A Study to Investigate the Effect of Capivasertib on the Pharmacokinetics of Oral Rosuvastatin in Healthy Participants

Exclusion Criteria

• •1. History of any clinically important disease or disorder which may either put the participant at risk because of participation in the study or influence the results or the participant's ability to participate in the study.
• •2. History or presence of gastrointestinal, hepatic, or renal disease or any other condition known to interfere with absorption, distribution, metabolism, or excretion of drugs.
• •3. Any clinically important illness, medical/surgical procedure, or trauma.
• •4. Any clinically significant skin abnormalities that are chronic or currently active.
• •5. Any clinically important abnormalities in clinical chemistry, hematology, or urinalysis results.
• •6. Any positive result on screening for serum Hepatitis B surface antigen (HBsAg), Hepatitis B core antibody (HBcAb), Hepatitis C virus antibody (HCV antibody), or Human Immunodeficiency Virus (HIV).
• •7. Any clinically significant abnormalities in blood lipid profiles (triglycerides, high-density lipoprotein, low-density lipoprotein, and total cholesterol).
• •8. Any clinically significant abnormalities in glucose metabolism, including:
• •1. Diagnosis of type I or II diabetes mellitus (irrespective of management),
• •2. Fasting blood glucose ≥ 100 mg/dL, or
• •3. Hemoglobin A1c \> 5.7% after at least 8 hours of fasting at screening.
• •9. Any clinically significant abnormal findings in vital signs.
• •10. Any clinically significant abnormalities on 12-lead electrocardiogram (ECG) and defined as Sick sinus syndrome, arrhythmia, prolonged QTcF \> 450 ms, family history of long QT syndrome, persistent or intermittent bundle branch block, and atrio-ventricular block Grade II or III.
• •11. Current smokers or those who have smoked or used nicotine products (including e-cigarettes) within the previous 3 months.
• •12. Known or suspected history of alcohol or drug abuse or excessive intake of alcohol.
• •13. History of severe allergy/hypersensitivity or ongoing clinically important allergy/hypersensitivity or history of hypersensitivity to drugs with a similar chemical structure or class to capivasertib or rosuvastatin or history of hypersensitivity to any component of the finished dosage form of capivasertib.
• •14. Plasma donation or any blood donation/blood loss prior to the Screening Visit.
• •15. Participants who have previously received capivasertib.