CTRI/2012/11/003145
Recruiting
Phase 2
A Multicenter, Randomized Study of the Efficacy and Safety of NVC-422 Ophthalmic Solution for the Treatment of Adenoviral Conjunctivitis
ovaBay Pharmaceutical Inc0 sites440 target enrollmentTBD
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- ovaBay Pharmaceutical Inc
- Enrollment
- 440
- Status
- Recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
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.
Outcomes
Primary Outcomes
Not specified
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