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. 2023 Jan 12;11(1):e006136. doi: 10.1136/jitc-2022-006136

Table 2.

Treatment-related AEs (≥ 3 participants)*

Event type 25 mg/240 mg†
N=55
Nausea 14 (25.5) [19]
Fatigue 12 (21.8) [17]
Diarrhea 10 (18.2) [16]
Decreased appetite 8 (14.5) [9]
Pyrexia 7 (12.7) [8]
Pruritus 6 (10.9) [6]
Alanine aminotransferase increased 5 (9.1) [6]
Aspartate aminotransferase increased 4 (7.3) [6]
Chills 3 (5.5) [3]
Pneumonitis 3 (5.5) [3]

*50 mg pixatimod/240 mg nivolumab data not presented as only three participants were recruited.

†For any given AE, the results are presented as the number of participants with the event: n, the proportion of participants with the event: (%), and the number of events: [e].

AEs, adverse events.