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Clinical Trial

Safety and Efficacy Study of RTP-008 (an Absorbable Tacrolimus Lacrimal Canalicular Plug) for Dry Eye

NCT: NCT07806240 · COMPLETED

NCT IDNCT07806240
StatusCOMPLETED
Start Date2025-04-08
Completion2026-02-28
SponsorZhejiang Raytone Bioscience Co.,Ltd (INDUSTRY)
First posted
Last updated

Brief Summary

RTP-008, an absorbable tacrolimus lacrimal canalicular plug, targets two key pathophysiological mechanisms of dry eye: tear retention and local anti-inflammation. This clinical trial aims to evaluate the safety and efficacy of RTP-008 in adults with moderate to severe dry eye. The main questions it aims to answer are: * Is RTP-008 safe for the eyes? * How well does the plug work to improve dry eye? * Which size provides a better fit for the human lacrimal canaliculus after swelling? Participants will be divided into three groups: * Two groups will receive RTP-008 inserted into their lacrimal canaliculus (in two slightly different sizes). * One comparison group will receive an already approved dissolvable plug. All participants will use a standard lubricating eye drop four times a day in both eyes. All participants will attend follow-up visits for 24 weeks so doctors can check their eye health and any side effects.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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