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Clinical Trial Summary

The primary purpose of this study is to assess the safety, tolerability, and pharmacokinetics, and to identify the optimal dose of ADRX-0706 in patients with select advanced solid tumors.


Clinical Trial Description

This is a 2 part study. The Phase 1a will consist of a dose escalation of ADRX-0706 to evaluate initial safety and tolerability in patients with select advanced solid tumors, and to identify the recommended dose to be used in the Phase 1b. The Phase 1b will further evaluate the safety and tolerability, as well as preliminary efficacy, and identify the optimal dose of ADRX-0706 in 3 disease-specific expansion cohorts. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06036121
Study type Interventional
Source Adcentrx Therapeutics
Contact Adcentrx Therapeutics
Phone 858-428-9502
Email clinicaltrials@adcentrx.com
Status Recruiting
Phase Phase 1
Start date September 26, 2023
Completion date December 2026

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