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Epicrispr Biotechnologies to Present at the Upcoming Annual European Society of Gene and Cell Therapy  

SOUTH SAN FRANCISCO, Calif. — October 19, 2023 — Epicrispr Biotechnologies, a biotechnology company developing therapies to modulate gene expression using compact, non-cutting dCas proteins, today announced four poster presentations at the upcoming European Society of Gene and Cell Therapy taking place October 24-27, 2023, in Brussels, Belgium. 

Poster Title: “A Potential Cure for Facioscapulohumeral Muscular Dystrophy (FSHD) Targeting D4Z4 Epigenome” 
Session: Cardiovascular & Muscle Diseases 
Date & Time: October 26, 2023, 8:30-9:30 p.m. CEST 
Poster Number: P605 
Location: Gare Maritime 

Poster Title: “Design and Characterization of Compact and Precise Cas Molecules for Treating Diseases in Patients” 
Session: Gene Editing  
Date & Time: October 26, 2023, 8:30-9:30 p.m. CEST 
Poster Number: P633 
Location: Gare Maritime 

Poster Title: “Discovery and Engineering of Hypercompact Epigenetic Modulators for Durable Activation of Therapeutic Genes” 
Session: Gene Editing 
Date & Time: October 26, 2023, 7:30-9:30 p.m. CEST 
Poster Number: P632 
Location: Gare Maritime 

Poster Title: “Gene Expression Modulation Systems (GEMS): A CRISPR-Based Epigenome Editing Platform for In vivo Therapeutics” 
Session: Gene Editing  
Date & Time: October 26, 2023, 7:30-9:30 p.m. CEST 
Poster Number: P670 
Location: Gare Maritime 

The ESGCT posters will be made available on the Science page of the Epicrispr Biotechnologies website following the conference.  

About Epicrispr Biotechnologies
Epicrispr Biotechnologies is a leading epigenetic editing company, leveraging the power of CRISPR without cutting DNA. The company’s proprietary Gene Expression Modulation System (GEMS) includes the smallest Cas protein known to work in human cells, enabling in vivo delivery via a single AAV vector. Epicrispr’s lead program, EPI-321, is in IND-enabling studies for treatment of facioscapulohumeral muscular dystrophy (FSHD); additional programs seek to address alpha-1 antitrypsin deficiency (A1AD), heterozygous familial hypercholesterolemia (HeFH), and other indications. The company is financially backed by Horizons Ventures and other leading investors. Visit www.epicrispr.com for more information or follow us on Twitter and LinkedIn.

Investor Contact

Shawn M. Cox
Epicrispr Biotechnologies
Manager, Investor Relations, and Corporate Communications
shawn.cox@epic-bio.com

Media Contact

Lisa Raffensperger
Ten Bridge Communications
lisa@tenbridgecommunications.com
(617) 903-8783