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Arno’s investigational new drug application for tumor drug accepted by FDA

Arno Therapeutics, a clinical-stage biopharmaceutical company, has reported that the FDA has accepted the company's investigational new drug application for the use of AR-42.

AR-42 is an orally available, novel, potent, small molecule that modifies the acetylation of histones and other molecules, and is a targeted inhibitor of the Pan-DAC and Akt pathways. Arno in-licensed the exclusive worldwide rights to AR-42 from The Ohio State University.

In preclinical studies, AR-42 has demonstrated greater potency and a competitive profile in tumors when compared with vorinostat (also known as SAHA and marketed as Zolina by Merck), the leading marketed histone deacetylase inhibitor, said Arno.