Cohort1: AGN 211745_dose level 1
|
Administration route |
None |
Dosage |
AGN 211745 Solution, 1000µg, at Day 1, Month 1, Month 2 |
Pts |
34 |
Age |
Adult, Older_Adult |
Outcome |
Percentage of Patients With Improvement in Best Corrected Visual Acuity (BCVA) of 15 or More Letters at Month 3:Measure Type: Number:5.9 |
Adverse reactions |
4/34(Neoplasms benign, malignant and unspecified(incl cysts and polyps); Vascular disorders) |
|
Cohort2: AGN 211745_dose level 2
|
Administration route |
None |
Dosage |
AGN 211745 Solution, 300µg, at Day 1, Month 1, Month 2 |
Pts |
35 |
Age |
Adult, Older_Adult |
Outcome |
Percentage of Patients With Improvement in Best Corrected Visual Acuity (BCVA) of 15 or More Letters at Month 3:Measure Type: Number:2.9 |
Adverse reactions |
3/35(Cardiac disorders; Nervous system disorders; Reproductive system and breast disorders) |
|
Cohort3: AGN 211745_dose level 3
|
Administration route |
None |
Dosage |
AGN 211745 Solution, 100µg, at Day 1, Month 1, Month 2 |
Pts |
35 |
Age |
Adult, Older_Adult |
Outcome |
Percentage of Patients With Improvement in Best Corrected Visual Acuity (BCVA) of 15 or More Letters at Month 3:Measure Type: Number:0 |
Adverse reactions |
3/35(Gastrointestinal disorders; Infections and infestations) |
|
Cohort4: Ranibizumab
|
Administration route |
None |
Dosage |
Ranibizumab, 500µg, at Day 1, Month 1, Month 2 |
Pts |
34 |
Age |
Adult, Older_Adult |
Outcome |
Percentage of Patients With Improvement in Best Corrected Visual Acuity (BCVA) of 15 or More Letters at Month 3:Measure Type: Number:17.6 |
Adverse reactions |
9/34(Cardiac disorders; Hepatobiliary disorders; Infections and infestations; Metabolism and nutrition disorders; Neoplasms benign, malignant and unspecified(incl cysts and polyps); Vascular disorders) |
|