US genetic medicines firm Arbor Biotechnologies has announced the closing of a $73.9 million Series C financing to support the advancement of its pipeline of novel gene editing therapeutics targeting diseases in the liver and central nervous system (CNS).
Proceeds will support clinical development of the company’s lead therapeutic candidate, ABO-101, in primary hyperoxaluria type 1 (PH1) and progression to IND/CTA filing of its programs, including an RT editing program for a rare liver disease and a program targeting amyotrophic lateral sclerosis.
Arbor explains that its pipeline is built upon a suite of proprietary, wholly-owned genomic editors that enable a variety of functions, unlocking sophisticated and precise ways of editing the genome that offer unique properties, high specificity and broad therapeutic applications.
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