First Patient dosed in the RIVER-52 Phase II Study of RVU120 Monotherapy for the Treatment of Patients with R/R AML and HR-MDS
Hendrik Nogai, M.D., Chief Medical Officer of Ryvu Therapeutics, said, “We are pleased to announce the initiation of another RVU120 Phase II study, in line with the development plans presented last year. Based on the demonstrated safety profile and observed signs of activity from the Phase Ib study in patients with r/r AML or HR-MDS, we continue to be at the forefront of developing first-in-class CDK8/19 inhibitors. This marks a significant step towards our goal of effectively treating various hematological diseases and providing therapeutic options for patients with unmet medical needs.”
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