Identification and Validation of Biomarkers for Breast Cancer Resistance Protein (BCRP)

Open to people ages 18-64

• Healthy as judged by medical examination, medical history and normal biochemical and hematological measures.
• Normal urinalysis and renal function
• Male subjects weighing ≥ 50 kg and female subjects weighing ≥ 45 kg.
• Understand the nature and purpose of the study and provide informed consent.

• Subjects who are pregnant, breastfeeding, or unwilling to practice non-hormonal forms of birth control during participation in the study.
• Self-reported drug allergies to rosuvastatin or eltrombopag
• Subjects that have smoked cigarettes, have smoked or ingested THC/marijuana or have used illegal substances (i.e., opiates, cocaine) in the past year.
• Subjects with any disease affecting or impairing the function of the liver, kidney or heart.
• Subjects with any blood or coagulation disorders.
• Subjects with diabetes mellitus, hyperthyroidism, hypothyroidism, cardiovascular disease, glaucoma.
• Subjects with gastrointestinal disease, gastrointestinal disorder, or gastrointestinal surgery.
• Subjects with known infection with HIV, Hepatitis B (HBsAg) or Hepatitis C (no laboratory diagnostics concerning these diseases will be performed within the present study).
• Subjects that are taking prescription (i.e., birth control pills), non-prescription and dietary supplements (i.e., turmeric, quercetin, kaempferol, Gingko biloba) within seven days of receiving the study dose in each phase of the study.
• Subjects with a condition, disease, or abnormality that in the opinion of the Investigator would compromise the safety of the patient or the quality of the data.
• Female subjects undergoing treatment for infertility or hormone replacement therapy.
• Subjects with abnormal laboratory results at screening as judged by the investigator or study physician.
• Participating in another research study while participating in this research study.
• Subjects that ingest grapefruit, grapefruit juice or grapefruit extract within seven days of receiving the study dose in each phase of the study.
• Non-English speaking.
• Subject has any signs or symptoms that are consistent with COVID-19. Per current CDC recommendations this includes subjects with the symptoms cough or shortness of breath or difficulty breathing, or at least two of the following symptoms: fever, chills, repeated shaking with chills, muscle pain, headache, sore throat or new loss of taste/smell. In addition, the subject has any other findings suggestive of COVID-19 risk in the opinion of the investigator.
• Subject tests positive for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by a molecular diagnostic test (i.e., COVID19 RNA test) performed during the screening visit.