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ACTIVE NOT RECRUITING Phase 3

Epithelium-On Corneal Cross-linking in Subjects 8 to 45 Years of Age With Keratoconus

NCT06100939 · View on ClinicalTrials.gov ↗

Study Summary

A Multicenter, Randomized, Double-Masked, Sham-Controlled, Parallel-Group Phase 3 Study to Evaluate the Efficacy and Safety of Epithelium-On Corneal Cross-linking in Subjects 8 to 45 Years of Age With Keratoconus

Conditions Studied

Interventions

  • COMBINATION_PRODUCT Riboflavin and Sodium Iodide solution and Ultraviolet-A treatment
  • COMBINATION_PRODUCT Placebo and sham treatment

Study Locations (13)

California

  • Nvision Eye Centers Rowland Heights — Rowland Heights
  • Goodman Eye Center — San Francisco

Pennsylvania

  • Wills Eye Hospital — Philadelphia
  • UPMC Vision Institute — Pittsburgh

Florida

  • Center for Excellence in Eye Care — Miami

Illinois

  • Chicago Cornea Consultants — Hoffman Estates

Massachusetts

  • Boston Vision — Brookline

Missouri

  • Ophthalmology Associates — St Louis

New York

  • The Eye Doctors at CNY Eye Care — East Syracuse

Ohio

  • Cincinnati Eye Institute — Cincinnati

Trial Details

FieldValue
Enrollment Target 400 participants
Start Date 2023-10-30
Est. Completion 2025-10
Phase Phase 3

Sponsor

Epion Therapeutics

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06100939

The ClinicalTrials.gov registry entry for NCT06100939 describes a study currently listed as active not recruiting. It is categorized as Phase 3, 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 400 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Epion 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 Keratoconus appearing as the primary indexed condition, and to 2 interventions — of which Riboflavin and Sodium Iodide solution and Ultraviolet-A treatment 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: NCT06100939 reports 13 study locations spanning 11 distinct geographic areas — top geographies include California, Pennsylvania, 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 NCT06100939 about?

NCT06100939 is a clinical study titled "Epithelium-On Corneal Cross-linking in Subjects 8 to 45 Years of Age With Keratoconus". A Multicenter, Randomized, Double-Masked, Sham-Controlled, Parallel-Group Phase 3 Study to Evaluate the Efficacy and Safety of Epithelium-On Corneal Cross-linking in Subjects 8 to 45 Years of Age With Keratoconus

What is the current status of trial NCT06100939?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 400 participants. The study started on 2023-10-30. Estimated completion is 2025-10.

What conditions does trial NCT06100939 study?

This clinical trial studies the following conditions: Keratoconus. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06100939?

The interventions under investigation include: Riboflavin and Sodium Iodide solution and Ultraviolet-A treatment (COMBINATION_PRODUCT), Placebo and sham treatment (COMBINATION_PRODUCT). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06100939?

This trial is sponsored by Epion 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 NCT06100939 being conducted?

This trial has 13 study locations across California, Florida, Illinois, Massachusetts, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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