TerminatedPhase 3NCT01740388
Clinical and Microbial Efficacy of Besifloxacin Ophthalmic Suspension, 0.6% in the Treatment of Bacterial Conjunctivitis
Studying Body integrity dysphoria
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Bausch & Lomb Incorporated
- Principal Investigator
- Johnson VarugheseValeant Pharmaceuticals/Bausch & Lomb Incorporated
- Intervention
- Besifloxacin(drug)
- Enrollment
- 136 target
- Eligibility
- 1 years · All sexes
- Timeline
- 2013 – 2013
Study locations (1)
- Bausch & Lomb Incorporated, Rochester, New York, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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