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Study of Cyclosporine in the Treatment of Dry Eye Syndrome (ST-603-006)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00549289
First Posted: October 25, 2007
Last Update Posted: October 25, 2007
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Sirion Therapeutics, Inc.
October 24, 2007
October 25, 2007
October 25, 2007
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No Changes Posted
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Study of Cyclosporine in the Treatment of Dry Eye Syndrome (ST-603-006)
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The purpose of this phase III, open-label study is to determine the safety and tolerability of cyclosporine in the treatment of dry eye syndrome.
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Interventional
Phase 3
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Dry Eye Syndromes
Drug: cyclosporine A
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
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Inclusion Criteria:

  • Diagnosis of dry eye syndrome

Exclusion Criteria:

  • Intraocular or refractive surgery in the study eye within 3 months prior to study start
  • Unwilling to discontinue use of contact lenses during the study
  • Pregnancy or lactation
Sexes Eligible for Study: All
2 Years and older   (Child, Adult, Senior)
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Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00549289
ST-603-006
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Sirion Therapeutics, Inc.
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Study Chair: Roger Vogel Sirion Therapeutics
Sirion Therapeutics, Inc.
October 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP