Xalacom
DrugXalacom 1 drop into the affected eye daily
NCT Number: NCT00801437
This study is designed to evaluate the safety and tolerability of Xalacom in patients with primary glaucoma
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Notify Me18 year–99 year
All sexes
Observational
Pfizer Investigational Site, Banovce N. Bebravou, Slovakia
according to physicians decision, patients who met inclusion and exclusion criteria and sign the ICD
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Xalacom 1 drop into the affected eye daily
Time frame: 12 months
Time frame: 12 months
Time frame: 12 months
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
Industry
Non Interventional Study in Slovak Patients With Primary Open Angle Glaucoma and/or Ocular Hypertension Treated With Xalacom® After Failure of Previous Antiglaucoma Therapy Due to Ineffectivity or Intolerance.
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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