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Clinical Trial Summary

The primary purpose of the study is to assess safety, and to identify the recommended phase 2 dose (RP2D) of tolinapant in combination with oral decitabine/cedazuridine in Phase 1 and to assess preliminary efficacy as determined by overall response rate (ORR) in Phase 2.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05403450
Study type Interventional
Source Astex Pharmaceuticals, Inc.
Contact
Status Active, not recruiting
Phase Phase 1/Phase 2
Start date June 23, 2022
Completion date December 1, 2026

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