TABLE 1.
Summary of the simulation scenarios in this manuscript.
| (I) Simulation scenarios for specific populations with dosage regimen A | |||
|---|---|---|---|
| Caucasian healthy population (20–50 years) | |||
| Chinese healthy population (20–50 years) | |||
| Sim-cirrhosis CP-A populations (20–50 and 65–70 years) | |||
| Sim-cirrhosis CP-B populations (20–50 and 65–70 years) | |||
| Sim-cirrhosis CP-C populations (20–50 and 65–70 years) | |||
| Sim-renal-GFR-30–60 populations (20–50, 65–75 and 75–85 years) | |||
| Sim-renal-GFR-less-30 populations (20–50, 65–75 and 75–85 years) | |||
| Paediatric populations (0–0.5, 0.5–2, 2–6, 6–12, 12–17 years) | |||
| Pregnant population (13, 25, 37 gestational weeks) | |||
| Geriatric populations (65–75, 75–85, and 85–95 years) | |||
| (II) Simulation scenarios of potential drug drug interactions | |||
| Inhibitor | Treatment (days) | Dose regimen | HCQ dosage regimen (treatment) |
| Gemfibrozil (strong CYP2C8 inhibitor) | 12 | 600 mg BID | Regimen A (D 3 - D 7) |
| Quinidine (strong CYP2D6 inhibitor) | 12 | 200 mg QD | Regimen A (D 3 - D 7) |
| ritonavir (strong CYP3A4 inhibitor and weak CYP2D6 inhibitor) | 12 | 100 mg QD | Regimen A (D 3 - D 7) |