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

This study has been completed.

Sponsored by: Sirion Therapeutics, Inc.
Information provided by: Sirion Therapeutics, Inc.
ClinicalTrials.gov Identifier: NCT00549289
  Purpose

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.


Condition Intervention Phase
Dry Eye Syndromes
Drug: cyclosporine A
Phase III

ChemIDplus related topics:   Cyclosporine    Cyclosporin   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Open Label, Single Group Assignment
  Eligibility
Ages Eligible for Study:   2 Years and older
Genders Eligible for Study:   Both

Criteria

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
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00549289

Locations
United States, Georgia
Clayton Eye Center    
      Morrow, Georgia, United States, 30260

Sponsors and Collaborators
Sirion Therapeutics, Inc.

Investigators
Study Chair:     Roger Vogel     Sirion Therapeutics    
  More Information


Study ID Numbers:   ST-603-006
First Received:   October 24, 2007
Last Updated:   October 24, 2007
ClinicalTrials.gov Identifier:   NCT00549289
Health Authority:   United States: Food and Drug Administration

Study placed in the following topic categories:
Cyclosporine
Clotrimazole
Miconazole
Eye Diseases
Tioconazole
Lacrimal Apparatus Diseases
Dry Eye Syndromes
Cyclosporins

Additional relevant MeSH terms:
Anti-Infective Agents
Disease
Molecular Mechanisms of Pharmacological Action
Immunologic Factors
Physiological Effects of Drugs
Enzyme Inhibitors
Immunosuppressive Agents
Pharmacologic Actions
Pathologic Processes
Syndrome
Antifungal Agents
Therapeutic Uses
Antirheumatic Agents
Dermatologic Agents

ClinicalTrials.gov processed this record on October 17, 2008




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