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Clinical Trial Summary

This is a proof of mechanism trial to explore the effect of BI 1026706 on the central retinal thickness and to evaluate safety and tolerability of BI 1026706 administered orally for 12 weeks in patients with mild vision impairment due to center-involved DME


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02732951
Study type Interventional
Source Boehringer Ingelheim
Contact
Status Completed
Phase Phase 2
Start date April 14, 2016
Completion date October 24, 2017

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