Post-approval study to assess Lamelleye vs comparator for the treatment of dry eye disease in adults

Project Details

Description

The purpose of the study is to investigate the safety and tolerability of repeat ocular dosing of the investigational product LMS-611.
StatusFinished
Effective start/end date25/11/16 → 31/07/18

Funding

  • Lamellar Biomedical Ltd: £39,925.00
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