Table 1. Serious adverse events and ocular treatment-emergent adverse events in the study eye.
| Adverse event n (%) of participants with events |
SAD | MAD | |||
|---|---|---|---|---|---|
| 0.5 mg (n=3) |
2 mg (n=3) |
4 mg (n=6) |
2 mg (n=6) |
4 mg (n=6) |
|
| Ocular SAE | 0 | 0 | 0 | 0 | 0 |
| Systemic SAE | 0 | 0 | 0 | 1 (16.7)* | 0 |
| Ocular TEAE in the study eye | 1 (33.3) | 0 | 1 (16.7) | 1 (16.7) | 2 (33.3) |
| IOP increased | 1 (33.3) | 0 | 0 | 0 | 0 |
| Conjunctival haemorrhage | 0 | 0 | 1 (16.7) | 0 | 0 |
| Allergic conjunctivitis | 0 | 0 | 0 | 1 (16.7) | 0 |
| Posterior capsular opacification | 0 | 0 | 0 | 0 | 1 (16.7) |
| Vision acuity decreased | 0 | 0 | 0 | 0 | 1 (16.7) |
IOP, intraocular pressure; MAD, multiple ascending dose; SAD, single ascending dose; SAE, serious adverse event; TEAE, treatment-emergent adverse event.