4.1 Mean IOP changes from baseline |
4 |
|
Mean Difference (IV, Random, 95% CI) |
Subtotals only |
4.1.1 Netarsudil 0.02% + latanoprost 0.005% (FDC) once per day vs latanoprost 0.005% once per day |
3 |
1114 |
Mean Difference (IV, Random, 95% CI) |
‐1.64 [‐2.16, ‐1.11] |
4.1.2 Ripasudil 0.4% twice per day + latanoprost 0.005% once per day vs latanoprost 0.005% once per day |
1 |
205 |
Mean Difference (IV, Random, 95% CI) |
‐0.29 [‐0.86, 0.28] |
4.2 Total ocular adverse events (per person‐month) – incidence rate difference |
4 |
|
Risk Difference (IV, Random, 95% CI) |
0.26 [0.13, 0.40] |
4.2.1 Netarsudil 0.02% + latanoprost 0.005% (FDC) once per day vs latanoprost 0.005% once per day |
3 |
|
Risk Difference (IV, Random, 95% CI) |
0.29 [0.11, 0.47] |
4.2.2 Ripasudil 0.4% twice per day + latanoprost 0.005% once per day vs latanoprost 0.005% once per day |
1 |
|
Risk Difference (IV, Random, 95% CI) |
0.21 [0.11, 0.31] |
4.3 Conjunctival hyperemia as adverse event (per person‐month)* |
4 |
|
Risk Difference (IV, Random, 95% CI) |
0.15 [0.03, 0.27] |
4.3.1 Netarsudil 0.02% + latanoprost 0.005% (FDC) once per day vs latanoprost 0.005% once per day |
3 |
|
Risk Difference (IV, Random, 95% CI) |
0.10 [0.00, 0.20] |
4.3.2 Ripasudil 0.4% twice per day + latanoprost 0.005% once per day vs latanoprost 0.005% once per day |
1 |
|
Risk Difference (IV, Random, 95% CI) |
0.24 [0.16, 0.32] |
4.4 Ocular pain or irritation as adverse event (per person‐month)* |
4 |
|
Risk Difference (IV, Random, 95% CI) |
0.03 [‐0.00, 0.07] |
4.4.1 Netarsudil 0.02% + latanoprost 0.005% (FDC) once per day vs latanoprost 0.005% once per day |
3 |
|
Risk Difference (IV, Random, 95% CI) |
0.05 [0.01, 0.09] |
4.4.2 Ripasudil 0.4% twice per day + latanoprost 0.005% once per day vs latanoprost 0.005% once per day |
1 |
|
Risk Difference (IV, Random, 95% CI) |
‐0.02 [‐0.06, 0.02] |