Study of INS365 Ophthalmic Solution in a Controlled Adverse Environment in Patients With Dry Eye

NCT00037661 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 222

Last updated 2015-10-02

No results posted yet for this study

Summary

Comparative efficacy trial of INS365 Ophthalmic Solution and placebo in patients with dry eye.

Conditions

  • Keratoconjunctivitis Sicca

Interventions

DRUG

INS365 Ophthalmic Solution

Sponsors & Collaborators

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2002-04-30
Primary Completion
2003-03-31
Completion
2003-03-31

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00037661 on ClinicalTrials.gov