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TheraSphere With Durvalumab and Tremelimumab for HCC

Active, not recruiting · Phase 2 · NCT05063565

Conditions: Hepatocellular Carcinoma

At a glance

Research payments reported, 2025
$1.7M
U.S. investigators named
15
Sites paid
15
Planned or actual enrollment
100

About the trial

Sponsor
Boston Scientific Corporation (with Biocompatibles UK Ltd)
Tested
TheraSphere Y-90 glass microsphere therapy (device), Durvalumab (Imfinzi) immunotherapy (drug), Tremelimumab immunotherapy (drug)
Dates
Started 2023-11-03; completion 2027-06
Results posted
Not yet

The objective of the ROWAN clinical study is to assess the efficacy of local tumor control in HCC patients who receive TheraSphere followed by durvalumab and tremelimumab.

From ClinicalTrials.gov, last updated 2026-10-30. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Boston Scientific Corporation reported $1.7M in research payments for this study in 2025 (114 payments).

Products named: Clinical Trial Product

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.