FDA Clears IND Application for RGT-61159 in CRC & Adenoid Cystic Carcinoma (ACC)
“Clearance of our first IND application is a significant milestone in Rgenta’s mission to develop oral, small molecule RNA-targeting medicines to treat previously incurable diseases,” said Simon Xi, Ph.D., co-founder and chief executive officer of Rgenta. “We look forward to initiating clinical studies of RGT-61159 with a first-in-human Phase1a/1b clinical study in adults with ACC and CRC to potentially provide a new therapeutic option for patients with these difficult-to-treat cancers.”
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