Table 1.
Open-label baseline | |
Patients recruited from SPD489-325 in Europe (n = 222) | Visit 0 (week 0) of SPD489-325 (after screening and washout as part of SPD489-325) |
Additional US patients (n = 40) | Visit 1 (week 0) of the present study (after screening and washout as part of the present study) |
Open-label endpoint | |
Patients under the original protocol | The last on-treatment visit with valid data, up to and including visit 17 (week 52), or early termination |
Patients who switched protocols | The last on-treatment visit with valid data, up to and including visit 3R (week ≥26), or early termination |
Patients under the revised protocol | The last on-treatment visit with valid data, up to and including visit 3R (week 26), or early termination |
Randomized-withdrawal baseline | Visit 3R (week 0 of the randomized-withdrawal period) |
Randomized-withdrawal endpoint | Visit 9R (week 6 of the randomized-withdrawal period) or early termination |
See Fig. 1 for schedule of study visits. Numbers are those in the full analysis set. SPD489-325 was the previous 7-week, European, phase III study of LDX
R revised