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

  • End date
    Aug 31, 2023
  • participants needed
  • sponsor
    Laboratoires Thea
Updated on 4 October 2022


The main study purpose is to demonstrate the non-inferiority of T4032 compared to Lumigan® 0.01% in terms of efficacy.

Condition Glaucoma, Ocular Hypertension
Treatment Bimatoprost Ophthalmic
Clinical Study IdentifierNCT05397600
SponsorLaboratoires Thea
Last Modified on4 October 2022


Yes No Not Sure

Inclusion Criteria

Informed consent dated and signed
Both eyes diagnosed open-angle glaucoma or ocular hypertension

Exclusion Criteria

History of trauma, infection, clinically significant inflammation within the previous 3 months
Known or suspected hypersensitivity to one of the components of the Investigational Medicinal Product(s)
Pregnancy or breast-feeding
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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