A Study to Determine the Safety and Tolerability of Escalating Doses of INS365 Ophthalmic Solution

NCT00680108 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 62

Last updated 2015-08-27

No results posted yet for this study

Summary

The purpose of this study is to evaluate the safety and tolerability of INS365 Ophthalmic Solution when applied topically as eyedrops in patients with mild to moderate dry eye disease.

Conditions

Interventions

DRUG

diquafosol tetrasodium (INS365) ophthalmic solution

Sponsors & Collaborators

Principal Investigators

  • Clinical Director · Merck Sharp & Dohme LLC

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Sex
Healthy Volunteers
No

Timeline & Regulatory

Start
1999-09-30
Primary Completion
2000-05-31
Completion
2000-05-31

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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 NCT00680108 on ClinicalTrials.gov