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NCT06911424 · ClinicalTrials.gov registry record · Phase 3
Efficacy of Fusidic Acid 1% in the Treatment of Bacterial Conjunctivitis
A Phase 3 study of Bacterial Conjunctivitis, sponsored by Baxis Pharmaceuticals.
- Recruiting
- Registry status
- Phase 3
- Development phase
- 400
- Enrollment target
- 20
- Study locations
NCT06911424 is a Phase 3 study of Bacterial Conjunctivitis that is actively recruiting participants, run by Baxis Pharmaceuticals. The registered enrollment target is 400 participants, below the 568-participant average among 7 other Bacterial Conjunctivitis trials with a reported enrollment target (30% lower). The trial reports 20 study locations across 5 states.
The verdict
NCT06911424, a Phase 3 study of Bacterial Conjunctivitis, is actively recruiting participants, sponsored by Baxis Pharmaceuticals.
- RECRUITING
- Registry status
- Phase 3
- Development phase
- 400 participants
- Enrollment target
- 20
- Study locations
Study Summary
The purpose of this clinical trial is to demonstrate the superiority of fusidic acid 1% over placebo in adults and children with confirmed bacterial conjunctivitis and to further establish the safety profile of fusidic acid 1% for topical ocular administration.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG Fusidic Acid 1%
Study Locations (20)
Florida
- Baxis Site 34 - Delray Beach
- Baxis Site 22 - Doral
- Baxis Site 11 - Lake Worth
- Baxis Site 37 - Largo
- Baxis Site 27 - Lutz
- Baxis Site 01 - Miami
- Baxis Site 03 - Miami
- Baxis Site 13 - Miami Beach
- Baxis Site 28 - Miami Lakes
- Baxis Site 29 - Palm Springs
- Baxis Site 10 - Tampa
California
- Baxis Site 24 - Huntington Beach
- Baxis Site 19 - La Jolla
- Baxis Site 39 - Long Beach
- Baxis Site 31 - Los Angeles
- Baxis Site 38 - Los Angeles
- Baxis Site 20 - Sherman Oaks
Arkansas
- Baxis Site 04 - Little Rock
Georgia
- Baxis Site 35 - Union City
Idaho
- Baxis Site 15 - Idaho Falls
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 400 participants |
| Start Date | 2025-03-21 |
| Est. Completion | 2026-03-23 |
| Phase | Phase 3 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06911424
The ClinicalTrials.gov registry entry for NCT06911424 describes a study currently listed as recruiting, categorized as Phase 3. The registered enrollment target is 400 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 568-participant average among 7 other Bacterial Conjunctivitis trials with a reported enrollment target (30% lower). The listed sponsor is Baxis Pharmaceuticals, which has 1 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Bacterial Conjunctivitis appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.
NCT06911424 reports 20 study locations spanning 5 distinct geographic areas - top geographies include Florida, California, Arkansas.
Frequently Asked Questions
What is clinical trial NCT06911424 about?
NCT06911424 is a clinical study titled "Efficacy of Fusidic Acid 1% in the Treatment of Bacterial Conjunctivitis". The purpose of this clinical trial is to demonstrate the superiority of fusidic acid 1% over placebo in adults and children with confirmed bacterial conjunctivitis and to further establish the safety profile of fusidic acid 1% for topical ocular administration.
What is the current status of trial NCT06911424?
This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 400 participants. The study started on 2025-03-21. Estimated completion is 2026-03-23.
What conditions does trial NCT06911424 study?
This clinical trial studies the following conditions: Bacterial Conjunctivitis.
What interventions are being tested in trial NCT06911424?
The interventions under investigation include: Placebo (DRUG), Fusidic Acid 1% (DRUG).
Who is sponsoring clinical trial NCT06911424?
This trial is sponsored by Baxis Pharmaceuticals, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06911424 being conducted?
This trial has 20 study locations across Arkansas, California, Florida, Georgia, Idaho. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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.