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A Phase 1/2 Crossover Study to Assess EXP039 for Myopia or Hyperopia

Myopia Clinical Trial

Official title:
A Phase 1/2, Randomized, Placebo Controlled Crossover Study to Assess the Safety, Pharmacodynamics, and Efficacy of EXP039 Ophthalmic Solution in Participants With Myopia or Hyperopia

Clinical Trial Summary

Assess the Safety, Pharmacodynamics, and Efficacy of EXP039 Ophthalmic Solution in Participants with Myopia or Hyperopia

Clinical Trial Description

To characterize the effect of pupillary miosis as achieved with EXP039 1% ophthalmic solution in terms of mean number of lines (Early Treatment Diabetic Retinopathy Study [ETDRS]) of improvement from baseline in binocular (both eyes open) mesopic high-contrast uncorrected distance visual acuity (UDVA) at 1-hour post treatment. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04883996
Study type Interventional
Source Canyon City Eyecare
Contact
Status Enrolling by invitation
Phase Phase 1/Phase 2
Start date December 1, 2020
Completion date August 30, 2021
View Details
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