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About
In this prospective, Phase 2, randomized, double-masked, vehicle controlled study, approximately 66 eligible subjects will be randomized 1:1 to receive either TL-925 or placebo as topical ophthalmic eye drops administered bilaterally.
The study comprises of a screening and treatment period using the conjunctival allergen challenge model to evaluate TL-925 for the treatment of allergic conjunctivitis.
Enrollment
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Inclusion criteria
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Primary purpose
Allocation
Interventional model
Masking
66 participants in 2 patient groups, including a placebo group
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Central trial contact
Yulia Khalina; John Mei
Data sourced from clinicaltrials.gov
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