A Clinical Trial to study the effects of NVC-422 Ophthalmic Solution for the Treatment of Adenoviral Conjunctivitis
- 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
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.
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
Name Time Method
- Secondary Outcome Measures
Name Time Method