# A Phase 3 Safety and Efficacy Study of Fovista® (E10030) Intravitreous Administration in Combination With Lucentis® Compared to Lucentis® Monotherapy

> **NCT01940900** · PHASE3 · TERMINATED · sponsor: **Ophthotech Corporation** · enrollment: 627 (actual)

## Conditions studied

- Age-Related Macular Degeneration

## Interventions

- **DRUG:** E10030
- **DRUG:** ranibizumab
- **DRUG:** E10030 sham intravitreal injection

## Key facts

- **NCT ID:** NCT01940900
- **Lead sponsor:** Ophthotech Corporation
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE3
- **Study type:** INTERVENTIONAL
- **Status:** TERMINATED
- **Start date:** 2013-08
- **Primary completion:** 2016-12
- **Final completion:** 2016-12
- **Target enrollment:** 627 (ACTUAL)
- **Last updated:** 2024-10-30


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01940900

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01940900, "A Phase 3 Safety and Efficacy Study of Fovista® (E10030) Intravitreous Administration in Combination With Lucentis® Compared to Lucentis® Monotherapy". Retrieved via AI Analytics 2026-06-01 from https://api.ai-analytics.org/clinical/NCT01940900. Licensed CC0.

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