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A Study to Evaluate the Effect of Mild or Moderate Hepatic Impairment on the Pharmacokinetics of Ozanimod - RPC-1063-CP-004

Actualizada: 17 noviembre, 2020   |   ClinicalTrials.gov

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Detalles del estudio

  • Phase 1

    Fase

  • Géneros

  • 18-75

    Rango de edad

  • Not Yet Recruiting

Opciones de tratamiento

Brazos del estudio
INTERVENCIÓN ASIGNADA
Experimental: Ozanimod in healthy subjects
Drug: Ozanimod
Experimental: Ozanimod in subjects with mild hepatic impairment
Drug: Ozanimod
Experimental: Ozanimod in subjects with moderate hepatic impairment
Drug: Ozanimod

Criterios clave de elegibilidad

Inclusion Criteria: Inclusion Criteria for all participants (Groups 1 through 3) Participants must satisfy the following criteria to be enrolled in the study: 1. Participant must understand and voluntarily sign an informed consent form (ICF) prior to any study-related assessments/procedures being conducted. 2. Participant is willing and able to adhere to the study visit schedule and other protocol requirements. 3. Participant is a male, or non-pregnant and non-lactating female ≥ 18 and ≤ 75 years of age at the time of signing the ICF. 4. Body weight of at least 110 pounds (50 kg); body mass index (BMI) ≥ 18.0 and ≤ 40.0 kg/m2, inclusive (Screening and Day -1). 5. Female Participants must meet at least 1 of the following criteria: - Negative serum pregnancy test at Screening and Day -1 (females of child-bearing potential [FCBP] only). - Postmenopausal at Screening. - Received surgical sterilization at least 6 months before Screening with medical records. 6. Females of child-bearing potential (FCBP) Must agree to practice a highly effective method of contraception throughout the study until 90 ± 10 days after the last dose. Inclusion Criteria for Participants with Mild or Moderate Hepatic Impairment (Groups 1 and 2) Each Participant with mild or moderate hepatic impairment must satisfy the following criteria to be enrolled in the study: 1. Participant has mild (5 to 6 points) or moderate (7 to 9 points) hepatic impairment per the Child-Pugh system. Participants should be enrolled into the group corresponding to the Child-Pugh classification score that most accurately reflects the most severe hepatic disease classification within the past 6 months (based on past medical history or PE observation). 2. Participant must be medically stable for at least 4 weeks before Screening with clinically acceptable medical history (eg, no worsening of clinical signs of hepatic impairment, or no worsening of total bilirubin or prothrombin time by more than 50%), PE, clinical laboratory tests, vital signs, and 12-lead ECGs consistent with the underlying stable hepatic impairment condition, as judged by the Investigator. 3. Participants with laboratory parameters that are considered clinically significant beyond those consistent with their degree of hepatic impairment may be included if, in the opinion of the Investigator and Medical Monitor, these findings will not interfere with the study or introduce additional safety risk to the Participant. 4. Participant must be stable on a concomitant medication and/or treatment regimen (defined as not starting a new treatment/medication[s] or a change in the dosage or frequency of the concomitant medication[s] within 2 weeks before dosing with ozanimod). 5. Participant must have estimated creatinine clearance ≥ 50 mL/min at Screening as calculated by the Cockcroft-Gault formula. Inclusion Criteria for Matched Normal Hepatic Function Participants (Group 3) Each matched Participant must satisfy the following criteria to be enrolled in the study: 1. Participant is in good health as determined by past medical history, PE, vital signs, ECG, and clinical laboratory safety tests. Clinical laboratory safety tests (ie, hematology, coagulation, chemistry, and urinalysis) must be within normal limits or clinically acceptable as judged by the Investigator. 2. Participant must match a Participant in Groups 1 and/or 2, with respect to sex, age (± 10 years), weight (± 20%) and smoking status. One normal hepatic function Participant can be matched to 2 hepatic impairment Participants (one in Group 1 and one in Group 2), but no more than one hepatic impairment Participant in the same group. Exclusion Criteria: The presence of any of the following will exclude a Participant from enrollment: 1. 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. 2. Participant has any condition that confounds the ability to interpret data from the study. 3. Participant has a seated blood pressure outside 90 to 155 mmHg systolic or 50 to 95 mmHg diastolic at Screening or Day -1. 4. Participant has a seated pulse rate outside 55 to 90 beats per minute (bpm) at Screening or Day -1. 5. Participant has a positive serum test for human immunodeficiency virus (HIV) at Screening or Day -1. 6. Participants with any active infection including hepatitis. 7. Participant has a positive alcohol urine or breath test at Screening or Day -1. 8. 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. 9. 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. 10. Participant fails or is unwilling to abstain from strenuous physical activities for at least 24 hours prior to the first dose of IP. 11. Participant has poor peripheral venous access. 12. Participant has donated greater than 400 mL of blood within 60 days prior to Day 1. 13. Participant has history of hypersensitivity or allergic reaction to S1P receptor modulators. 14. 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. 15. Participants who in the last 6 months experienced myocardial infarction, unstable angina, stroke, transient ischaemic attack, decompensated heart failure requiring hospitalization or New York Heart Association (NYHA) Class III/IV heart failure. 16. Participants 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. 17. Participants with history of cardiac arrest, cerebrovascular disease, uncontrolled hypertension, or severe untreated sleep apnoea, history of recurrent syncope or symptomatic bradycardia 18. Participants 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. 19. Participants 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. Exclusion Criteria for Participants with Hepatic Impairment (Groups 1 and 2) The presence of any of the following will exclude a hepatically-impaired Participant from enrollment: 1. 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. 2. 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. 3. 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. 4. Participant has a history of alcoholism, drug abuse, or addiction within 6 months prior to Screening. 5. 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. 6. Participant has any history of cholecystectomy, clinically significant cardiovascular or cerebrovascular disease. 7. Participant has severe ascites at Screening or Day -1. 8. Participant has hepatocellular carcinoma or acute liver disease (eg, caused by an infection or drug toxicity). 9. Participant chronically or routinely uses more than 2 g of acetaminophen daily. Exclusion Criteria for Matched Normal Hepatic Function Participants (Group 3) The presence of any of the following will exclude a matched normal hepatic function Participant from enrollment: 1. Participant has any significant medical condition or psychiatric illness that would prevent the Participant from participating in the study (as determined by the Investigator). 2. Participant has a history of alcoholism, drug abuse, or addition within 24 months prior to Screening. 3. Participant has a positive test result for hepatitis B surface antigen and/or hepatitis C antibody. 4. Participant has a positive urine drug test (except for cotinine in smokers) at Screening or Day -1. 5. 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.

Recomendamos encarecidamente que se comunique con BMS para informar los efectos secundarios (eventos adversos)
Los efectos secundarios (eventos adversos) y otros eventos reportables se definen aquí
Informe de efectos secundarios (eventos adversos) o quejas sobre la calidad del producto: información médica

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Llame 855-907-3286 o Envíenos un correo electrónico