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Clinical Trial Summary

This is a phase 1, non-randomized open-label, multicenter platform study designed to evaluate the tolerability and safety of AB122 in patients with malignancies specified in each cohort.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04999761
Study type Interventional
Source Taiho Pharmaceutical Co., Ltd.
Contact Drug Information Center
Phone +81-3-3294-4527
Email toiawase@taiho.co.jp
Status Recruiting
Phase Phase 1
Start date June 1, 2021
Completion date May 2026

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