Relative Bioavailability of MN-166 (Ibudilast) in Extended Release Tablet vs. Intermediate-release Capsule in Healthy Volunteers

Exclusion Criteria

• •1. History of clinically significant drug allergy or anaphylaxis, including known hypersensitivity to Pinatos® or its components.
• •2. History of any condition(s) which might affect drug absorption, metabolism or excretion.
• •3. Clinical evidence or a history of clinically significant cardiovascular, respiratory, renal, hepatic, gastrointestinal, hematological, neurologic, or other chronic disease as judged by the Investigator.
• •4. History of severe psychiatric disease, especially major depression. Severe psychiatric disease is defined as treatment with an antidepressant medication or a major tranquilizer at therapeutic doses for major depression or psychosis, respectively, for at least 3 months at any previous time or any history of the following: a suicidal attempt, hospitalization for psychiatric disease, or a period of disability due to a psychiatric disease.
• •5. History of severe cardiac disease \[e.g., New York Heart Association (NYHA) Functional Class III or IV\], myocardial infarction within 6 months, ventricular tachyarrhythmias requiring ongoing treatment, unstable angina or other significant cardiovascular diseases.
• •6. Estimated creatinine clearance outside the normal range (\</= 80 mL/min) at screening.
• •7. History or other evidence of severe illness or any other conditions which would make the subject, in the opinion of the investigator, unsuitable for the study.
• •8. Evidence of alcohol and/or drug abuse within one year of screening.
• •9. Positive results on screen for drugs of abuse or alcohol at screening visit or Day 0.
• •10. History within 1 year of screening visit, or current habit, of smoking more than 10 cigarettes per day or equivalent (\>3 cigars or \>3 pipes-full).
• •11. Donated blood in the past 90 days or have poor peripheral venous access.
• •12. Platelets \< 100,000/mm3, history of thrombocytopenia.
• •13. Confirmed diagnosis of chronic liver disease, for example, chronic Hepatitis B, Hepatitis C infection, auto-immune, alcoholic or neoplastic liver disease.
• •14. Positive serostatus for HIV, HCV, or HBV.
• •15. Currently pregnant or nursing.
• •16. Male partners of females who are pregnant.
• •17. History of clinically significant cardiovascular, pulmonary, endocrine, neurological, metabolic, or psychiatric disease.
• •18. Participation in a clinical study with an investigational drug, biologic, or device within 3 months before receiving study drug.
• •19. Used any systemic medications, including vitamins and over-the-counter items, during the 14 days (or five times the elimination half-life of the medication, whichever is longer) before receiving study drug or will require their use during the study. Metabolic inducers and herbal preparations, which have been shown to produce metabolic enzyme induction or inhibition, whether as teas or formulations, are prohibited 28 days before dosing. Paracetamol 3000 mg/day will be allowed up to 2 consecutive days before dosing and during the outpatient phase of the study, as needed.
• •20. Unable to swallow large tablets.