Table 1.

Treatment exposure, dose intensity, dose adjustment, and study drug discontinuation

Dosing and exposureMomelotinib overall (N = 725)Momelotinib-randomized treatment phase (n = 448)Momelotinib open-label phase (n = 604)
Median duration of exposure (range), mo 11.3 (0.1-90.4) 5.5 (0.1-6.1) 11.0 (0.0-85.0) 
Duration of exposure, n (%)    
≥4 wk 684 (94.3) 425 (94.9) 565 (93.5) 
≥8 wk 637 (87.9) 402 (89.7) 515 (85.3) 
≥12 wk 602 (83.0) 385 (85.9) 486 (80.5) 
≥24 wk 513 (70.8) 207 (46.2) 406 (67.2) 
≥48 wk 367 (50.6) — 302 (50.0) 
≥96 wk 213 (29.4) — 193 (32.0) 
≥36 mo 134 (18.5) — 122 (20.2) 
≥48 mo 103 (14.2) — 98 (16.2) 
≥60 mo 88 (12.1) — 84 (13.9) 
Average daily dose, median (range), mg 194.6 (0-494) 200.0 (0-229) 194.3 (0-775) 
Relative dose intensity, median (range), % 97.3 (0-247) 100 (0-114) 97.2 (0-387) 
Dosing and exposureMomelotinib overall (N = 725)Momelotinib-randomized treatment phase (n = 448)Momelotinib open-label phase (n = 604)
Median duration of exposure (range), mo 11.3 (0.1-90.4) 5.5 (0.1-6.1) 11.0 (0.0-85.0) 
Duration of exposure, n (%)    
≥4 wk 684 (94.3) 425 (94.9) 565 (93.5) 
≥8 wk 637 (87.9) 402 (89.7) 515 (85.3) 
≥12 wk 602 (83.0) 385 (85.9) 486 (80.5) 
≥24 wk 513 (70.8) 207 (46.2) 406 (67.2) 
≥48 wk 367 (50.6) — 302 (50.0) 
≥96 wk 213 (29.4) — 193 (32.0) 
≥36 mo 134 (18.5) — 122 (20.2) 
≥48 mo 103 (14.2) — 98 (16.2) 
≥60 mo 88 (12.1) — 84 (13.9) 
Average daily dose, median (range), mg 194.6 (0-494) 200.0 (0-229) 194.3 (0-775) 
Relative dose intensity, median (range), % 97.3 (0-247) 100 (0-114) 97.2 (0-387) 
DiscontinuationsMomelotinib overall (N = 725)
Momelotinib discontinuation, n (%) 537 (74.1) 
Primary reason for momelotinib discontinuation  
AE 183 (25.2) 
Disease progression 100 (13.8) 
Insufficient treatment efficacy 63 (8.7) 
Patient decision 61 (8.4) 
Death 55 (7.6) 
Investigator discretion 47 (6.5) 
Study terminated by sponsor 18 (2.5) 
DiscontinuationsMomelotinib overall (N = 725)
Momelotinib discontinuation, n (%) 537 (74.1) 
Primary reason for momelotinib discontinuation  
AE 183 (25.2) 
Disease progression 100 (13.8) 
Insufficient treatment efficacy 63 (8.7) 
Patient decision 61 (8.4) 
Death 55 (7.6) 
Investigator discretion 47 (6.5) 
Study terminated by sponsor 18 (2.5) 

Data cutoff: 3 December 2021.

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