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Clinical Trial Summary

This is a Phase I open label multi-center study to evaluate the safety, tolerability, pharmacokinetics and preliminary effectiveness of the investigational drug MYTX-011 in patients with locally advanced, recurrent or metastatic NSCLC. MYTX-011 is in a class of medications called antibody drug conjugates (ADCs). MYTX-011 is composed of a pH-dependent anti-cMET antibody and the potent antimicrotubule drug monomethyl auristatin E (MMAE).


Clinical Trial Description

The study will be conducted in 2 parts. Part 1 will assess the safety and tolerability of MYTX-011 and identify the dose to be studied in Part 2. Part 2 will include subjects with NSCLC with cMET overexpression or MET amplification/exon 14 skipping mutations, populations with a current unmet medical need. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05652868
Study type Interventional
Source Mythic Therapeutics
Contact William T Downing
Phone 1-833-888-1138
Email clinicalsupport@mythictx.com
Status Recruiting
Phase Phase 1
Start date March 23, 2023
Completion date December 2027

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