The Effects of Rifampin on the Pharmacokinetics of Rosuvastatin
Status: | Active, not recruiting |
---|---|
Conditions: | Healthy Studies |
Therapuetic Areas: | Other |
Healthy: | No |
Age Range: | 18 - 65 |
Updated: | 4/21/2016 |
Start Date: | November 2014 |
End Date: | March 2016 |
The Effects of Single-Dose Rifampin on the Pharmacokinetics of Rosuvastatin in Healthy White and Asian Volunteers
The effect of transporter inhibition by rifampin on the pharmacokinetics of rosuvastatin
will be studied in clinical trial in White and Asian healthy volunteers.
will be studied in clinical trial in White and Asian healthy volunteers.
Inclusion Criteria:
- Healthy Asian volunteers of Han-Chinese/Japanese/Korean descent whose parents and
grandparents are Han-Chinese/ Japanese/ Korean.
- Healthy Caucasian volunteers of White/Caucasian/European-born descent whose parents
and grandparents are White/Caucasian/European.
- Male or female, ages 18-65 years old, with no current medical conditions or active
diagnoses as determined by the study doctor based on history, physical exam, and
laboratory evaluations.
- Subjects who take no other medications two weeks prior to the study and during the
time course of the study including prescription medications, over-the-counter
medications, dietary supplements, or drugs of abuse.
- Subjects with the following genotype: SLCO1B1*1a and ABCG2 421CC.
- Subjects able to maintain adequate birth control during the study independent of
hormonal contraceptive use.
- Subjects able to abstain from grapefruit, grapefruit juice, oranges, orange juice,
caffeinated beverages and/or alcoholic beverages from 7am the day before the study to
completion of that study day.
- Participants determined to have normal liver and kidney function as measured at
baseline
- BMI between 18.0 - 30 kg/m2
- Subjects capable of fasting from food and beverages at least 8 hours prior to
medication dosing.
- Be able to read, speak, and understand English.
- Subjects capable of providing informed consent and completing the requirements of the
study.
Exclusion Criteria:
- Subjects with active medical problems
- Subjects on chronic prescription or OTC medication that cannot be stopped 2 weeks
prior to and during the study.
- Subjects incapable of multiple blood draws (HCT < 30mg/dL)
- Subjects with a history of rhabdomyolysis
- Subjects with a history of drug-related myalgias
- Subjects with a history or diagnosis of hemorrhagic tendencies or blood dyscrasias
- Subjects with a history of GI bleed or peptic ulcer disease
- Subjects who smoke tobacco or have ongoing alcohol or illegal drug use
- Subjects who are pregnant, lactating, or trying to conceive during the study period
- Subjects allergic to rosuvastatin or rifampin or any known component of the
medications
- Anyone who in the opinion of the study investigators is unable to do the study
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