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