Table 2.
AEs, n (%) | Ecnoglutide | Placebo N = 36 | ||
---|---|---|---|---|
0.4 mg N = 37 | 0.8 mg N = 36 | 1.2 mg N = 36 | ||
All AE | 29 (78.4) | 28 (77.8) | 26 (72.2) | 22 (61.1) |
All TRAE | 18 (48.6) | 16 (44.4) | 16 (44.4) | 6 (16.7) |
TEAE ≥Grade 3 | 2 (5.4) | 0 | 2 (5.6) | 3 (8.3) |
TRAE ≥Grade 3 | 0 | 0 | 0 | 0 |
All AESI | 14 (37.8) | 13 (36.1) | 17 (47.2) | 6 (16.7) |
Treatment-related AESI | 14 (37.8) | 12 (33.3) | 15 (41.7) | 2 (5.6) |
TEAE leading to drug discontinuation | 0 | 0 | 1 (2.8) | 0 |
TRAE leading to drug discontinuation | 0 | 0 | 1 (2.8) | 0 |
All SAE | 0 | 0 | 1 (2.8) | 0 |
Treatment-related SAE | 0 | 0 | 0 | 0 |
TEAE leading to study withdrawal | 0 | 0 | 2 (5.6) | 0 |
TRAE leading to study withdrawal | 0 | 0 | 1 (2.8) | 0 |
TEAE leading to death | 0 | 0 | 0 | 0 |
TRAE leading to death | 0 | 0 | 0 | 0 |
AE adverse event, TRAE treatment-related AE, TEAE treatment-emergent AE, AESI adverse events of special interest, SAE serious adverse event.