Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
Safety and Exploratory Efficacy Study of SF0166 in the Treatment of Neovascular Age-Related Macular Degeneration (AMD)
NCT02914639 · View on ClinicalTrials.gov ↗
Study Summary
The primary purpose of this study was to evaluate the safety and exploratory efficacy of SF0166 Topical Ophthalmic Solution in patients with Neovascular (wet) Age-related Macular Degeneration (AMD).
Conditions Studied
Interventions
- DRUG SF0166 Topical Ophthalmic Solution
Study Locations (12)
Texas
- West Texas Retina Consultants — Abilene
- Retina Research Center, PLLC — Austin
- Texas Retina Associates — Fort Worth
California
- Retina Consultants of Orange County — Fullerton
- Northern California Retina Vitreous Associates Medical Group, Inc — Mountain View
Florida
- Retina Macula Specialists of Miami, LLC — Miami
- Center for Retina and Macular Disease — Winter Haven
Arizona
- Retinal Research Institute LLC — Phoenix
Indiana
- John Kenyon Eye Institute — New Albany
Massachusetts
- Ophthalmic Consultants of Boston — Boston
South Dakota
- Black Hills Regional Eye Institute — Rapid City
Washington
- Spokane Eye Clinical Research — Spokane
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 44 participants |
| Start Date | 2016-10-05 |
| Est. Completion | 2017-06-26 |
| Phase | Phase 1 |
Interested in This Trial?
Always speak with your doctor before enrolling in a clinical trial.
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02914639
The ClinicalTrials.gov registry entry for NCT02914639 describes a study currently listed as completed. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 44 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is OcuTerra Therapeutics, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Age-Related Macular Degeneration appearing as the primary indexed condition, and to 1 intervention — of which SF0166 Topical Ophthalmic Solution is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT02914639 reports 12 study locations spanning 8 distinct geographic areas — top geographies include Texas, California, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT02914639 about?
NCT02914639 is a clinical study titled "Safety and Exploratory Efficacy Study of SF0166 in the Treatment of Neovascular Age-Related Macular Degeneration (AMD)". The primary purpose of this study was to evaluate the safety and exploratory efficacy of SF0166 Topical Ophthalmic Solution in patients with Neovascular (wet) Age-related Macular Degeneration (AMD).
What is the current status of trial NCT02914639?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 44 participants. The study started on 2016-10-05. Estimated completion is 2017-06-26.
What conditions does trial NCT02914639 study?
This clinical trial studies the following conditions: Age-Related Macular Degeneration. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT02914639?
The interventions under investigation include: SF0166 Topical Ophthalmic Solution (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT02914639?
This trial is sponsored by OcuTerra Therapeutics, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT02914639 being conducted?
This trial has 12 study locations across Arizona, California, Florida, Indiana, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
How Clinical Trials Work
Understand phases 1-4, trial design, randomization, and the informed consent process.
Patient Rights in Clinical Trials
Your rights as a participant: consent, withdrawal, privacy, and who to contact.
Finding the Right Clinical Trial
A practical guide to searching trials, understanding eligibility, and evaluating options.
All Guides
Browse our complete library of clinical trial educational resources.
Read our methodology — how this data is sourced, computed, and verified.