A Phase 1, Multicenter, Open-Label Study to Evaluate the Effect of Mild or Moderate Hepatic Impairment on the Multiple-Dose Pharmacokinetics of Ozanimod

Exclusion Criteria

• •The presence of any of the following will exclude a participant from enrollment:
• •Participant has any condition including the presence of laboratory abnormalities, which places the participant at unacceptable risk if he/she were to participate in the study.
• •Participant has any condition that confounds the ability to interpret data from the study.
• •Participant has a seated blood pressure outside 90 to 155 mmHg systolic or 50 to 95 mmHg diastolic at Screening or Day -1.
• •Participant has a seated pulse rate outside 55 to 90 beats per minute (bpm) at Screening or Day -1.
• •Participant has a positive serum test for human immunodeficiency virus (HIV) at Screening or Day -1.
• •Participant with any active infection including hepatitis.
• •Participant has a positive alcohol urine or breath test at Screening or Day -1.
• •Participant has received any investigational drug within 30 days or 5 times the elimination half-life (if known), whichever is longer, prior to the first dose of IP.
• •Participant has consumed pomelo-variety citrus fruits or juice (including pomelo, grapefruit, Seville oranges) within 7 days prior to the first dose of IP or herbal supplements including St. John's wort within 28 days prior to the first dose of IP.
• •Participant fails or is unwilling to abstain from strenuous physical activities for at least 24 hours prior to the first dose of IP.
• •Participant has poor peripheral venous access.
• •Participant has donated greater than 400 mL of blood within 60 days prior to Day 1.
• •Participant has history of hypersensitivity or allergic reaction to S1P receptor modulators.
• •Participant has used any of the following systemic medications:
• •1. Strong inhibitors of CYP3A, and all inhibitors of CYP2C8 or BCRP, (ie, cyclosporine, eltrombopag, gefitinib) within 7 days or 5 half-lives, whichever is longer, prior to Day 1, or
• •2. Strong inducers of CYP3A, and all inducers of CYP2C8 within 14 days or 5 halflives, whichever is longer, prior to Day 1, or
• •3. Any known MAO inhibitors within 30 days or 5 half-lives, whichever is longer, prior to Day 1. Examples of MAO inhibitors include but are not limited to phenelzine, selegiline, isocarboxazid, rasagiline, tranylcypromine, pargyline, procarbazine, and furazolidone.
• •Participant who in the last 6 months of signing the ICF experienced myocardial infarction, unstable angina, stroke, transient ischaemic attack, decompensated heart failure requiringmhospitalization or New York Heart Association (NYHA) Class III/IV heart failure.
• •Participant with history or presence of second-degree atrioventricular (AV) block Type II or third-degree AV block or sick sinus syndrome unless the patient has a functioning pacemaker.
• •Participant with history of cardiac arrest, cerebrovascular disease, uncontrolled hypertension, or severe untreated sleep apnoea, history of recurrent syncope or symptomatic bradycardia
• •Participant with pre-existing significant QT interval prolongation (QTc greater than 500 msec) or other risks for QT prolongation, and patients on medicinal products other than beta-blockers and calcium-channel blockers that may potentiate bradycardia.
• •Participant on class Ia (eg, quinidine, disopyramide) or class III (eg, amiodarone, sotalol) antiarrhythmic medicinal products, which have been associated with cases of torsades de pointes in patients with bradycardia have not been studied with ozanimod.
• •The presence of any of the following will exclude a hepatically-impaired participant from enrollment:
• •Participant has any serious medical condition (excluding hepatic impairment and related complications), clinically significant laboratory abnormality not related to hepatic impairment and related complications, or psychiatric illness that would prevent the participant from participating in the study per Investigator discretion.
• •Participant has current hepatic encephalopathy with time-or place-disorientation, somnolence, stupor, coma, no personality/behavior, rigidity, or hyperactive reflexes - or has had such within 1 month of Screening.
• •Participant has planned liver transplantation within 6 months of Screening or has received a liver transplant, transjugular intrahepatic portosystemic shunt, or transjugular intrahepatic portosystemic stent shunting procedure.
• •Participant has a history of alcoholism, drug abuse, or addiction within 6 months prior to Screening.
• •Participant has a positive urine drug screen including cotinine (non-smokers and former smokers only) (except for prescribed medications such as benzodiazepines) at Screening or Day -1. Tetrahydrocannabinol use (as permitted by local law) is not allowed within 14 days prior to Day 1 and during the study.
• •Participant has any history of cholecystectomy, clinically significant cardiovascular or cerebrovascular disease.
• •Participant has severe ascites at Screening or Day -1.
• •Participant has hepatocellular carcinoma or acute liver disease (eg, caused by an infection or drug toxicity).
• •Participant chronically or routinely uses more than 2 g of acetaminophen daily.
• •The presence of any of the following will exclude a matched normal hepatic function participant from enrollment:
• •Participant has any significant medical condition or psychiatric illness that would prevent the participant from participating in the study (as determined by the Investigator).
• •Participant has a history of alcoholism, drug abuse, or addition within 24 months prior to Screening.
• •Participant has a positive test result for hepatitis B surface antigen and/or hepatitis C antibody.
• •Participant has a positive urine drug test (except for cotinine in smokers) at Screening or Day -1.
• •Participant has used any systemic over-the-counter medication (excluding acetaminophen up to 2 g/day and low dose aspirin) within 7 days prior to Day 1, or any systemic prescription medication (except for contraceptives) within 28 days or 5-half-lives, whichever is longer, prior to Day 1.