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Clinical Trial Summary

- To assess the efficacy of R348 Ophthalmic Solutions administered for 12 weeks to subjects evaluated by objective and subjective measures.

- To investigate the safety and tolerability of R348 Ophthalmic Solutions administered for 12 weeks to subjects.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT02040623
Study type Interventional
Source Rigel Pharmaceuticals
Contact
Status Completed
Phase Phase 2
Start date March 2014
Completion date July 2016

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