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Clinical Trial Summary

Phase 1 (Dose Escalation) of this study will assess the safety, tolerability, dose-limiting toxicity (DLT), and will determine the maximum tolerated dose (MTD) and recommended Phase 2 dose (RP2D) of EU101 in participants with advanced solid tumors. Phase 2 (Dose Expansion) of the study will assess the antitumor effect of EU101 in two indications including colorectal cancer (CRC) and non-small cell lung cancer (NSCLC).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04903873
Study type Interventional
Source Eutilex
Contact Seoyoun Kim, MPH
Phone 82-10-4227-0925
Email s.kim@eutilex.com
Status Recruiting
Phase Phase 1/Phase 2
Start date May 31, 2021
Completion date December 2025

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