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Treatment-emergent adverse event (TEAEs) occurring at weeks 4, 8 and 12
| Week 4 | Week 8 | Week 12 | |
|---|---|---|---|
| Patients n | 60 | 58 | 53 |
| Patients with ≥ 1 TEAE | 1 (1.7%) | 2 (3.4%) | 3 (5.7%) |
| •Injection site erythema | 1 (1.7%) | 1 (1.7%) | 1 (1.9%) |
| •Dizziness | - | 1 (1.7%) | - |
| •Abdominal pain | - | - | 1 (1.9%) |
| •Neck pain and somnolence | - | - | 1 (1.0%) |
| Discontinuation due to TEAEs | - | - | - |
| Discontinuation due to ineffectiveness | - | - | - |
