Status:

COMPLETED

Late Phase II Confirmatory Study of DE-089 Ophthalmic Solution in Patients With Dry Eye

Lead Sponsor:

Santen Pharmaceutical Co., Ltd.

Conditions:

Dry Eye

Eligibility:

All Genders

20+ years

Phase:

PHASE2

Brief Summary

Dose response related to efficacy and safety of DE-089 ophthalmic solution are examined in patients with dry eye, using a multicenter, randomized, double-blind, parallel group comparison study, and th...

Eligibility Criteria

Inclusion

  • Those who show:
  • Keratoconjunctival disorder confirmed with vital dye staining
  • Abnormal Schirmer score results

Exclusion

  • Eye disease that needs therapy other than that for dry eye
  • Those who need to wear contact lenses during the clinical study

Key Trial Info

Start Date :

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

Estimated Enrollment :

320 Patients enrolled

Trial Details

Trial ID

NCT01189032

Last Update

August 13 2014

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Santen study sites

Osaka, Osaka, Japan