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Clinical Trial Summary

The primary objective of this study is to assess the safety and tolerability of E7386 in participants with solid tumor including CRC.


Clinical Trial Description

The study will be conducted in 3 parts: dose escalation part, expansion part 1 and expansion part 2. The study will include Pre-treatment Phase, Treatment Phase, and Extension Phase (in expansion parts only). Eligible participants from Pre-Treatment Phase (screening period) will enter into the Treatment Phase to receive E7386. After Treatment Phase, participants will be followed in follow-up period of Extension Phase (in expansion parts only). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03833700
Study type Interventional
Source Eisai Inc.
Contact
Status Active, not recruiting
Phase Phase 1
Start date March 5, 2019
Completion date March 31, 2025

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