Evaluate the Effect of Ethinyl Estradiol/Norgestimate on the Pharmacokinetics of Lomitapide in Healthy Female Subjects

Exclusion Criteria

• •1. significant history or clinical manifestation of any metabolic, allergic, dermatological, hepatic, renal, hematological, pulmonary, cardiovascular, GI, neurological, or psychiatric disorder
• •2. history of unexplained breast abnormalities or abnormal uterine bleeding
• •3. history of significant hypersensitivity, intolerance, or allergy to any drug compound, food, or other substance
• •4. history of stomach or intestinal surgery or resection
• •5. history of Gilbert's Syndrome or suspicion of Gilbert's Syndrome
• •6. subjects who have an abnormality in the 12-lead ECG
• •7. use of any drugs of abuse for 6 months prior to Check-in;
• •8. subjects who consume more than 14 units of alcohol per week or who have a significant history of alcoholism or drug/chemical abuse within 1 year prior to Check-in
• •9. use of any tobacco- or nicotine-containing products within 6 months prior to Check-in;
• •10. participation in any other investigational study drug trial within 30 days prior to Check-in;
• •11. use of any prescription medications/products within 14 days prior to Check-in unless deemed acceptable by the Investigator and Sponsor
• •12. use of any over-the-counter, nonprescription preparations within 7 days prior to Check-in, unless deemed acceptable by the Investigator and Sponsor
• •13. use of alcohol-, grapefruit- (including star fruit), or caffeine-containing foods or beverages within 72 hours prior to Check-in and through Study Completion
• •14. use of oral (except scheduled administration of EE/norgestimate), implantable, injectable, or transdermal contraceptives
• •15. use of hormone replacement therapy
• •16. poor peripheral venous access;
• •17. donation of blood (500 mL) from 30 days prior to Screening through Study Completion
• •18. receipt of blood products within 2 months prior to Check-in;
• •19. any acute or chronic condition, scheduled hospitalization (inclusive of elective surgery during study) or scheduled travel prior to completion of all study procedures which, in the opinion of the Investigator, would limit the subject's ability to complete and/or participate in this clinical study;
• •20. subjects who, in the opinion of the Investigator, should not participate in this study.