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Phase 4 study comparing IOP lowering in OAG or OH in Caucasian or Japanese subjects C-02-32



Phase 4 study comparing IOP lowering in OAG or OH in Caucasian or Japanese subjects C-02-32

For Condition: Open-Angle Glaucoma,Ocular Hypertension
Status: Recruiting
Sponsor(s): Alcon Research ,
Synopsis: The purpose of this study is to evaluate safety and efficacy of two different IOP lowering medications after six weeks of treatment in Caucasian and Japanese subjects.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Safety/Efficacy Study
Minimum Age/Maximum Age: 18 Years/
Genders: Both
Protocol Entry Criteria: Adults of Caucasian and Japanese Ethnicity
Total Enrollment: 

Location and Contact Information:


Additional Information:
Study ID Numbers:
  C-02-32;  C-02-32
Study Start Date: 
Record last reviewed: November 2002
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00047606

Other Open-Angle Glaucoma Studies:
1. Phase II safety and efficacy study to evaluate a glaucoma therapy in open-angle glaucoma or ocular hypertension patients

2. Phase IV study of TRAVATAN 0.004% in subjects with iris pigmentation changes

3. Phase 3 study to evaluate IOP lowering therapy in open angle glaucoma and ocular hypertension C-01-70

4. Phase 3 study to evaluate IOP lowering therapy in open angle glaucoma and ocular hypertension C-01-69

5. A Phase III Study of Brimonidine Tartrate Ophthalmic Solution, 0.15% in Patients with Open-Angle Glaucoma or Ocular Hypertension

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Phase 4 study comparing IOP lowering in OAG or OH in Caucasian or Japanese subjects C-02-32

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