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Clinical Trial Summary

This is a Phase 1, open label, non-randomised, dose-escalation single agent study with expansion cohorts for dose confirmation/safety and preliminary efficacy of MCLA-145 in advanced or metastatic malignancies


Clinical Trial Description

Study Design: This open label, multicenter, first in human study consists of 2 parts. Part 1 is a dose escalation to find the recommended dose for the expansion. Part 2 is a dose expansion to confirm the dose of MCLA-145 through further evaluation of safety, tolerability, Pk, preliminary antitumor activity, and functional target engagement. The study includes three periods: Screening( up to 28 days prior to the first dose of study drug); Treatment( first dose of study drug with treatment cycles of 28 days); and Follow-up ( 30 days and 90 days after the last dose) including survival follow-up checks every 2 months up to 12 months after the last dose. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03922204
Study type Interventional
Source Merus N.V.
Contact Gianluca Laus, MD
Phone +31850162500
Email enquires@merus.nl
Status Recruiting
Phase Phase 1
Start date May 8, 2019
Completion date December 2022

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