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NCT07264517 · ClinicalTrials.gov registry record · Phase 2

Evaluating the Safety, Tolerability, and Efficacy of GRF312 5% in Participants With Dry Eye Disease (DED).

A Phase 2 study of Dry Eye Disease, sponsored by Instituto Grifols, S.A..

Recruiting
Registry status
Phase 2
Development phase
100
Enrollment target
10
Study locations

NCT07264517 is a Phase 2 study of Dry Eye Disease that is actively recruiting participants, run by Instituto Grifols, S.A.. The registered enrollment target is 100 participants, below the 252-participant average among 33 other Dry Eye Disease trials with a reported enrollment target (60% lower). The trial reports 10 study locations across 7 states.

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The verdict

NCT07264517, a Phase 2 study of Dry Eye Disease, is actively recruiting participants, sponsored by Instituto Grifols, S.A..

RECRUITING
Registry status
Phase 2
Development phase
100 participants
Enrollment target
10
Study locations

Study Summary

This is a Phase 2, multi-site, double-masked, randomized, vehicle-controlled, study designed to evaluate the safety, tolerability, and efficacy in adult participants with DED.

Conditions Studied

Interventions

  • DRUG GRF312 5%
  • OTHER Placebo Comparator

Study Locations (10)

California

  • GC2302 Study Site 110 - Glendale
  • GC2302 Study Site 109 - Grove
  • GC2302 Study Site 103 - Newport Beach

North Carolina

  • GC2302 Study Site 104 - Asheville
  • GC2302 Study Site 101 - Garner

Georgia

  • GC2302 Study Site 105 - Morrow

Indiana

  • GC2302 Study Site 106 - Carmel

Pennsylvania

  • GC2302 Study Site 107 - Cranberry Township

Tennessee

  • GC2302 Study Site 102 - Memphis

Texas

  • GC2302 Study Site 111 - San Antonio

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2025-11-03
Est. Completion 2026-11-14
Phase Phase 2

Sponsor

Instituto Grifols, S.A.

10 total trials

What the Registry Record Tells You About NCT07264517

The ClinicalTrials.gov registry entry for NCT07264517 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 252-participant average among 33 other Dry Eye Disease trials with a reported enrollment target (60% lower). The listed sponsor is Instituto Grifols, S.A., which has 10 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Dry Eye Disease appearing as the primary indexed condition, and to 2 interventions - of which GRF312 5% is the first listed.

NCT07264517 reports 10 study locations spanning 7 distinct geographic areas - top geographies include California, North Carolina, Georgia.

Frequently Asked Questions

What is clinical trial NCT07264517 about?

NCT07264517 is a clinical study titled "Evaluating the Safety, Tolerability, and Efficacy of GRF312 5% in Participants With Dry Eye Disease (DED).". This is a Phase 2, multi-site, double-masked, randomized, vehicle-controlled, study designed to evaluate the safety, tolerability, and efficacy in adult participants with DED.

What is the current status of trial NCT07264517?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 100 participants. The study started on 2025-11-03. Estimated completion is 2026-11-14.

What conditions does trial NCT07264517 study?

This clinical trial studies the following conditions: Dry Eye Disease.

What interventions are being tested in trial NCT07264517?

The interventions under investigation include: GRF312 5% (DRUG), Placebo Comparator (OTHER).

Who is sponsoring clinical trial NCT07264517?

This trial is sponsored by Instituto Grifols, S.A., which has 10 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07264517 being conducted?

This trial has 10 study locations across California, Georgia, Indiana, North Carolina, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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