Table 3.
Primary efficacy endpoint by periorbital indication. Proportion of ‘improved’ or ‘much improved’ GAIS scores for periorbital indications as assessed by both investigator and subject
| Main analysis (month 3 GAIS score, n = 157) | Sensitivity analysis (GAIS score at 29-153 days post-treatment or directly post-injection, n = 244) | ||||
|---|---|---|---|---|---|
| Indication | Sample size | ‘Improved’ or ‘much improved’ (n, %) | Indication | Sample size | ‘Improved’ or ‘much improved’ (n, %) |
| Tear trough | 53 | 41 (77.4%) | Tear trough | 89 | 75 (84.3%) |
| Palpebromalar groove | 43 | 31 (72.1%) | Palpebromalar groove | 61 | 47 (77.0%) |
| Crow’s feet | 24 | 17 (70.8%) | Crow’s feet | 38 | 31 (81.6%) |
| Outer canthus | 25 | 18 (72.0%) | Outer canthus | 37 | 29 (78.4%) |
| Brow | 12 | 8 (66.7%) | Brow | 19 | 15 (78.9%) |