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Clinical Trial Summary

The objective of the ROWAN clinical study is to assess the the durability of local tumor control in HCC patients who receive TheraSphere followed by durvalumab and tremelimumab, compared to those who receive TheraSphere treatment alone.


Clinical Trial Description

A global open-label, prospective, multi-center, randomized, Phase II trial with two treatment arms designed to assess the safety and efficacy of TheraSphere administered before initiation of Durvalumab with Tremelimumab in HCC patients not eligible for or who have declined curative treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05063565
Study type Interventional
Source Boston Scientific Corporation
Contact Michelle Wells
Phone 763-494-1883
Email [email protected]
Status Not yet recruiting
Phase Phase 2
Start date December 2021
Completion date June 2025

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