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Proportion of subjects achieving T Cmax within the target criteria at end of study, safety set (N = 95)
| Proportion of subjects post‐treatment | ||
|---|---|---|
| T Cmax criteria | Secondary efficacy target | TLANDO |
| ≤ 1.5 × ULN* | ≥ 85% | 82% |
| Between 1.8 × and 2.5 × ULN* | ≤ 5% | 5% |
| >2.5 × ULN* | 0% | 0% |
ULN is 1080 ng/dl: 1.5 × ULN = 1620 ng/dl, 1.8 × ULN = 1944 ng/dl, and 2.5 × ULN = 2700 ng/dl.
