Cohort1: SYL040012_dose level 1
|
Administration route |
drop |
Dosage |
SYL040012, 0.375%, each eye once daily |
Pts |
37 |
Age |
Adult, Older_Adult |
Outcome |
Change From Baseline in the Mean Diurnal IOP:-2.4 |
Adverse reactions |
No serious clinical adverse events |
|
Cohort2: SYL040012_dose level 2
|
Administration route |
drop |
Dosage |
SYL040012, 0.750%, each eye once daily |
Pts |
40 |
Age |
Adult, Older_Adult |
Outcome |
Change From Baseline in the Mean Diurnal IOP:-3.2 |
Adverse reactions |
No serious clinical adverse events |
|
Cohort3: SYL040012_dose level 3
|
Administration route |
drop |
Dosage |
SYL040012, 1.125%, each eye once daily |
Pts |
37 |
Age |
Adult, Older_Adult |
Outcome |
Change From Baseline in the Mean Diurnal IOP:-3.1 |
Adverse reactions |
No serious clinical adverse events |
|
Cohort4: SYL040012_dose level 4
|
Administration route |
drop |
Dosage |
SYL040012, 1.5%, each eye once daily |
Pts |
33 |
Age |
Adult, Older_Adult |
Outcome |
Change From Baseline in the Mean Diurnal IOP:-3.1 |
Adverse reactions |
No serious clinical adverse events |
|
Cohort5: Timolol maleate
|
Administration route |
drop |
Dosage |
Timolol maleate, 0.5%, each eye once daily |
Pts |
37 |
Age |
Adult, Older_Adult |
Outcome |
Change From Baseline in the Mean Diurnal IOP:-6.1 |
Adverse reactions |
No serious clinical adverse events |
|