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Clinical Trial Summary

This is an open-label, non-randomized, multicenter, dose-escalation and expansion study in patients with selected solid tumors.


Clinical Trial Description

This study will determine the maximum tolerated dose of CDX-585 while also evaluating the safety, tolerability, and efficacy of CDX-585 in patients with cancer. Eligible patients that enroll to the dose-escalation portion of the study will be assigned to one of several dose levels of CDX-585. The dose-escalation part of the study will test the safety profile of CDX-585 and determine which dose of CDX-585 will be studied in the expansion portions of the study. Approximately 130 patients will be enrolled. All patients enrolled in the study will be closely monitored to determine if there is a response to the treatment as well as for any side effects that may occur. The expansion portion of the study will further evaluate the safety of CDX-585 in selected tumor types at the dose level chosen during the escalation part of the study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05788484
Study type Interventional
Source Celldex Therapeutics
Contact Celldex Therapeutics
Phone (844) 723-9363
Email info@celldex.com
Status Recruiting
Phase Phase 1
Start date May 11, 2023
Completion date February 2026

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