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Clinical Trial Summary

This first-in-human study will evaluate RVU120 (SEL120), a novel small molecule CDK8/19 inhibitor, in patients with Acute Myeloid Leukemia (AML) or High-risk Myelodysplastic Syndrome (HR-MDS), in terms of selection of the recommended dose for further clinical development and assessment of safety, tolerability, preliminary anti-leukemic activity, as well as pharmacokinetic and pharmacodynamic profiles.


Clinical Trial Description

The study will determine the recommended phase II dose (RP2D) and safety of RVU120 (SEL120) given as monotherapy over a range of dose-levels, following a closely controlled dose escalation study design. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04021368
Study type Interventional
Source Ryvu Therapeutics SA
Contact
Status Active, not recruiting
Phase Phase 1
Start date September 4, 2019
Completion date December 30, 2024

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