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Clinical Trial Summary

This study will be conducted to evaluate the safety, tolerability, cellular kinetics (CK), activity, and pharmacodynamics (PD) of NTLA-5001 in participants with Acute Myeloid Leukemia (AML).


Clinical Trial Description

This 2-part first in human (FIH) study is comprised of two open-label arms. It is a multi-center, Phase 1/2a study evaluating the safety and activity of NTLA-5001 in subjects with persistent or recurrent Acute Myeloid Leukemia after first-line or later therapy. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05066165
Study type Interventional
Source Intellia Therapeutics
Contact Trial Manager at Intellia
Phone 833-888-0387
Email [email protected]
Status Not yet recruiting
Phase Phase 1/Phase 2
Start date October 2021
Completion date September 2025

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