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Clinical Trial Summary

The purpose of this study is to determine whether the combination of subcutaneous DRP-104 in combination with intravenous Durvalumab is safe and yields a clinically compelling antitumor activity measured as based on objective response rate (ORR, assessed by RECIST 1.1). Secondary objectives include progression-free survival (PFS) and overall survival (OS).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06027086
Study type Interventional
Source Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Contact Colleen Apostal, RN
Phone 410-614-3644
Email GIClinicalTrials@jhmi.edu
Status Recruiting
Phase Phase 1/Phase 2
Start date February 6, 2024
Completion date February 1, 2027

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