Study identifier:D419CR00035
ClinicalTrials.gov identifier:NCT06252753
EudraCT identifier:N/A
CTIS identifier:N/A
An Observational Multi-Center Study to Evaluate Real-World Treatment Outcomes With or Without Durvalumab-Based Regimens in Hepatobiliary Cancers
Hepatobiliary Cancers
Phase 4
No
-
All
4000
Observational
18 Years - 130 Years
Allocation: N/A
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Sept 2026 by AstraZeneca
AstraZeneca
ICON plc
No locations available
| Arms | Assigned Interventions |
|---|---|
| unresectable hepatocellular carcinoma (uHCC) advanced uHCC patients who had not received prior systemic therapy and were not eligible for LRT, as well as those who had progressed following LRT, and who have received a durvalumab-based regimen | Other: Durvalumab-based combination therapies in observational study setting Data on patients who initiated durvalumab-based regimens, including STRIDE (Single Tremelimumab Regular Interval Durvalumab), will be collected). Other Name: Imfinzi |
| advanced biliary tract cancer (aBTC) patients with advanced BTC (aBTC) who are not eligible for resection and who have received a durvalumab-based regimen | Other: Durvalumab-based combination therapies in observational study setting Data on patients who initiated durvalumab-based regimens, including durvalumab + chemotherapy combinations (e.g., Durvalumab + GemCis etc.) will be collected. Other Name: Imfinzi |
| eeHCC uHCC patients with liver-confined disease not amenable to curative treatment but amenable to LRT who receive LRT alone or LRT followed by systemic therapy within 60 days (if administered in combination, LRT must be received first) | Other: Non Durvalumab-based therapies in observational study setting Data on patients who initiated non durvalumab-based regimens, including LRT alone or LRT followed by systemic therapies, will be collected. |
| EMERALD uHCC patients with liver-confined disease not amenable to curative treatment but amenable to LRT who receive durvalumab-based regimens in combination with LRT (durvalumab and LRT are given within 28 days of each other, regardless of order) | Other: Durvalumab-based combination therapies in observational study settings Data on patients who initiated durvalumab-based regimens in combination with LRT, will be collected Other Name: Imfinzi |