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NCT01940887 · ClinicalTrials.gov registry record · Phase 3
A Phase 3 Safety and Efficacy Study of Fovista® (E10030) Intravitreous Administration in Combination With Either Avastin® or Eylea® Compared to Avastin® or Eylea® Monotherapy
A Phase 3 study, sponsored by Ophthotech Corporation.
- Terminated
- Registry status
- Phase 3
- Development phase
- 645
- Enrollment target
NCT01940887: Clinical Trial Phase 3 study, sponsored by Ophthotech Corporation.
NCT01940887 is a Phase 3 study that was terminated before completion, run by Ophthotech Corporation. The registered enrollment target is 645 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01940887, a Phase 3 study, was terminated before completion, sponsored by Ophthotech Corporation.
- TERMINATED
- Registry status
- Phase 3
- Development phase
- 645 participants
- Enrollment target
Study Summary
The objectives of this study are to evaluate the safety and efficacy of intravitreal administration of Fovista® administered in combination with either Avastin® or Eylea® compared to Avastin® or Eylea® monotherapy in subjects with subfoveal choroidal neovascularization secondary to age-related macular degeneration (AMD).
Interventions
- DRUG E10030
- DRUG bevacizumab or aflibercept
- DRUG E10030 sham injection
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 645 participants |
| Start Date | 2014-05 |
| Est. Completion | 2017-09 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01940887
The ClinicalTrials.gov registry entry for NCT01940887 describes a study currently listed as terminated, categorized as Phase 3. The registered enrollment target is 645 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ophthotech Corporation, which has 11 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which E10030 is the first listed.
NCT01940887 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01940887 about?
NCT01940887 is a clinical study titled "A Phase 3 Safety and Efficacy Study of Fovista® (E10030) Intravitreous Administration in Combination With Either Avastin® or Eylea® Compared to Avastin® or Eylea® Monotherapy". The objectives of this study are to evaluate the safety and efficacy of intravitreal administration of Fovista® administered in combination with either Avastin® or Eylea® compared to Avastin® or Eylea® monotherapy in subjects with subfoveal choroidal neovascularization secondary to age-related macul...
What is the current status of trial NCT01940887?
This trial is currently terminated. It is a Phase 3 study. The enrollment target is 645 participants. The study started on 2014-05. Estimated completion is 2017-09.
What interventions are being tested in trial NCT01940887?
The interventions under investigation include: E10030 (DRUG), bevacizumab or aflibercept (DRUG), E10030 sham injection (DRUG).
Who is sponsoring clinical trial NCT01940887?
This trial is sponsored by Ophthotech Corporation, which has 11 total clinical trials registered on ClinicalTrials.gov.
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