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Clinical Trial Summary

Santen will evaluate the intraocular pressure (IOP) lowering effect and efficacy of DE-117 ophthalmic solution 0.002% in latanoprost low/non-responder subjects diagnosed with POAG or OHT


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03697811
Study type Interventional
Source Santen Inc.
Contact
Status Completed
Phase Phase 3
Start date September 27, 2018
Completion date January 13, 2022

See also
  Status Clinical Trial Phase
Completed NCT03858894 - Study Assessing the Safety and Efficacy of DE-117 Ophthalmic Solution Once Daily and Twice Daily in Subjects With Primary Open-Angle Glaucoma SPECTRUM 6 Phase 2