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Clinical Trial Summary

This study evaluates TL-895, a tyrosine kinase inhibitor (TKI). This is a study comprising a Phase 1 safety assessment. TL-895 open-label will be administered orally at an assigned dose continuously in 7-day cycles for 2 cycles. Up to 3 dose levels will be evaluated. Only Phase 1 of the study was enrolled and the study did not proceed into Phase 2.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04419623
Study type Interventional
Source Telios Pharma, Inc.
Contact
Status Completed
Phase Phase 1
Start date July 9, 2020
Completion date December 15, 2020

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