EyePoint’s Yutiq is indicated to treat chronic non-infectious uveitis which affects the posterior segment of the eye. Credit: fizkes via Shutterstock.com.

Alimera Sciences has acquired the US commercialisation rights for Yutiq (fluocinolone acetonide intravitreal implant) 0.18mg from EyePoint Pharmaceuticals.

Yutiq is indicated to treat chronic, non-infectious uveitis that affects the posterior segment of the eye.

Go deeper with GlobalData

Data Insights

The gold standard of business intelligence.

Find out more

Related Company Profiles

View all

It received approval from the US Food and Drug Administration in October 2018.

Alimera Sciences has exclusive global rights to Yutiq excluding Southeast Asia, Hong Kong, Macau, China and South Korea, where the therapy was previously licensed to Ocumension Therapeutics.

The company made a $75m up-front cash payment to EyePoint Pharmaceuticals on the closure of the deal, and an additional $7.5m will be paid in equal quarterly instalments in 2024.

EyePoint Pharmaceuticals will also receive potential royalties on the combined net sales of Iluvien and Yutiq in the US from 2025 to 2028.

How well do you really know your competitors?

Access the most comprehensive Company Profiles on the market, powered by GlobalData. Save hours of research. Gain competitive edge.

Company Profile – free sample

Thank you!

Your download email will arrive shortly

Not ready to buy yet? Download a free sample

We are confident about the unique quality of our Company Profiles. However, we want you to make the most beneficial decision for your business, so we offer a free sample that you can download by submitting the below form

By GlobalData
Visit our Privacy Policy for more information about our services, how we may use, process and share your personal data, including information of your rights in respect of your personal data and how you can unsubscribe from future marketing communications. Our services are intended for corporate subscribers and you warrant that the email address submitted is your corporate email address.

EyePoint Pharmaceuticals CEO Nancy Lurker stated: “This transaction completes EyePoint’s transformation into a pure play drug development company focused on advancing and expanding a pipeline of sustained delivery treatments for serious eye diseases, including our lead product candidate EYP-1901, currently in Phase II trials in wet age-related macular degeneration and non-proliferative diabetic retinopathy.

“This value-creating transaction has enabled EyePoint to pay off all outstanding bank debt at closing, reduce our projected selling, general and administrative spending and extend our cash runway into 2025 as we prepare for the potential Phase III pivotal trials for EYP-1901.”

EYP-1901 is an investigational sustained delivery intravitreal anti-VEGF treatment which is now being evaluated in Phase II clinical trials.

It provides steady blocking of VEGFR to prevent loss of vision and neovascularisation.