Clinical and Microbial Efficacy of ISV403 in Bacterial Conjunctivitis

Bacterial Conjunctivitis Clinical Trial

Official title:

A Study to Evaluate the Clinical and Microbial Efficacy of 0.6% ISV-403 Compared to Vehicle in the Treatment of Bacterial Conjunctivitis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00622908
• Other study ID #: 373
• Status: Completed
• Phase: Phase 2
• First received: February 14, 2008
• Last updated: March 4, 2015
• Start date: December 2004
• Est. completion date: June 2005

Study information

• Verified date: March 2015
• Source: Bausch & Lomb Incorporated
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

To evaluate the clinical and microbial efficacy of ISV-403 administered three times a day (TID) for 5 days compared to vehicle three times a day for 5 days in the treatment of bacterial conjunctivitis

Recruitment information / eligibility

• Status: Completed
• Enrollment: 270
• Est. completion date: June 2005
• Est. primary completion date: June 2005
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 1 Year and older

Eligibility

Inclusion Criteria:

• Must be at least one year of age.

• Must have signature of subject or legally authorized representative (if subject is under 18 years of age) on the informed Consent Form.

• Must have signature of subject on the Assent Form if subject is 6 to 17 years of age.

• Must have a clinical diagnosis of acute bacterial conjunctivitis and exhibit purulent conjunctival discharge (crusty or sticky eyelids) and redness in at least one eye. A minimum score of 1 should be present for discharge and a minimum score of 1 for either bulbar or palpebral conjunctival injection.

• Must have pinholed visual acuity equal to or better than 20/200 in both eyes. Age appropriate visual acuity testing was to be performed. Every effort was made to obtain a visual acuity measurement in children. If visual acuity was unobtainable in children, it was at the investigator's discretion to meet inclusion criteria.

• Must be willing to discontinue contact lens wear for the duration of the study.

• Must be willing to avoid disallowed medications during the study period.

• Must understand the scope of the study including completion of diary, be willing to follow instructions, and be able to make all required study visits.

• If a subject was a female of childbearing potential, she must utilize reliable contraceptive methods and have a negative pregnancy test.

Exclusion Criteria:

• Any uncontrolled systemic disease or debilitating disease.

• Use of topical ophthalmic solutions including tear substitutes within two hours before and during the study.

• Use of any ophthalmic topical anti-inflammatory agents within 48 hours before and during the study.

• Subjects likely to require antimicrobial therapy with any active respiratory tract infection, urinary tract infection, skin/soft tissue infection, or otitis media.

• Pregnant or nursing females.

• Known hypersensitivity to SS734 or to any of the ingredients in the study medications.

• Known hypersensitivity to fluoroquinolones or to any of the ingredients in the study medications.

• Ocular surgery (including laser surgery) in either eye within the past six weeks.

• Subjects with suspected viral or allergic conjunctivitis (i.e., severe itching or acute follicular conjunctivitis), or any other disease conditions that could interfere with the efficacy and safety evaluations of the study medication.

• Subjects with suspected iritis (i.e., smaller pupil, pain, and photophobia in infected eye).

• History of recurrent corneal erosion syndrome, either idiopathic or secondary to previous corneal trauma or dry eye syndrome.

• Use of any antibiotic within 72 hours of enrollment.

• Any active ulcerative keratitis, specifically any epithelial loss greater than punctate keratitis

• Participation in an ophthalmic drug or device research study within the 30 days prior to entry in this study.

• Subjects who were immune compromised.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Bacterial Conjunctivitis
• Conjunctivitis
• Conjunctivitis, Bacterial

Intervention

Drug:
• ISV-403
0.6% TID, 5 days
• Vehicle
Vehicle of ISV-403 TID, 5 days

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Bausch & Lomb Incorporated

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Clinical Resolution of Baseline Bacterial Conjunctivitis (Day 8 or 9)	Resolution of conjunctival discharge, bulbar conjunctival injection and palpebral conjunctival injection.	Visit 3 - day 8 or 9	No
Primary	Eradication of Baseline Pathogens (Day 8 or 9)	Bacterial species eradication of baseline bacterial infection	Visit 3 - Day 8 or day 9	No
Secondary	Clinical Resolution of Baseline Bacterial Conjunctivitis Day 4 (+/- 1 Day)	The absence of conjunctival discharge, bulbar conjunctival injection and palpebral conjunctival injection.	Visit 2 - Day 4 (+/- 1 day)	No
Secondary	Eradication of Baseline Pathogens Day 4 (+/- 1 Day)	Bacterial species eradication of baseline bacterial infection	Visit 2 - Day 4 (+/- 1 day)	No