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Long-Term Non-Interventional Latanoprost Study

Type: Observational

Status of the trial: Completed

Orphan Drug Recognition: No


  • Opening Date: 2010-12-23
  • Closing Date: 2017-10-12


Inclusion: Diagnosis of pediatric glaucoma or elevated intraocular pressure, continuously treated with latanoprost for at least 1 month within the year prior to the baseline examination

Exclusion: Pregnant or nursing females at baseline, a history of allergy or hypersensitivity to any of the ingredients contained in latanoprost

More information

Children: Yes

Adults: No

Funder Type: industry

HCP: Other investigators

Within ERN-EYE members

Principal investigators

Other investigators


  • Neuro-Ophthalmology Rare Diseases (WG2)

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This ERN is supported by: