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Efficacy of Fusidic Acid 1% in the Treatment of Bacterial Conjunctivitis
NCT06911424 · View on ClinicalTrials.gov ↗
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 |
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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. 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 Baxis Pharmaceuticals, which has 28 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 Bacterial Conjunctivitis appearing as the primary indexed condition, and to 2 interventions — of which Placebo 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: NCT06911424 reports 20 study locations spanning 5 distinct geographic areas — top geographies include Florida, California, Arkansas. 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 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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06911424?
The interventions under investigation include: Placebo (DRUG), Fusidic Acid 1% (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06911424?
This trial is sponsored by Baxis Pharmaceuticals, which has 28 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
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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