Efficacy and Safety Assessment of T4032 (Unpreserved Bimatoprost 0.01%) Versus Lumigan® 0.01% in Ocular Hypertensive or Glaucomatous Patients

In by Hannah Schaffner

Efficacy and Safety Assessment of T4032 (Unpreserved Bimatoprost 0.01%) Versus Lumigan® 0.01% in Ocular Hypertensive or Glaucomatous Patients

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Efficacy and Safety Assessment of T4032 (Unpreserved Bimatoprost 0.01%) Versus Lumigan® 0.01% in Ocular Hypertensive or Glaucomatous Patients

clinicaltrials.gov

Eligibility

Inclusion Criteria
  1. Informed consent dated and signed.
  2. Both eyes diagnosed open-angle glaucoma or ocular hypertension
Exclusion Criteria
  1. History of trauma, infection, clinically significant inflammation within the previous 3 months
  2. Known or suspected hypersensitivity to one of the components of the Investigational Medicinal Product(s)
  3. Pregnancy or breast-feeding
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