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ALPHARETTA, Ga., Oct. 19, 2018 (GLOBE NEWSWIRE) — Clearside Biomedical, Inc. (NASDAQ:CLSD), a biopharmaceutical aggregation committed to developing treatments that restore and bottle eyes for bodies with austere eye diseases, today appear the arrangement of Thomas Crawford, CSCP, as Vice President, Accumulation Chain.

Mr. Crawford will be amenable for establishing and managing Clearside’s all-around accumulation alternation for analytic testing, training and, if approved, barter administering of suprachoroidal CLS-TA, the company’s proprietary abeyance of the corticosteroid triamcinolone acetonide formulated for administering to the aback of the eye via the suprachoroidal space.  

In a career spanning added than 25 years, Mr. Crawford has all-encompassing ability in accumulation alternation management, barter relations, artefact launches, and accomplishment operations.  Before aing Clearside, he was Vice President of Accumulation Alternation and Customer Service for Pharma Tech Industries, LLC, the world’s better biologic arrangement architect and packager of crumb products.  Mr. Crawford’s beforehand acquaintance includes accumulation chain, accomplishment and barter relations administration roles at assorted biologic and medical accessory companies, including Shionogi Inc., Immucor Inc., Aronex Pharmaceuticals Inc., Allergan, Inc., Abbot Laboratories and Zenith Goldline Pharmaceuticals, Inc.

“Thomas brings an important abyss of accomplishment operations and accumulation alternation administration acquaintance to the company,” said Clearside’s Chief Executive Officer and President, Daniel White.  “Thomas will be in a position to accommodate seamless administering administration for suprachoroidal CLS-TA to abounding of our all-around testing sites and, if suprachoroidal CLS-TA is approved, in abutment of our bartering supply.”

About Clearside

Clearside Biomedical, Inc. is a biopharmaceutical aggregation committed to developing treatments that restore and bottle eyes for bodies with austere eye diseases.  Clearside’s proprietary suprachoroidal analysis admission offers aberrant admission to the aback of the eye area sight-threatening ache generally occurs.  The company’s different belvedere for eye ache treatments is inherently adjustable and advised to assignment with accustomed medicines, new formulations of medicines, as able-bodied as approaching innovations.  Clearside’s activity includes avant-garde and pre-clinical artefact candidates in diseases area macular edema is a accepted complication, including uveitis, retinal attitude occlusion (“RVO”) and diabetic macular edema (“DME”).  Clearside’s best avant-garde affairs is in non-infectious uveitis and it expects to abide a New Drug Application (“NDA”) to the U.S. Food and Drug Administering (“FDA”) for use of suprachoroidal CLS-TA for the analysis of macular edema associated with non-infectious uveitis by the end of 2018.  The aggregation is additionally administering two advancing Phase 3 trials of suprachoroidal CLS-TA with an intravitreal anti-VEGF abettor in patients with RVO.  In addition, Clearside afresh appear absolute topline after-effects from a Phase 2 analytic balloon of suprachoroidal CLS-TA acclimated with Eylea® (aflibercept) in patients with DME, and is continuing to assay added abstracts from the balloon as it becomes available.  Clearside  is headquartered in Alpharetta, GA.  For added information, amuse appointment http://www.clearsidebio.com.  Follow @clearsidebio on Twitter and Linkedin.

Cautionary Note Apropos Forward-Looking Statements

Any statements independent in this columnist absolution that do not call absolute facts may aggregate advanced statements as that appellation is authentic in the Private Securities Litigation Reform Act of 1995.  These statements may be articular by words such as “believe”, “expect”, “may”, “plan”, “potential”, “will”, and agnate expressions, and are based on Clearside’s accepted behavior and expectations. These advanced statements accommodate expectations apropos the analytic development of Clearside’s artefact candidates, and the timing of a abeyant acquiescence of an NDA with the FDA. These statements absorb risks and uncertainties that could account absolute after-effects to alter materially from those reflected in such statements. Risks and uncertainties that may account absolute after-effects to alter materially accommodate uncertainties inherent in the conduct of analytic trials, Clearside’s assurance on third parties over which it may not consistently accept abounding control, and added risks and uncertainties that are declared in Clearside’s Annual Report on Form 10-K for the year concluded December 31, 2017, filed with the U.S. Securities and Exchange Commission (“SEC”) on March 16, 2018, and Clearside’s added Periodic Reports filed with the SEC.  Any advanced statements allege alone as of the date of this columnist absolution and are based on advice accessible to Clearside as of the date of this release, and Clearside assumes no obligation to, and does not intend to, amend any advanced statements, whether as a aftereffect of new information, approaching contest or otherwise.

Contacts:

Stephen KilmerInvestor Relations(678) [email protected]

Charles DeignanChief Financial Officer(678) [email protected]

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