Abeona Therapeutics To Present At The 18th Annual BIO CEO & Investor Conference

DALLAS, TX and NEW YORK, NY--(Marketwired - February 04, 2016) - Abeona Therapeutics, Inc. (ABEO), a biopharmaceutical company focused on developing and delivering gene therapy and plasma-based products for severe and life-threatening rare diseases, today announced that Jeffrey Davis, COO, will be presenting for the company at the Annual BIO CEO & Investor Conference in New York City, NY on Monday, February 8th, 2016 at 4pm EST in The Duke of Windsor Room at The Waldorf Astoria.

Event: BIO CEO and Investor Conference
Date: Monday, February 8th, 2016
Time: 4:00pm EST
Location: The Waldorf Astoria, New York City
Room: Duke of Windsor
Webcast Link: http://www.veracast.com/webcasts/bio/ceoinvestor2016/97132155761.cfm

The presentation will be open to all interested investors through a live audio webcast accessible from http://www.veracast.com/webcasts/bio/ceoinvestor2016/97132155761.cfm.

An archived replay of the webcast will also be available for 90 days following the live presentation.

About BIO:

The BIO CEO & Investor Conference is one of the largest investor conferences focused on established and emerging publicly traded and select private biotech companies. Each year the BIO CEO & Investor Conference provides a neutral forum where institutional investors, industry analysts, and senior biotechnology executives have the opportunity to shape the future investment landscape of the biotechnology industry.

About Abeona:

Abeona Therapeutics, Inc. develops and delivers gene therapy and plasma-based products for severe and life-threatening rare diseases. Abeona's lead programs are AB0-101 (AAV NAGLU) and ABO-102 (AAV SGSH), adeno-associated virus (AAV)-based gene therapies for Sanfilippo syndrome (MPS IIIB and IIIA). We are also developing ABO-201 (AAV CLN3) gene therapy for juvenile Batten disease (JBD); and ABO-301 (AAV FANCC) for Fanconi anemia (FA) disorder using a novel CRISPR/Cas9-based gene editing approach to gene therapy program for rare blood diseases. In addition, we are also developing rare plasma protein therapies including SDF Alpha™ (alpha-1 protease inhibitor) for inherited COPD using our proprietary SDF™ (Salt Diafiltration) ethanol-free process. For more information, visit www.abeonatherapeutics.com.

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