Table 2.
Summary of AEs
| AE category | Oleclumab 1500 mg (n = 3) |
Oleclumab 3000 mg (n = 3) |
Total (N = 6) |
|---|---|---|---|
| Any AE | 3 (100.0) | 3 (100.0) | 6 (100.0) |
| Any AE related to treatment | 3 (100.0) | 2 (66.7) | 5 (83.3) |
| Any AE of CTCAE ≥ Grade 3 | 0 | 1 (33.3) | 1 (16.7) |
| Any AE of CTCAE ≥ Grade 3, related to treatment | 0 | 0 | 0 |
| Any AE with an outcome of death | 0 | 0 | 0 |
| Any AE with an outcome of death, related to treatment | 0 | 0 | 0 |
| System Organ Class/Preferred Term | |||
| Patients with AE of CTCAE Grade ≥ 3 | 0 | 1 (33.3) | 1 (16.7) |
| Investigations | 0 | 1 (33.3) | 1 (16.7) |
| Neutrophil count decreased | 0 | 1 (33.3) | 1 (16.7) |
All data are presented as n (%)
AE adverse event; CTCAE Common Terminology Criteria for Adverse Events