PolyActiva Pty Ltd.
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LatanoprostModel FA SR - Ocular Implant

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Being developed to reduce IOP caused by Open-Angle Glaucoma & Ocular Hypertension. Clinical Investigation Stage: Phase II.

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Micro implant. Sustained drug release.

The Target Product Profile for the Latanoprost FA SR Ocular Implant, currently under development, aims to deliver the following clinical benefits:

PolyActiva achieved study objectives in completed clinical study (NCT03604328) and interim analysis of ongoing study NCT04060758. The Latanoprost FA SR Ocular implant has not been approved by the U.S. Food and Drug Administration (FDA).