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Clinical Trial Summary

This interventional study will evaluate the efficacy and safety of ART0380 as monotherapy in patients whose tumors have a biology to predict for sensitivity to inhibition of Ataxia-Telangiectasia Mutated and Rad3-related protein kinase (ATR).


Clinical Trial Description

ART0380 is being developed as an oral anti-cancer agent for the treatment of patients with cancers that have defects in deoxyribonucleic acid (DNA) repair. The study will recruit selected patients with advanced or metastatic solid tumors, specifically: - Patients with persistent or recurrent endometrial cancer (EC) - Patients with advanced or metastatic solid tumors of any histology Above patients will be randomized in a 1:1 ratio to one of two dose regimens of ART0380. Safety will be evaluated on a quarterly basis, at a minimum. Patients may continue to receive ART0380 as long as they are continuing to derive benefit from treatment or until disease progression, withdrawal of consent, or until they experience unacceptable drug-related toxicity. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05798611
Study type Interventional
Source Artios Pharma Ltd
Contact Artios Pharma
Phone +44 (0)1223 867 900
Email info@artios.com
Status Recruiting
Phase Phase 2
Start date September 6, 2023
Completion date March 2025

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