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Clinical Trial Summary

This study is conducted to evaluate the safety of THR-317 when administered intravitreally and to assess the compound's efficacy in improving best-corrected visual acuity (BCVA) and reducing central subfield thickness (CST) in subjects with centre-involved diabetic macular oedema (DME).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03071068
Study type Interventional
Source ThromboGenics
Contact
Status Completed
Phase Phase 2
Start date December 22, 2016
Completion date April 2018

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