Efficacy and Tolerability of Xalatan in Patients

Overview

Efficacy data was not collected or analyzed. This study did assess safety and tolerability of Xalatan.

Full Title of Study: “Observational Study Assessing The Efficacy And Tolerability Of Xalatan™ In Patients With Open Angle Glaucoma And /Or Ocular Hypertension.”

Study Type

  • Study Type: Observational
  • Study Design
    • Time Perspective: Prospective
  • Study Primary Completion Date: December 2007

Detailed Description

– Efficacy data not collected or analyzed – Safety and tolerability of Xalatan assessed NA

Interventions

  • Drug: Xalatan 0.005% eye drops
    • ophthalmic solution dosed once daily for 3 months

Arms, Groups and Cohorts

  • Study Drug – Xalatan 0.005% eye drops

Clinical Trial Outcome Measures

Primary Measures

  • Intraocular Pressure
    • Time Frame: Screening, 10 days, 4 weeks and 12 weeks after beginning treatment
    • Intraocular pressure was measured at each visit
  • Humphrey Perimetry Visual Field
    • Time Frame: Visits 1 and 4
    • Analysis of visual field deficits for abnormalities.

Participating in This Clinical Trial

Inclusion Criteria

  • Patient with ocular hypertension at least 22mg Hg – Patient must be over 18 years old Exclusion Criteria:

  • None listed in the protocol

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: 65 Years

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Pfizer’s Upjohn has merged with Mylan to form Viatris Inc.
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Official(s)
    • Pfizer CT.gov Call Center, Study Director, Pfizer

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