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. 2024 Jan 25;68:102433. doi: 10.1016/j.eclinm.2024.102433

Table 3.

Treatment-emergent adverse events.

Safety event S48168 (ARM210) dose group
120 mg/day (N = 3)
200 mg/day (N = 4)
Events
Participants
Events
Participants
N N N N
Total treatment-emergent adverse events 17 3 9 3
Treatment-emergent adverse events ≥ grade two in severitya 2 2 1 1
Treatment-emergent adverse events at least possibly related to S48168 (ARM210) 2 2 0 0
Adverse events of special interest 0 0 0 0
Serious adverse events 0 0 0 0
Deaths 0 0 0 0
a

Defined per NCI Common Terminology Criteria for Adverse Events (version 5.0).