CompletedPhase 1NCT01658839

Pharmacokinetic and Safety Study of Travoprost 0.004% in Pediatric Glaucoma Patients

Studying Congenital glaucoma

Last synced from ClinicalTrials.gov

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Key facts

Sponsor
Alcon Research
Principal Investigator
Subha Venkataraman
Alcon Research
Intervention
Travoprost ophthalmic solution, 0.004% (new formulation)(drug)
Enrollment
25 enrolled
Eligibility
17 years · All sexes
Timeline
20132013

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT01658839 on ClinicalTrials.gov

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