruit or grapefruit juice, apple or orange juice, vegetables from the mustard green family (eg, kale, broccoli, watercress, collard greens, kohlrabi, brussels sprouts, mustard), and charbroiled meats within 1 week prior to dosing
• •History of substance abuse, drug addiction, or alcoholism
• •Positive urine drug or urine alcohol test result at screening or Day -1 or unable to abstain from alcohol from 72 hours prior to study entry to the End-of-Study visit
• •Unable to abstain from caffeine and xanthine-containing products from 72 hours prior to dosing through discharge from the study site
• •Female subjects who are pregnant or lactating or have a positive serum pregnancy test result at Screening
• •Positive test results at Screening for human immunodeficiency virus, hepatitis B surface antigen (HBsAg), hepatitis C virus antibody, or hepatitis B core antibody and negative for HBsAg
• •Recent (past 5 years) history of malignancy except successfully treated basal cell carcinoma
• •High blood pressure, defined as \>140 millimeters of mercury (mm Hg) systolic blood pressure or \>90 mm Hg diastolic blood pressure upon repeat confirmation
• •Cardiac arrhythmias or clinically significant ECG findings upon repeat confirmation by the investigator
• •Corrected QT interval (QTc) \>450 milliseconds or deemed clinically significant by the investigator
• •Family history of long QT syndrome
• •Blood loss or blood donation \>450 mL within 4 weeks of study drug dosing
• •History of sensitivity to drugs with chemical similarity to the study drug, its components, or excipients