Table 2 Summary of treatment-related adverse events.

From: Safety and tolerability of oral vorolanib for neovascular (wet) age-related macular degeneration: a phase I, open-label study

 

25 mg

(N = 16)

50 mg

(N = 16)

75 mg

(N = 8)

100 mg

(N = 1)

Elevated ALT

3 (18.8%)

9 (56.3%)

5 (62.5%)

0

Elevated AST

3 (18.8%)

8 (50.0%)

4 (50.0%)

0

Elevated blood pressure

4 (25.0%)

6 (37.5%)

3 (37.5%)

0

Leucopenia

1 (6.3%)

3 (18.8%)

3 (37.5%)

0

QT interval prolongation

2 (12.5%)

4 (25.0%)

1 (12.5%)

0

Thrombocytopenia

2 (12.5%)

1 (6.3%)

3 (37.5%)

0

Neutropenia

1 (6.3%)

3 (18.8%)

2 (25.0%)

0

Hair colour changes

0

4 (25.0%)

2 (25.0%)

0

  1. Data are number of participants (%). Treatment-related adverse events reported in ≥10% of all participants.
  2. ALT alanine aminotransferase, AST aspartate transaminase.