Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02914613 · ClinicalTrials.gov registry record · Phase 1

Safety and Exploratory Efficacy Study of SF0166 for the Treatment of Diabetic Macular Edema (DME)

A Phase 1 study of Diabetic Macular Edema, sponsored by OcuTerra Therapeutics.

Completed
Registry status
Phase 1
Development phase
44
Enrollment target
6
Study locations

NCT02914613 is a Phase 1 study of Diabetic Macular Edema that has completed, run by OcuTerra Therapeutics. The registered enrollment target is 44 participants, below the 3,794-participant average among 63 other Diabetic Macular Edema trials with a reported enrollment target (99% lower). The trial reports 6 study locations across 4 states.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02914613, a Phase 1 study of Diabetic Macular Edema, has completed, sponsored by OcuTerra Therapeutics.

COMPLETED
Registry status
Phase 1
Development phase
44 participants
Enrollment target
6
Study locations

Study Summary

The primary purpose of this study was to evaluate the safety and exploratory efficacy of SF0166 Topical Ophthalmic Solution in patients with Diabetic Macular Edema (DME).

Conditions Studied

Interventions

  • DRUG SF0166 Topical Ophthalmic Solution

Study Locations (6)

California

  • Retina-Vitreous Associates Medical Group - Beverly Hills
  • United Medical Research Institute - Inglewood
  • Martel Eye Medical Group - Rancho Cordova

Florida

  • Center for Retina and Macular Disease - Winter Haven

Massachusetts

  • Ophthalmic Consultants of Boston - Boston

Texas

  • Retina Consultants of Houston - Houston

Trial Details

FieldValue
Enrollment Target 44 participants
Start Date 2016-08-24
Est. Completion 2017-05-16
Phase Phase 1

Sponsor

OcuTerra Therapeutics

3 total trials

What the Registry Record Tells You About NCT02914613

The ClinicalTrials.gov registry entry for NCT02914613 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 44 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 3,794-participant average among 63 other Diabetic Macular Edema trials with a reported enrollment target (99% lower). The listed sponsor is OcuTerra Therapeutics, which has 3 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Diabetic Macular Edema appearing as the primary indexed condition, and to 1 intervention - of which SF0166 Topical Ophthalmic Solution is the first listed.

NCT02914613 reports 6 study locations spanning 4 distinct geographic areas - top geographies include California, Florida, Massachusetts.

Frequently Asked Questions

What is clinical trial NCT02914613 about?

NCT02914613 is a clinical study titled "Safety and Exploratory Efficacy Study of SF0166 for the Treatment of Diabetic Macular Edema (DME)". The primary purpose of this study was to evaluate the safety and exploratory efficacy of SF0166 Topical Ophthalmic Solution in patients with Diabetic Macular Edema (DME).

What is the current status of trial NCT02914613?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 44 participants. The study started on 2016-08-24. Estimated completion is 2017-05-16.

What conditions does trial NCT02914613 study?

This clinical trial studies the following conditions: Diabetic Macular Edema.

What interventions are being tested in trial NCT02914613?

The interventions under investigation include: SF0166 Topical Ophthalmic Solution (DRUG).

Who is sponsoring clinical trial NCT02914613?

This trial is sponsored by OcuTerra Therapeutics, which has 3 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02914613 being conducted?

This trial has 6 study locations across California, Florida, Massachusetts, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Diabetic Macular Edema

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.