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Clinical Trials/CTRI/2012/11/003145
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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
ovaBay Pharmaceutical Inc

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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