Primary-outcome results across pivotal trials
Per-arm reported values from Phase 2/3 and Phase 3 trials with results posted to ClinicalTrials.gov.
| Trial | Indication | Primary endpoint | Arm | Value |
|---|---|---|---|---|
| NCT00242580 VERITAS | Macular Degeneration | Percentage of Participants Who Lose Less Than 15 Letters of Best Corrected Visual Acuity (BCVA) at 12 Months From Baseline. Baseline to Month 12 | Verteporfin + 1 mg Triamcinolone | 59.4 Percentage of Participants |
| Verteporfin + 4 mg Triamcinolone | 63.4 Percentage of Participants | |||
| Verteporfin + Pegaptanib | 71.1 Percentage of Participants | |||
| NCT00433017 | Macular Degeneration | Change From Baseline in Best-corrected Visual Acuity (BCVA) at Month 12. Baseline and Month 12 | Ranibizumab | 4.4 Letters (±15.92 Standard Deviation) |
| Ranibizumab | 55.1 Letters (±12.3 Standard Deviation) | |||
| Ranibizumab | 59.4 Letters (±18.8 Standard Deviation) | |||
| Verteporfin + Ranibizumab | 54.6 Letters (±13.5 Standard Deviation) | |||
| Verteporfin + Ranibizumab | 2.5 Letters (±14.82 Standard Deviation) | |||
| Verteporfin + Ranibizumab | 57.1 Letters (±18.3 Standard Deviation) | |||
| NCT00433017 | Macular Degeneration | Percent of Participants With a Treatment-free Interval of at Least 3 Months Following the Month 2 Visit Month 2 to Month 11 | Ranibizumab | 92.2 Percentage of Participants |
| Verteporfin + Ranibizumab | 95.8 Percentage of Participants | |||
| NCT00436553 | Macular Degeneration | Mean Change From Baseline in Best-corrected Visual Acuity (BCVA) of the Study Eye at Month 12 Baseline and Month 12 | Ranibizumab Monotherapy | 63.0 Letters (±18.88 Standard Deviation) |
| Ranibizumab Monotherapy | 8.1 Letters (±15.09 Standard Deviation) | |||
| Ranibizumab Monotherapy | 54.8 Letters (±13.55 Standard Deviation) | |||
| Verteporfin RF + Ranibizumab | 4.4 Letters (±15.47 Standard Deviation) | |||
| Verteporfin RF + Ranibizumab | 59.0 Letters (±18.03 Standard Deviation) | |||
| Verteporfin RF + Ranibizumab | 54.6 Letters (±12.78 Standard Deviation) | |||
| Verteporfin SF + Ranibizumab | 5.3 Letters (±15.66 Standard Deviation) | |||
| Verteporfin SF + Ranibizumab | 53.7 Letters (±13.52 Standard Deviation) | |||
| Verteporfin SF + Ranibizumab | 59.0 Letters (±17.47 Standard Deviation) | |||
| NCT00436553 | Macular Degeneration | Percent of Patients With a Treatment-free Interval of at Least 3 Months Following the Month 2 Visit Month 2 up to Month 11 | Verteporfin RF + Ranibizumab | 83.5 Percent of participants |
| Verteporfin SF + Ranibizumab | 92.6 Percent of participants | |||
| NCT01217944 | Choroidal Neovascularization | Average Change From Baseline to Month 1 Through Month 3 on Visual Acuity of the Study Eye Baseline, Month 1 through Month 3 | 0.5 mg Ranibizumab Driven by Stabilization Criteria | 55.4 Letters (±13.43 Standard Deviation) |
| 0.5 mg Ranibizumab Driven by Stabilization Criteria | 66.0 Letters (±12.98 Standard Deviation) | |||
| 0.5mg Ranibizumab Driven by Disease Activity | 66.4 Letters (±12.28 Standard Deviation) | |||
| 0.5mg Ranibizumab Driven by Disease Activity | 55.8 Letters (±12.59 Standard Deviation) | |||
| Verteporfin PDT | 56.9 Letters (±14.49 Standard Deviation) | |||
| Verteporfin PDT | 54.7 Letters (±13.84 Standard Deviation) | |||
| NCT01922102 Brilliance | Choroidal Neovascularization | Change From Baseline BCVA to the Average Level of BCVA Over All Monthly Assessments From Month 1 to Month 3 From Baseline to Month 3 | Group I | 53.7 ETDRS letters (±12.65 Standard Deviation) |
| Group I | 63.1 ETDRS letters (±12.80 Standard Deviation) | |||
| Group II | 54.2 ETDRS letters (±13.01 Standard Deviation) | |||
| Group II | 63.9 ETDRS letters (±13.28 Standard Deviation) | |||
| Group III | 52.6 ETDRS letters (±12.29 Standard Deviation) | |||
| Group III | 57.1 ETDRS letters (±13.21 Standard Deviation) |