Study 1: Apararenone PK (single dose, effects of food, sex, age, and race; and multiple doses) and PD (multiple doses) |
Design |
Randomized, double‐blind, placebo‐controlled |
Subjects |
Healthy male volunteers (except part 2.1, which was conducted in women); all were Caucasian (except part 2.3, which was conducted in Blacks of African/Caribbean descent) |
Age |
18–55 years (except in part 2.2, which was conducted in subjects aged ≥65 years) |
Body weight |
Women ≥50 kg, men ≥60 kg |
Data collection |
PK, safety, tolerability, PD |
Apararenone doses |
Part 1 — single ascending doses of 3.75, 10, 20, 40, 80, 160, 320, and 640 mg (at each dose, n = 6 plus 2 matched placebo recipients; fasting state [part 1.1], then fed state [part 1.2]) |
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Part 2.1 — single dose of 20 mg (n = 6) or placebo (n = 2) in women aged 18–55 years |
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Part 2.2 — single dose of 20 mg (n = 6) or placebo (n = 2) in men aged ≥65 years |
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Part 2.3 — single dose of 20 mg (n = 6) or placebo (n = 2) in men of Black African/Caribbean origin |
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Part 3.1 — daily doses of 10, 20, or 40 mg/day (days 1–14) in men; at each dose, n = 8 plus 2 matched placebo recipients |
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Part 3.2 — loading dose of 320 mg (day 1), followed by 10 mg/day (days 2–14) in men; n = 8 plus 2 matched placebo recipients |
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Part 3.3 — loading dose of 320, 80, or 40 mg (day 1), followed by 20, 5, or 2.5 mg/day, respectively (days 2–14) (males; at each dose, n = 8 plus 2 matched placebo recipients) |