Clinical trial
Efficacy and Safety of RTH258 Versus Aflibercept - Study 1
NCT02307682 · Alcon Research, Industry · Completed
Key facts
| NCT number | NCT02307682 |
|---|---|
| Title | Efficacy and Safety of RTH258 Versus Aflibercept - Study 1 |
| Official title | A Two-Year, Randomized, Double-Masked, Multicenter, Three-Arm Study Comparing the Efficacy and Safety of RTH258 Versus Aflibercept in Subjects With Neovascular Age-Related Macular Degeneration |
| Acronym | HAWK |
| Lead sponsor | Alcon Research, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Neovascular Age-Related Macular Degeneration, Choroidal Neovascularization |
| Intervention type | Drug |
| Interventions | Brolucizumab ophthalmic solution, Aflibercept ophthalmic solution |
| Enrollment | 1,775 |
| Start date | Dec 8, 2014 |
| Primary completion | Apr 22, 2017 |
| Completion | Mar 28, 2018 |
| First posted | Dec 4, 2014 |
| Last update posted | Jan 16, 2025 |
| Countries | United States |
At a glance
- 1–9 Study sites
- Yes Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: