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Clinical Trial Summary

To learn about the effects of brentuximab vedotin and pembrolizumab in combination with doxorubicin and dacarbazine when given to patients who have Stage II cHL with bulky mediastinal disease or advanced cHL (Stage III or IV) and who have not received treatment for the disease.


Clinical Trial Description

Primary Objectives: ● To assess the complete response (CR) rate at the end of therapy (EOT) with Brentuximab vedotin and pembrolizumab, doxorubicin and dacarbazine in subject with previously untreated stage II bulky mediastinal disease or advanced stage cHL. Secondary Objectives: - To assess the safety of BvP+AD - To assess the complete remission rate at interim PET (CR iPET) - To assess the overall response rate (ORR) - To assess the duration of response (DOR) - To assess the duration of complete response (DOCR) - To assess event-free survival (EFS) - To assess progression free survival (PFS) - To assess overall survival (OS) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05922904
Study type Interventional
Source M.D. Anderson Cancer Center
Contact Hun Lee, MD
Phone (713) 794-1829
Email hunlee@mdanderson.org
Status Recruiting
Phase Phase 2
Start date December 14, 2023
Completion date October 30, 2025

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