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Clinical Trial Summary

This is a multi-center, open-label, single dose/multiple dose, pharmacokinetic study in participants with bacterial conjunctivitis. The purpose of this study is to determine the extent of systemic exposure to BOL-303224-A following single and multiple topical administration of BOL-303224-A in participants with suspected bacterial conjunctivitis.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Pharmacokinetics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00407589
Study type Interventional
Source Bausch & Lomb Incorporated
Contact
Status Completed
Phase Phase 1
Start date October 2006
Completion date October 2007

See also
  Status Clinical Trial Phase
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Completed NCT03987178 - Microbiologic Alterations of the Conjunctiva of Hot Tub-soaking Ophthalmologists N/A
Completed NCT00357773 - Efficacy and Safety of T1225 1.5% Versus Tobramycin 0.3 % in the Treatment of Purulent Bacterial Conjunctivitis Phase 3
Completed NCT03519516 - Safety and Tolerability of the PRO-174 Versus Sophixín Ofteno®, on the Ocular Surface of Healthy Subjects Phase 1
Withdrawn NCT01721694 - Antibiotic Steroid Combination Compared With Individual Administration in the in the Treatment of Ocular Inflammation and Infection Phase 3