TABLE 2.
Parameter | NONMEM | Bootstrap | |
---|---|---|---|
Estimate | %RSE | Median (95% CI) | |
PD parameters | |||
Baseline SUVr | 1.34 | 0.873 | 1.34 (1.31–1.38) |
K in (1/year) | 0.232 | 11.1 | 0.232 (0.174–0.277) |
E max | 1.54 | 11.8 | 1.56 (1.10–2.01) |
EC50 (μg/ml) | 75.0 | 19.6 | 77.1 (38.5–121) |
Covariate | |||
APOE4 carrier ~ baseline | 1.04 | 1.04 | 1.04 (1.02–1.07) |
Age ~ E max (exponent) | 1.58 | 20.9 | 1.60 (0.972–2.07) |
Interindividual variability (CV%) | |||
Baseline | 10.9 | 8.12 | 11.0 (9.79–11.9) |
Correlation baseline ~ E max (R) | 0.669 | 11.5 | 0.674 (0.556–0.713) |
E max | 50.3 | 12.0 | 50.8 (42.1–59.7) |
Residual variability (CV%) | |||
Proportional | 5.01 | 2.75 | 5.02 (4.48–5.59) |
Abbreviations: %RSE, percent relative standard error of the estimate = SE/parameter estimate × 100; CI, confidence interval; CV%, square root of variance × 100; EC50, lecanemab concentration at which 50% of maximum drug effect is achieved; E max, maximum drug effect; K in, rate of production; PD, pharmacodynamic; PET, positron emission tomography; PK, pharmacokinetic; SUVr, standard uptake ratio.
.
AGE = age; APOE = 0 (APOE4 carrier) or 1 (non‐carrier).
Eta shrinkage (%): ETA_Baseline = 6.94%, ETA_E max = 27.7%.