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12 Oct 2015 Glucocorticoid agonist being developed using Kala Pharmaceuticals US FDA approve EYSUVIS for short-term treatment of dry eye disease.

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Kala Pharmaceuticals has completed their Phase 3 clinical trial, the Short Term Relief of Dry Eye (STRIDE 3) and the medication is now available with a prescription. In this Phase 3 trial, their KPI-121 0.25% loteprednol etabonate ophthalmic suspension was evaluated on safety and effectiveness before hitting the market in early 2021.

The 2020-10-27 January 7, 2021 – Kala Pharmaceuticals has announced the launch of EysuvisTM (loteprednol etabonate ophthalmic suspension), which received U.S. FDA approval on October 26, 2020. Eysuvis is indicated to provide short-term (up to two weeks) treatment of the signs and symptoms of dry eye disease (DED). The product is the first ocular steroid to be FDA approved specifically for DED. Kala Pharmaceuticals announced today that the U.S. Food and Drug Administration (FDA) has approved EYSUVIS for the short-term treatment of dry eye disease. Roughly 16.4 million U.S. adults have been diagnosed with dry eye disease, a chronic, episodic, multifactorial disease.

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There are several reasons tears might be inadequate. Dry eyes occur when an individual's tears don't lubricate their eyes well enough. There are several reaso Symptoms of dry eye include burning, redness, excessive tearing, and the sensation that you have something stuck in your eye.
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8 Feb 2021 Eysuvis is a low dose topical steroid intended for short term use in the treatment of dry eye disease by Kala Pharmaceuticals. Tune in LIVE as 27 Oct 2020 Prior to Eysuvis, there were no FDA-approved ocular corticosteroids for the treatment of dry eye disease.

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Kala Pharmaceuticals Resubmits New Drug Application for Eysuvis for Dry Eye Disease - May 4, 2020 Kala Pharmaceuticals Receives FDA Complete Response Letter for KPI-121 0.25% NDA and Plans to Respond with Data From STRIDE 3 Trial - August 8, 2019

Both articl 24 Dec 2020 dry eye disease (DED)—loteprednol etabonate ophthalmic suspension 0.25% (Eysuvis; Kala Pharmaceuticals)—has received FDA approval, 15 Mar 2021 AbbVie Inc; Bausch + Lomb Inc; Kala Pharmaceuticals; Novartis; Oyster Point Market research interviews on dry eye disease (blinded). 8 Feb 2021 Eysuvis is a low dose topical steroid intended for short term use in the treatment of dry eye disease by Kala Pharmaceuticals. Tune in LIVE as 27 Oct 2020 Prior to Eysuvis, there were no FDA-approved ocular corticosteroids for the treatment of dry eye disease. Kala plans to launch the product in the The smoking-cessation drug, reformulated for nasal delivery, could be launched for dry eye, Oyster Point hopes. Article image. Vantage logo.

In this Phase 3 trial, their KPI-121 0.25% loteprednol etabonate ophthalmic suspension was evaluated on safety and effectiveness before hitting the market in early 2021. 🔴 There is an exciting new medication on the horizon for dry eye sufferers, and it is specifically targeted at acute flare-ups of the condition. Eysuvis is ~90% of surveyed dry eye patients experience flares and the majority have multi-day episodes1 1 Kala survey of 503 diagnosed dry eye patients, December 2017 2 Source for dry eye disease market data: Epidemiology research commissioned by Kala and performed by a third party Kala survey of 503 diagnosed dry eye patients, December 2017 2 Source for dry eye disease market data: Epidemiology research commissioned by Kala and performed by a third party Eysuvis 0.25% is the first and only approved prescription therapy for short-term treatment of signs and symptoms related to dry eye disease. In January, Eysuvis (loteprednol etabonate ophthalmic suspension) 0.25% for dry eye disease launched across the US in national and regional pharmaceutical distribution centers.