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Home » Directories » FDA Approved Drugs » Zerviate (cetirizine ophthalmic solution 0.24%)

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Zerviate (cetirizine ophthalmic solution 0.24%)

  • Profile

Profile

Contact Information

Contact: Eyevance Pharmaceuticals
Website: https://myzerviate.com/

Currently Enrolling Trials

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    General Information

    Zerviate (cetirizine ophthalmic solution 0.24%) is a second generation antihistamine (H1 receptor antagonist) that binds competitively to histamine receptor sites to reduce swelling, itching and vasodilation. 

    Zerviate is specifically indicated for the treatment of ocular itching associated with allergic conjunctivitis.

    Zerviate is supplied as a solution for topical administration. The recommended dose is one drop in each affected eye twice daily (approximately 8 hours apart).

    Mechanism of Action

    Zerviate (cetirizine ophthalmic solution 0.24%) is a second generation antihistamine (H1 receptor antagonist) that binds competitively to histamine receptor sites to reduce swelling, itching and vasodilation. 

    Side Effects

    Adverse effects associated with the use of Zerviate may include, but are not limited to, the following:

    • ocular hyperemia
    • instillation site pain
    • reduction in visual acuity

    Clinical Trial Results

    The FDA approval of Zerviate was based on three randomized, double-masked, placebo-controlled, conjunctival antigen challenge (Ora-CAC model of allergic conjunctivitis) clinical trials in patients with a history of allergic conjunctivitis. Onset and duration were evaluated in two of these trials in which Zerviate demonstrated statistically and clinically significantly less ocular itching compared to placebo at 15 minutes and 8 hours after treatment.

    Approval Date: 2017-05-01
    Company Name: Eyevance Pharmaceuticals
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