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Clinical Trial Summary

Phase 1 study to evaluate safety, tolerability and anti-tumor activity of RGT-61159 in patients with ACC or CRCT


Clinical Trial Description

This first-in-human, Phase 1, multi-center, open-label, non-randomized study, is designed to evaluate safety, tolerability, and anti-tumor activity of once-daily RGT-61159 in patients with advanced R/R ACC or R/R CRC for whom standard therapy with proven clinical benefit does not exist, is no longer effective, or is not appropriate. RGT-61159 is an oral, small molecule MYB inhibitor. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06462183
Study type Interventional
Source Rgenta Therapeutics Inc
Contact Clinical Operations
Phone 857-225-2840
Email Clinical-Operations@rgentatx.com
Status Not yet recruiting
Phase Phase 1
Start date June 2024
Completion date June 2027

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