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. 2021 Jun 21;14(6):2132–2138. doi: 10.1111/cts.13079

TABLE 1.

Summary of pharmacokinetic variables of daridorexant administered as single oral dose of 25 mg to control subjects (N = 7) and patients with SRFI (N = 8)

Control subjects

(Group A, N = 7) a

Patients with SRFI

(Group B, N = 8) a

Ratio of geometric means (90% CI), B/A b
Cmax, ng/ml 794 (445–1417) 744 (573–965) 0.94 (0.60–1.46)
T max, h 0.75 (0.50–3.00) 0.75 (0.50–1.50) −0.25 (−0.75–0.25)
AUC0‐t, ng·h/ml 5783 (2741–12,199) 7000 (5136–9541) 1.21 (0.69–2.12)
AUC0‐inf, ng·h/ml 6223 (2780–13,931) 7192 (5138–10,068) 1.16 (0.63–2.12)
t ½, h 11.4 (7.57–17.1) 11.2 (7.74–16.3) 0.99 (0.66–1.48)
CL/F, L/h 4.01 (1.79–8.99) 3.48 (2.48–4.87) 0.87 (0.47–1.59)
Vz/F, L 65.9 (43.8–99.1) 56.2 (49.1–64.3) 0.85 (0.64–1.15)

Abbreviations: AUC0‐inf, area under the plasma concentration‐time curve from zero to infinity; AUC0‐t, area under the plasma concentration‐time curve from zero to time t of the last measured concentration above the limit of quantification; CI, confidence interval; CL/F, apparent total plasma clearance; Cmax, maximum plasma concentration; SRFI, severe renal function impairment; t ½, terminal half‐life; T max, time to reach maximum plasma concentration; V z/F, apparent volume of distribution.

a

Data are presented as geometric mean (95% CI) except for T max: median (range).

b

Data are presented as geometric mean ratios (B/A; 90% CI) except for T max: median difference (B‐A; 90% CI).