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A Clinical Trial to study the effects of NVC-422 Ophthalmic Solution for the Treatment of Adenoviral Conjunctivitis

Phase 2
Conditions
Health Condition 1: null- Adenoviral Conjunctivitis
Registration Number
CTRI/2012/11/003145
Lead Sponsor
ovaBay Pharmaceutical Inc
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
440
Inclusion Criteria

1. Subjects must be >= 18 years of age and <= 65 years of age

2. At least 1 eye (and in that same eye) must have onset and development of ocular symptoms and/or signs of conjunctivitis <= 3 days prior to enrollment (Day 1)

3. Females who are not pregnant and are not lactating.

4. Other inclusion criteria per protocol.

Exclusion Criteria

1.Presence of subepithelial infiltrates (SEIs) at the Day 1 visit in either eye.

2.Suspected bacterial, fungal, herpes, Chlamydia or Acanthamoeba co-infection, based on clinical observation.

3.Subjects with ocular condition(s) that may interfere with the conduct of the study as outlined in the protocol.

4.Other exclusion criteria per protocol.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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