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Clinical Trial Summary

The purpose of this study is to evaluate the safety and efficacy of two different concentrations of the new formulation of rhNGF ophthalmic solution versus vehicle, in order to demonstrate superiority of at least one of the two concentrations over vehicle in the improvement of ocular symptoms of dry eye in participants with dry eye disease (DED). The rhNGF ophthalmic solution, or vehicle, will be administered as one drop in each eye, three times a day, for 4 weeks. Participants will attend a total of 5 study visits from screening through end of the study (Week 8), which will include eye exams and questionnaires.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06244316
Study type Interventional
Source Dompé Farmaceutici S.p.A
Contact Marta Sacchetti, MD
Phone +39 34 76757333
Email marta.sacchetti@dompe.com
Status Recruiting
Phase Phase 2
Start date January 22, 2024
Completion date September 2024

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